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        <title>Roche Investor Update via MedWorm.com</title>
        <description>MedWorm.com provides a medical RSS filtering service. Over 6000 RSS medical sources are combined and output via different filters. This feed contains the latest items from the 'Roche Investor Update' source.</description>
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        <lastBuildDate>Sat, 20 Mar 2010 15:04:18 +0100</lastBuildDate>
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            <title>Roche uniquely positioned to deliver long-term growth</title>
            <link>http://www.medworm.com/index.php?rid=3376457&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Finvestors%2Fir_update%2Finv-update-2010-03-18.htm</link>
            <description>Leading late-stage pipeline and innovation strategy presented at investor conference. Roche is set to strengthen its global leadership position in oncology and to expand in therapeutic areas such as metabolism, inflammation and diseases of the central nervous system. At its first investor conference following the successful integration of Roche and Genentech, the company highlighted its vision and the strategy that it intends to pursue in order to ensure a stable flow of novel medicines from its rich development pipeline. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
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            <pubDate>Thu, 18 Mar 2010 06:00:00 +0100</pubDate>
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            <title>ACTEMRA(tocilizumab) filed in the US for Prevention of Structural Joint Damage and Improvement of Physical Function in Rheumatoid Arthritis</title>
            <link>http://www.medworm.com/index.php?rid=3372420&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Finvestors%2Fir_update%2Finv-update-2010-03-17.htm</link>
            <description>Roche announced today that it has submitted a supplemental Biologics License Application (sBLA) to the United States (US) Food and Drug Administration (FDA) for ACTEMRA (tocilizumab, RoACTEMRA in the European Union) for the prevention of structural joint damage and to improve physical function in adults with moderately to severe active rheumatoid arthritis (RA). ACTEMRA was approved by the FDA on January 8, 2010 as the first interleukin-6 (IL-6) receptor-inhibiting monoclonal antibody to treat RA in adult patients after an inadequate response to at least one other medicine called a tumor necrosis factor (TNF) antagonist. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
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            <pubDate>Wed, 17 Mar 2010 06:00:00 +0100</pubDate>
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            <title>Roche&amp;#039;s First Quarter Sales 2010 Conference Call</title>
            <link>http://www.medworm.com/index.php?rid=3365098&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Finvestors%2Fir_update%2Finv-update-2010-03-15.htm</link>
            <description>Roche will publish its Sales Results for the 1st Quarter of 2010 prior to the opening of the Swiss Stock Exchange on Thursday April 15th, 2010. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
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            <pubDate>Mon, 15 Mar 2010 09:00:00 +0100</pubDate>
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            <title>Roche provides update on phase III study of Avastin in men with late stage prostate cancer</title>
            <link>http://www.medworm.com/index.php?rid=3356883&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Finvestors%2Fir_update%2Finv-update-2010-03-12.htm</link>
            <description>Roche announced today the topline results of a phase III trial led by the US Cancer and Leukemia Group B (CALGB) and sponsored by the National Cancer Institute investigating the use of Avastin (bevacizumab) in combination with docetaxel chemotherapy and prednisone in men with late stage prostate cancer (hormone-refractory / HRPC). The study, known as CALGB 90401, did not meet its primary objective of extending overall survival compared to chemotherapy and prednisone alone. A preliminary assessment of safety performed by CALGB has shown adverse events that have been previously observed in pivotal trials with Avastin. Data from the study will be submitted by CALGB for presentation at the 2010 American Society of Clinical Oncology (ASCO) annual meeting, June 4 to 8, 2010. (Source: Roche Inves...</description>
            <author>Roche Investor Update</author>
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            <pubDate>Fri, 12 Mar 2010 06:00:00 +0100</pubDate>
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            <title>Roche and Biogen Idec decide to suspend Ocrelizumab treatment -  Rheumatoid Arthritis development programme on hold</title>
            <link>http://www.medworm.com/index.php?rid=3341014&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Finvestors%2Fir_update%2Finv-update-2010-03-08.htm</link>
            <description>Roche and Biogen Idec announced today their decision to suspend Ocrelizumab treatment of patients in the Rheumatoid Arthritis (RA) programme. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
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            <pubDate>Mon, 08 Mar 2010 06:00:00 +0100</pubDate>
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            <title>Roche Annual General Meeting: dividend raised by 20%</title>
            <link>http://www.medworm.com/index.php?rid=3320450&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Finvestors%2Fir_update%2Finv-update-2010-03-02.htm</link>
            <description>Roche&amp;#039;s Annual General Meeting, which was held today in Basel, has approved all the Board of Directors&amp;#039; proposals. The 698 shareholders in attendance, representing 143,055,648, or 89.4% of a total of 160,000,000 bearer shares, approved the 2009 Annual Report and financial statements. They also authorised a +20% increase in the dividend to 6.00 Swiss francs per share and non-voting equity. With this increase, the payout ratio rises to 53%, which means that about half of net income will be paid out to shareholders. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
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            <pubDate>Tue, 02 Mar 2010 12:30:00 +0100</pubDate>
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            <title>Avastin phase III study shows positive results in women with advanced ovarian cancer</title>
            <link>http://www.medworm.com/index.php?rid=3304810&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Finvestors%2Fir_update%2Finv-update-2010-02-25.htm</link>
            <description>Roche announced today that a phase III study showed the combination of Avastin (bevacizumab) and chemotherapy followed by maintenance use of Avastin increased the time women with advanced ovarian cancer lived without their disease worsening (progression-free survival or PFS) compared to chemotherapy alone. A preliminary assessment of safety noted adverse events previously observed in pivotal trials with Avastin. Data from the study will be submitted for presentation at the 2010 American Society of Clinical Oncology (ASCO) annual meeting, June 4 to 8, 2010. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
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            <pubDate>Thu, 25 Feb 2010 06:00:00 +0100</pubDate>
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            <title>European Medicines Agency grants positive opinion for Xeloda in combination with oxaliplatin for the adjuvant treatment of early colon cancer</title>
            <link>http://www.medworm.com/index.php?rid=3300400&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Finvestors%2Fir_update%2Finv-update-2010-02-24.htm</link>
            <description>Roche announced today that Xeloda (capecitabine) in combination with oxaliplatin (a combination known as XELOX) has been recommended by the Committee on Human Medicinal Products (CHMP) for the adjuvant (post-surgery) treatment of patients with early colon cancer. The CHMP positive recommendation was based on results from the phase III pivotal NO16968 (XELOXA) study, one of the largest studies of patients with stage III (early) colon cancer, which showed that patients taking XELOX immediately after surgery lived disease-free for longer compared to those treated with the chemotherapy regimen 5-fluorouracil/leucovorin (5-FU/LV). (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
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            <pubDate>Wed, 24 Feb 2010 06:00:00 +0100</pubDate>
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            <title>Phase III study of Avastin plus chemotherapy in advanced stomach cancer did not meet primary endpoint</title>
            <link>http://www.medworm.com/index.php?rid=3296769&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Finvestors%2Fir_update%2Finv-update-2010-02-23.htm</link>
            <description>Roche announced today the topline results from a global phase III trial investigating the use of Avastin (bevacizumab) in combination with Xeloda (capecitabine) or fluorouracil and cisplatin chemotherapy in patients with inoperable, advanced or metastatic gastric cancer (stomach cancer). The study, known as AVAGAST, did not meet its primary endpoint of extending overall survival in patients treated with Avastin in combination with chemotherapy compared to the same chemotherapy plus placebo. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
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            <pubDate>Tue, 23 Feb 2010 06:00:00 +0100</pubDate>
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            <title>US FDA approves Rituxan/MabThera for the most common type of adult leukemia</title>
            <link>http://www.medworm.com/index.php?rid=3296770&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Finvestors%2Fir_update%2Finv-update-2010-02-19.htm</link>
            <description>Roche announced today that the US Food and Drug Administration (FDA) approved Rituxan/MabThera (rituximab) plus fludarabine and cyclophosphamide (FC) chemotherapy for people with either previously untreated (first-line) or previously treated (relapsed or refractory) CD20-positive chronic lymphocytic leukemia (CLL). (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
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            <pubDate>Fri, 19 Feb 2010 06:00:00 +0100</pubDate>
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            <title>Strong operating performance for Roche in 2009</title>
            <link>http://www.medworm.com/index.php?rid=3296771&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Finvestors%2Fir_update%2Finv-update-2010-02-03.htm</link>
            <description>Record sales, double-digit growth in operating profit and Core Earnings per share &amp;#8211; Dividend increase by 20% to 6.00 Swiss francs proposed - Group sales increase by 10% to 49.1 billion Swiss francs (8% in Swiss francs, 7% in US dollars). Both divisions gain market share. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
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            <pubDate>Wed, 03 Feb 2010 06:00:00 +0100</pubDate>
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            <title>Roche establishes new medical research hub in Singapore</title>
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            <description>Roche announced today that it will enter into a strategic alliance with Singapore&amp;#8217;s scientific and medical institutions to set up a major new translational research hub in Singapore. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
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            <pubDate>Thu, 28 Jan 2010 06:00:00 +0100</pubDate>
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            <title>Herceptin now approved in the EU for patients with HER2-positive advanced stomach cancer</title>
            <link>http://www.medworm.com/index.php?rid=3296772&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Finvestors%2Fir_update%2Finv-update-2010-01-28.htm</link>
            <description>Roche announced today that the European Commission has approved Herceptin (trastuzumab) in combination with chemotherapy for use in patients with HER2-positive metastatic stomach (gastric) cancer. The approval is based on the impressive results from the international ToGA trial, which showed that treatment with Herceptin significantly prolongs the lives of patients with this aggressive cancer. (Source: Roche Investor Update)</description>
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            <pubDate>Thu, 28 Jan 2010 06:00:00 +0100</pubDate>
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            <title>Roche establishes new medical research hub in Singapore</title>
            <link>http://www.medworm.com/index.php?rid=3214790&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2010-01-28b.htm</link>
            <description>Roche announced today that it will enter into a strategic alliance with Singapore&amp;#8217;s scientific and medical institutions to set up a major new translational research hub in Singapore. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
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            <pubDate>Thu, 28 Jan 2010 06:00:00 +0100</pubDate>
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            <title>Herceptin now approved in the EU for patients with HER2-positive advanced stomach cancer</title>
            <link>http://www.medworm.com/index.php?rid=3214789&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2010-01-28.htm</link>
            <description>Roche announced today that the European Commission has approved Herceptin (trastuzumab) in combination with chemotherapy for use in patients with HER2-positive metastatic stomach (gastric) cancer. The approval is based on the impressive results from the international ToGA trial, which showed that treatment with Herceptin significantly prolongs the lives of patients with this aggressive cancer. (Source: Roche Investor Update)</description>
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            <pubDate>Thu, 28 Jan 2010 06:00:00 +0100</pubDate>
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            <title>Reminder: Roche&amp;#039;s Full Year Results for 2009</title>
            <link>http://www.medworm.com/index.php?rid=3296774&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Finvestors%2Fir_update%2Finv-update-2010-01-27.htm</link>
            <description>Roche will publish its Full Year Results for 2009 prior to the opening of the Swiss Stock Exchange on February 3 at 7:00 CET / 6:00 GMT / 1:00 AM EST. Concurrently, the Full Year Presentation Slides and the Full Year Report will be available on te website http://ir.roche.com. We would like to invite all interested parties to dial in or participate in any of the scheduled events outlined below: 3 February; 8:00 CET &amp;#8211; Morning Telephone Conference - 3 February; 15:00 GMT - Presentation in London (16:00 CET) - 5 February; 12:30 PM EST &amp;#8211; Presentation in New York (18:30 CET) (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
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            <pubDate>Wed, 27 Jan 2010 09:00:00 +0100</pubDate>
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            <title>Roche&amp;#039;s Full Year Results for 2009</title>
            <link>http://www.medworm.com/index.php?rid=3296775&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Finvestors%2Fir_update%2Finv-update-2010-01-04.htm</link>
            <description>Roche will publish its Full Year Results for 2009 prior to the opening of the Swiss Stock Exchange on February 3 at 7:00 CET / 6:00 GMT / 1:00 AM EST. Concurrently, the Full Year Presentation Slides and the Full Year Report will be available on te website http://ir.roche.com. We would like to invite all interested parties to dial in or participate in any of the scheduled events outlined below: 3 February; 8:00 CET &amp;#8211; Morning Telephone Conference - 3 February; 15:00 GMT - Presentation in London (16:00 CET) - 5 February; 12:30 PM EST &amp;#8211; Presentation in New York (18:30 CET) (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
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            <pubDate>Mon, 04 Jan 2010 09:00:00 +0100</pubDate>
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            <title>Roche&amp;#039;s Full Year Results for 2009</title>
            <link>http://www.medworm.com/index.php?rid=3138379&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2010-01-04.htm</link>
            <description>Roche will publish its Full Year Results for 2009 prior to the opening of the Swiss Stock Exchange on February 3 at 7:00 CET / 6:00 GMT / 1:00 AM EST. Concurrently, the Full Year Presentation Slides and the Full Year Report will be available on te website http://ir.roche.com. We would like to invite all interested parties to dial in or participate in any of the scheduled events outlined below: 3 February; 8:00 CET &amp;#8211; Morning Telephone Conference - 3 February; 15:00 GMT - Presentation in London (16:00 CET) - 5 February; 12:30 PM EST &amp;#8211; Presentation in New York (18:30 CET) (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
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            <pubDate>Mon, 04 Jan 2010 09:00:00 +0100</pubDate>
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            <title>Xeloda in combination with oxaliplatin filed in Europe for the adjuvant treatment of patients with early colon cancer</title>
            <link>http://www.medworm.com/index.php?rid=3296776&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Finvestors%2Fir_update%2Finv-update-2010-01-04b.htm</link>
            <description>Roche announced today that it has submitted an application to the European Medicines Agency (EMEA) to extend the label of Xeloda (capecitabine) for use in combination with oxaliplatin (XELOX) in the adjuvant (post-surgery) treatment of patients with early colon cancer. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
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            <pubDate>Mon, 04 Jan 2010 06:00:00 +0100</pubDate>
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            <title>Genentech Submits Supplemental Application to FDA for Lucentis in Patients with Retinal Vein Occlusion</title>
            <link>http://www.medworm.com/index.php?rid=3296777&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Finvestors%2Fir_update%2Finv-update-2009-12-22.htm</link>
            <description>Genentech, Inc., a wholly owned member of the Roche Group, today announced that the company submitted a supplemental Biologics License Application (sBLA) to the U.S. Food and Drug Administration (FDA) for Lucentis (ranibizumab injection) for patients with macular edema following retinal vein occlusion (RVO). (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
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            <pubDate>Tue, 22 Dec 2009 07:45:00 +0100</pubDate>
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            <title>Investor meeting Thursday 18 March 2010 New York</title>
            <link>http://www.medworm.com/index.php?rid=3103525&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-12-18b.htm</link>
            <description>Dr Severin Schwan (CEO Roche Group) and the Roche Investor Relations team would like to invite you to the first Investor meeting since the integration of Roche and Genentech, to be held on Thursday 18 March 2010 in New York. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
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            <pubDate>Fri, 18 Dec 2009 14:42:00 +0100</pubDate>
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            <title>Herceptin receives positive opinion in record time for the treatment of HER2-positive advanced stomach cancer in Europe</title>
            <link>http://www.medworm.com/index.php?rid=3098738&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-12-18.htm</link>
            <description>Roche announced today that the European Medicines Agency (EMEA) Committee on Human Medicinal Products (CHMP) has issued a positive recommendation for the use of Herceptin (trastuzumab) in combination with standard chemotherapy for the treatment of patients with HER2-positive metastatic stomach (gastric) cancer (metastatic adenocarcinoma of the stomach or gastro-esophageal junction). (Source: Roche Investor Update)</description>
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            <pubDate>Fri, 18 Dec 2009 12:45:00 +0100</pubDate>
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            <title>Roche&amp;#039;s weekly taspoglutide meets primary end-points in two further head-to-head Phase III clinical trial comparisons with insulin glargine (Lantus) and also versus placebo in patients with high body mass index (BMI)</title>
            <link>http://www.medworm.com/index.php?rid=3094717&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-12-17b.htm</link>
            <description>Taspoglutide demonstrates non-inferiority HbA1c change versus insulin glargine and superiority in HbA1c change versus placebo (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
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            <pubDate>Thu, 17 Dec 2009 06:00:00 +0100</pubDate>
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            <title>Early-stage breast cancer study with Avastin (E5103) will resume enrolment and continue as planned</title>
            <link>http://www.medworm.com/index.php?rid=3083758&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-12-14b.htm</link>
            <description>Roche has been informed that the U.S. Food and Drug Administration (FDA) is allowing enrolment to resume into a phase III clinical trial (E5103) evaluating Avastin in combination with anthracycline, cyclophosphamide and paclitaxel chemotherapy in women with early-stage HER2-negative breast cancer. E5103 is sponspored by the National Cancer Institute (NCI) under a Cooperative Research and Development Agreement between the NCI and Genentech, a wholly-owned member of the Roche Group, and is being conducted by a network of researchers led by the Eastern Cooperative Oncology Group (ECOG). (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
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        <comments>http://www.medworm.com/rss/comments.php?id=3083758</comments>
            <pubDate>Mon, 14 Dec 2009 06:00:00 +0100</pubDate>
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        <item>
            <title>Greater chances of cure for patients with HER2-positive early breast cancer when treated with one year of Herceptin</title>
            <link>http://www.medworm.com/index.php?rid=3083757&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-12-14.htm</link>
            <description>Roche announced new long-term follow up-data from two large pivotal studies evaluating adjuvant Herceptin in HER2-positive early- stage breast cancer presented this weekend at the CTRC-AACR San Antonio Breast Cancer Symposium (SABCS). Both studies, N9831 conducted by the North Central Cancer Treatment Group (NCCTG) and BCIRG006 performed by the Breast Cancer International Research Group consistently showed that Herceptin reduced the risk of the cancer returning by about one third in women with HER2-positive early breast cancer compared to patients receiving chemotherapy alone. In both studies, at least 80% of women receiving one year of Herceptin were alive free of the disease at 5 years follow-up. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3083757</comments>
            <pubDate>Mon, 14 Dec 2009 06:00:00 +0100</pubDate>
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        <item>
            <title>New Phase II study showed trastuzumab-DM1 shrank tumours in women with highly advanced HER2-positive breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=3081424&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-12-12b.htm</link>
            <description>Roche today announced positive results from a Phase II study of trastuzumab-DM1 (T-DM1). As assessed by independent review, T-DM1 shrank the tumors (also known as objective response) in 33 percent of women with advanced (metastatic) HER2-positive breast cancer that had worsened following previous treatment. Women in the study had already received an average of seven drugs for metastatic disease, including chemotherapy, trastuzumab and lapatinib, prior to receiving T-DM1. No new or unexpected safety signals were observed. Results were presented today at the 32nd Annual San Antonio Breast Cancer Symposium (Abstract #710). (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3081424</comments>
            <pubDate>Sat, 12 Dec 2009 13:00:00 +0100</pubDate>
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        <item>
            <title>Avastin plus commonly used chemotherapies improves time without the disease getting worse in women with previously treated advanced breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=3081425&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-12-11.htm</link>
            <description>Roche today announced results from a phase III study (RIBBON 2) of Avastin&amp;#174; (bevacizumab) in women with advanced HER2-negative breast cancer who had previously received chemotherapy as first-line treatment. The study showed that women who received Avastin in combination with commonly used chemotherapies as second-line treatment had a 28% improvement in the chance of being alive without the disease getting worse (progression-free survival or PFS) compared to chemotherapy alone. Adverse events were consistent with those previously reported for Avastin and no new Avastin safety findings were observed in the study. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3081425</comments>
            <pubDate>Fri, 11 Dec 2009 18:30:00 +0100</pubDate>
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        <item>
            <title>Roche, Genentech and Biogen Idec announce positive results from first phase III trial of ocrelizumab in rheumatoid arthritis</title>
            <link>http://www.medworm.com/index.php?rid=3081426&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-12-11b.htm</link>
            <description>Roche, Genentech, Inc. a wholly owned member of the Roche Group, and Biogen Idec announced today a Phase III study (STAGE) of the investigational humanized anti-CD20 monoclonal antibody ocrelizumab given in combination with methotrexate (MTX) met its primary endpoint of improving signs and symptoms (as measured by American College of Rheumatology or ACR20 response) in rheumatoid arthritis (RA) patients who had an inadequate response to MTX at both 24 and 48 weeks. The companies continue to analyze the study results and plan to submit the data for presentation at an upcoming medical meeting. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3081426</comments>
            <pubDate>Fri, 11 Dec 2009 17:00:00 +0100</pubDate>
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        <item>
            <title>Positive interim analysis supports early closure of heart failure trial</title>
            <link>http://www.medworm.com/index.php?rid=3077726&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-12-11c.htm</link>
            <description>Further analysis could promote new paradigm in the management of heart failure. Roche and study investigators at the Massachusetts General Hospital have announced today that active enrollment into the Pro-BNP Outpatient Tailored Congestive Heart Failure Therapy (PROTECT) study (Clinical Trials.gov identifier: NCT00351390) has been stopped early based on a positive interim analysis. PROTECT, a prospective randomized trial comparing a strategy of aggressive heart failure therapy guided by levels of a cardiac hormone&amp;#8212;amino-terminal pro-B type natriuretic peptide (NT-proBNP)&amp;#8212;versus standard heart failure treatment without NT-proBNP guidance has been enrolling subjects in the Heart Center at the Massachusetts General Hospital since 2006. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3077726</comments>
            <pubDate>Fri, 11 Dec 2009 06:00:00 +0100</pubDate>
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        <item>
            <title>Roche Introduces New Automated Clinical Laboratory System for CE-Marked Testing of Human Papillomavirus, Chlamydia and N. gonorrhoeae</title>
            <link>http://www.medworm.com/index.php?rid=3073769&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-12-09b.htm</link>
            <description>Roche Molecular Systems, Inc. announced today the launch of a new clinical laboratory system designed to increase laboratory testing efficiency and to accommodate current and long-term molecular diagnostic needs. The cobas&amp;#174; 4800 System combines CE-marked in vitro diagnostic tests for Chlamydia trachomatis (CT), Neisseria gonorrhoeae (NG) and human papillomavirus (HPV) testing with fully-automated sample preparation and real-time polymerase chain reaction (PCR) technology. The tests are designed to detect the 14 HPV high-risk genotypes widely accepted to cause cervical cancer and bacterial DNA associated with chlamydia and gonorrhea infections. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3073769</comments>
            <pubDate>Wed, 09 Dec 2009 17:00:00 +0100</pubDate>
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        <item>
            <title>Important progress in treatment of early and late stage breast cancer with Herceptin, Avastin and T-DM1</title>
            <link>http://www.medworm.com/index.php?rid=3069402&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-12-09.htm</link>
            <description>Roche announced today that new 5 year follow-up data from two pivotal studies with Herceptin&amp;#174; (trastuzumab) in early breast cancer; key results from a study of Avastin&amp;#174; (bevacizumab) in the second-line treatment of advanced breast cancer and strong data on the use of trastuzumab-DM1 (T-DM1), the first antibody-drug conjugate in development for very advanced HER2-positive breast cancer, will all be presented during the CTRC-AACR San Antonio Breast Cancer Symposium (SABCS) from 9 to 13 December 2009. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3069402</comments>
            <pubDate>Wed, 09 Dec 2009 06:00:00 +0100</pubDate>
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        <item>
            <title>MabThera/Rituxan is the first treatment to show improved overall survival in previously untreated patients with chronic lymphocytic leukemia</title>
            <link>http://www.medworm.com/index.php?rid=3065471&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-12-08.htm</link>
            <description>Roche announced today at the 51st Meeting of the American Society of Hematology (ASH) in New Orleans, LA (USA) that the pivotal Phase III study CLL8 showed that patients with previously-untreated chronic lymphocytic leukemia (CLL) survived their disease longer when treated with MabThera/Rituxan (rituximab) compared to chemotherapy alone. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3065471</comments>
            <pubDate>Tue, 08 Dec 2009 06:00:00 +0100</pubDate>
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        <item>
            <title>Reminder: Invitation to Roche investor science event from SABCS 2009</title>
            <link>http://www.medworm.com/index.php?rid=3065472&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-12-07.htm</link>
            <description>We kindly invite investors and analysts to participate in a conference call to discuss new clinical data and results presented during the 32nd Annual San Antonio Breast Cancer Symposium, 9-13 December 2009, San Antonio, Texas: Monday, 14 December 2009 at 17:00 CET / 8:00am PST / 16:00 GMT (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3065472</comments>
            <pubDate>Mon, 07 Dec 2009 17:00:00 +0100</pubDate>
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        <item>
            <title>Roche reports positive phase II results with ocrelizumab in relapsing-remitting multiple sclerosis (RRMS)</title>
            <link>http://www.medworm.com/index.php?rid=3054837&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-12-04b.htm</link>
            <description>Roche and its development partner Biogen Idec have reported positive phase II data with ocrelizumab, a humanized anti-CD20 monoclonal antibody, in patients with relapsing-remitting multiple sclerosis (RRMS), one of the leading causes of neurological disability in young adults. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3054837</comments>
            <pubDate>Fri, 04 Dec 2009 06:00:00 +0100</pubDate>
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        <item>
            <title>MabThera/Rituxan: promising new data in leukemia and lymphatic cancers to be presented at the American Society of Hematology (ASH), the world&amp;#039;s leading meeting in blood cancers</title>
            <link>http://www.medworm.com/index.php?rid=3054836&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-12-04.htm</link>
            <description>Roche announced today that updated results of the pivotal phase III study, CLL8, will be one of many key presentations at the forthcoming 51st Annual Meeting of the American Society of Hematology (ASH) in New Orleans. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3054836</comments>
            <pubDate>Fri, 04 Dec 2009 06:00:00 +0100</pubDate>
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        <item>
            <title>Results from two further Phase III clinical trials show that Roche&amp;#146;s weekly taspoglutide met its primary end-points in head to head study with sitagliptin (Januvia) and versus placebo</title>
            <link>http://www.medworm.com/index.php?rid=3046726&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-12-02.htm</link>
            <description>Roche today announced headline results from the second and third of eight T-emerge Phase III studies for taspoglutide. T-emerge 1 (subcutaneous weekly taspoglutide versus placebo in treatment-na&amp;#239;ve patients) and T-emerge 4 (subcutaneous weekly taspoglutide versus sitagliptin versus placebo) both met their respective primary endpoints of change in HbA1c. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3046726</comments>
            <pubDate>Wed, 02 Dec 2009 06:00:00 +0100</pubDate>
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        <item>
            <title>Reminder: Invitation to Roche investor science event from ASH 2009 - Conference call on 8 December 2009</title>
            <link>http://www.medworm.com/index.php?rid=3042516&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-12-01.htm</link>
            <description>We kindly invite investors and analysts to participate in a conference call to discuss new clinical data and results presented during the 2009 ASH annual meeting (The 51st Annual Meeting and Exposition of the American Society of Hematology, 5-8 December 2009, New Orleans, Louisana) (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3042516</comments>
            <pubDate>Tue, 01 Dec 2009 17:00:00 +0100</pubDate>
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        <item>
            <title>Avastin filed for broader breast cancer label in Europe for use in combination with standard chemotherapies</title>
            <link>http://www.medworm.com/index.php?rid=3025057&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-11-25.htm</link>
            <description>Roche announced today that they have filed to extend the current European label of Avastin (bevacizumab) in patients with metastatic breast cancer to allow its use in combination with a broader range of standard chemotherapies. Avastin is currently licensed in the EU as first-line treatment for patients with metastatic breast cancer in combination with paclitaxel or docetaxel. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3025057</comments>
            <pubDate>Wed, 25 Nov 2009 06:00:00 +0100</pubDate>
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        <item>
            <title>European medical advisory committee does not recommend approval of Avastin for deadly form of brain cancer</title>
            <link>http://www.medworm.com/index.php?rid=3014309&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-11-20b.htm</link>
            <description>Roche announced today that the Committee for Medicinal Products for Human Use (CHMP), which is responsible for conducting the initial assessment of medicinal products that have been filed for marketing authorisation in Europe, has issued a negative opinion relating to the approval of Avastin (bevacizumab) alone or in combination with irinotecan chemotherapy for the treatment of relapsed or progressive glioblastoma (GBM), the most aggressive type of primary malignant brain cancer. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3014309</comments>
            <pubDate>Fri, 20 Nov 2009 16:45:00 +0100</pubDate>
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        <item>
            <title>ACTEMRA Improves Signs and Symptoms in Children with Systemic Onset Juvenile Idiopathic Arthritis (sJIA)</title>
            <link>http://www.medworm.com/index.php?rid=3010789&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-11-20.htm</link>
            <description>Roche announced today that ACTEMRA (tocilizumab, known as RoACTEMRA within the EU) successfully met its primary endpoint in a paediatric study of systemic onset Juvenile Idiopathic Arthritis (sJIA), by significantly improving disease signs and symptoms, a critical effectiveness measure of a sJIA treatment. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3010789</comments>
            <pubDate>Fri, 20 Nov 2009 06:00:00 +0100</pubDate>
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        <item>
            <title>US FDA issues complete response letter for Rituxan/MabThera for chronic lymphocytic leukaemia</title>
            <link>http://www.medworm.com/index.php?rid=3006421&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-11-18.htm</link>
            <description>Roche announced today that the US Food and Drug Administration (FDA) issued a complete response to Genentech, a wholly-owned member of the Roche Group, and Biogen Idec (Nasdaq: BIIB) on the companies&amp;#8217; applications for Rituxan/MabThera (rituximab) plus fludarabine and cyclophosphamide (FC) chemotherapy for the treatment of for the treatment of patients with previously untreated and previously treated chronic lymphocytic leukaemia (CLL). (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3006421</comments>
            <pubDate>Wed, 18 Nov 2009 21:02:00 +0100</pubDate>
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        <item>
            <title>Invitation to Roche investor science event from SABCS 2009</title>
            <link>http://www.medworm.com/index.php?rid=3002241&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-11-18c.htm</link>
            <description>We kindly invite investors and analysts to participate in a conference call to discuss new clinical data and results presented during the 32nd Annual San Antonio Breast Cancer Symposium, 9-13 December 2009, San Antonio, Texas. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3002241</comments>
            <pubDate>Wed, 18 Nov 2009 13:00:00 +0100</pubDate>
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        <item>
            <title>Roche announces start of new atherosclerosis study (dal-PLAQUE 2) for dalcetrapib</title>
            <link>http://www.medworm.com/index.php?rid=3002242&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-11-18b.htm</link>
            <description>Roche today presented new preclinical data further supporting the differentiation of its novel cholesteryl ester transfer protein inhibitor (CETPi) dalcetrapib at this year&amp;#039;s Scientific Sessions of the American Heart Association taking place from 14-18 November in Orlando. Based on the current safety and efficacy profile of dalcetrapib, Roche announced a new Phase III clinical trial, dal-PLAQUE 2. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3002242</comments>
            <pubDate>Wed, 18 Nov 2009 06:00:00 +0100</pubDate>
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            <title>Applications to allow Avastin to be combined with commonly used chemotherapies in advanced breast cancer submitted to FDA</title>
            <link>http://www.medworm.com/index.php?rid=2998019&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-11-17.htm</link>
            <description>Roche announced today that Genentech, a wholly-owned member of the Roche Group, has submitted two supplemental Biologics License Applications (sBLAs) to the U.S. Food and Drug Administration (FDA) for Avastin&amp;#174; (bevacizumab) for the treatment of women who have not received chemotherapy for advanced (metastatic) HER2-negative breast cancer (first-line treatment). One sBLA is based on the phase III AVADO study that investigated Avastin in combination with docetaxel chemotherapy. The other is based on the phase III RIBBON-1 study that investigated Avastin in combination with a taxane or anthracycline-based chemotherapy or the oral chemotherapy, Xeloda (capecitabine). (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2998019</comments>
            <pubDate>Tue, 17 Nov 2009 06:00:00 +0100</pubDate>
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        <item>
            <title>FDA Grants Emergency Use Authorization to Roche&amp;#039;s Assay for 2009 H1N1 Influenza Virus</title>
            <link>http://www.medworm.com/index.php?rid=2998020&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-11-16.htm</link>
            <description>Roche announced today that it&amp;#039;s RealTime ready Influenza A/H1N1 Detection Set for the 2009 H1N1 influenza virus has received emergency use authorization (EUA) from the U.S. Food and Drug Administration (FDA). The Roche kit detects RNA from the 2009 H1N1 influenza A virus and allows rapid and accurate identification of patients infected with this virus. It is important to differentiate patients infected with 2009 H1N1 virus from others with similar symptoms so that appropriate patient management can be commenced as early as possible. The efficacy of the Roche assay was demonstrated by clinical evaluation at worldwide study sites. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2998020</comments>
            <pubDate>Mon, 16 Nov 2009 17:00:00 +0100</pubDate>
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        <item>
            <title>Roche reports positive Phase II results with potential first-in-class treatment for the negative symptoms of schizophrenia</title>
            <link>http://www.medworm.com/index.php?rid=2975932&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-11-10.htm</link>
            <description>Roche today reports results from a 320 patient phase II proof-of-concept study with it&amp;#8217;s investigational glycine transporter-1 inhibitor RG1678. The study showed that the compound improved both the negative symptoms and the personal and social functioning of patients with schizophrenia reaching statistical significance on primary and secondary endpoints. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2975932</comments>
            <pubDate>Tue, 10 Nov 2009 06:00:00 +0100</pubDate>
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        <item>
            <title>Invitation to Roche investor science event from ASH 2009 - Conference call on 8 December 2009</title>
            <link>http://www.medworm.com/index.php?rid=2972849&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-11-09b.htm</link>
            <description>(Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2972849</comments>
            <pubDate>Mon, 09 Nov 2009 09:00:00 +0100</pubDate>
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        <item>
            <title>Anti-Malignancy Agent Avastin Obtained Approval for Additional Indication of Non-Small Cell Lung Cancer</title>
            <link>http://www.medworm.com/index.php?rid=2972850&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-11-09.htm</link>
            <description>Please find attached a press release issued by Chugai in Japan (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2972850</comments>
            <pubDate>Mon, 09 Nov 2009 06:00:00 +0100</pubDate>
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        <item>
            <title>First Phase III clinical trial of  Roche`s weekly taspoglutide meets primary end-point of change in HbA1c</title>
            <link>http://www.medworm.com/index.php?rid=2953089&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-10-29.htm</link>
            <description>Roche today announced that headline results from its Phase III study, T-emerge 2 (subcutaneous weekly taspoglutide versus subcutaneous twice-daily exenatide, as add-on to metformin, a thiazolidinedione [TZD], or metformin and a TZD), showed that the trial met its primary endpoint of change in HbA1c. Superiority versus exenatide was demonstrated. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2953089</comments>
            <pubDate>Thu, 29 Oct 2009 06:00:00 +0100</pubDate>
            <guid isPermaLink="false">2953089</guid>        </item>
        <item>
            <title>First Phase III clinical trial of  Roche&amp;#039;s weekly taspoglutide meets primary end-point of change in HbA1c</title>
            <link>http://www.medworm.com/index.php?rid=2937090&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-10-29.htm</link>
            <description>Roche today announced that headline results from its Phase III study, T-emerge 2 (subcutaneous weekly taspoglutide versus subcutaneous twice-daily exenatide, as add-on to metformin, a thiazolidinedione [TZD], or metformin and a TZD), showed that the trial met its primary endpoint of change in HbA1c. Superiority versus exenatide was demonstrated. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2937090</comments>
            <pubDate>Thu, 29 Oct 2009 06:00:00 +0100</pubDate>
            <guid isPermaLink="false">2937090</guid>        </item>
        <item>
            <title>Phase III trial underway to investigate infusion-free administration of Herceptin for women with HER2-positive breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=2914461&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-10-22.htm</link>
            <description>Roche and Halozyme Therapeutics announced today that a new subcutaneous formulation of Herceptin using Halozyme&amp;#8217;s Enhanze technology has entered phase III of its development. This innovative technology could allow patients with HER2-positive breast cancer to administer Herceptin for themselves with or without the support of a healthcare professional once every three weeks via a simple subcutaneous injection. Currently Herceptin, which prolongs lives of patients with this aggressive type of breast cancer, is given intravenously typically in a hospital setting at the same frequency. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2914461</comments>
            <pubDate>Thu, 22 Oct 2009 05:00:00 +0100</pubDate>
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        <item>
            <title>Genentech and Biogen Idec Receive a Complete Response from FDA for Earlier Use of Rituxan for Rheumatoid Arthritis</title>
            <link>http://www.medworm.com/index.php?rid=2903944&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-10-19.htm</link>
            <description>Please find attached a press release issued by Genentech and Biogen Idec in the US with respect to the approval of Rituxan in early and late stage rheumatoid arthritis in the US. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2903944</comments>
            <pubDate>Mon, 19 Oct 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2903944</guid>        </item>
        <item>
            <title>Anti-Malignancy Agent/Anti-VEGF Humanized Monoclonal Antibody, Avastin Application for Approval of Additional Indication of Breast Cancer</title>
            <link>http://www.medworm.com/index.php?rid=2897153&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-10-16.htm</link>
            <description>Please find enclosed a press release by Chugai (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2897153</comments>
            <pubDate>Fri, 16 Oct 2009 02:00:00 +0100</pubDate>
            <guid isPermaLink="false">2897153</guid>        </item>
        <item>
            <title>Roche reports further accelerated sales growth in third quarter</title>
            <link>http://www.medworm.com/index.php?rid=2892829&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-10-15.htm</link>
            <description>Group sales up 3.1 billion to 36.4 billion Swiss francs in first nine months, an increase of 11% in local currencies (9% in Swiss francs); both divisions grow significantly faster than their respective markets; Genentech integration progressing successfully; New Group leadership appointed (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2892829</comments>
            <pubDate>Thu, 15 Oct 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2892829</guid>        </item>
        <item>
            <title>Reminder: Roche&amp;#039;s Third Quarter Sales 2009 Conference Call</title>
            <link>http://www.medworm.com/index.php?rid=2867718&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-10-07.htm</link>
            <description>Roche will publish its Sales Results for the 3rd Quarter of 2009 prior to the opening of the Swiss Stock Exchange on Thursday 15th October, 2009. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2867718</comments>
            <pubDate>Wed, 07 Oct 2009 08:00:00 +0100</pubDate>
            <guid isPermaLink="false">2867718</guid>        </item>
        <item>
            <title>Two Phase III studies of Lucentis show early and sustained improvement in vision in patients with retinal vein occlusion</title>
            <link>http://www.medworm.com/index.php?rid=2860784&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-10-05.htm</link>
            <description>Genentech, Inc., a wholly-owned member of the Roche Group yesterday announced results from two Phase III studies of Lucentis&amp;#174; (ranibizumab injection) in macular edema due to retinal vein occlusion (RVO), which showed, on average, patients given either of two doses of Lucentis had a clinically and statistically significant improvement in vision as measured by the primary endpoint of mean change from baseline in best-corrected visual acuity (BCVA) at six months compared to patients receiving sham injections. Results from both trials were presented today at the Retina Congress 2009 meeting. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2860784</comments>
            <pubDate>Mon, 05 Oct 2009 05:00:00 +0100</pubDate>
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        <item>
            <title>RoACTEMRA filed in Europe for the Inhibition of Joint Damage and Improvement in Physical Function in Rheumatoid Arthritis</title>
            <link>http://www.medworm.com/index.php?rid=2844796&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-09-30.htm</link>
            <description>Roche announced today that it has submitted a filing to the European health authorities (the European Medicines Agency) to extend the indication of RoACTEMRA to inhibit the progression of joint damage and to improve physical function in patients with rheumatoid arthritis (RA). Joint damage in RA often begins early in the disease and can lead to permanent disability, so inhibiting this structural damage to patients&amp;#039; joints is a critical measure of effectiveness of an RA treatment. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2844796</comments>
            <pubDate>Wed, 30 Sep 2009 05:00:00 +0100</pubDate>
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        <item>
            <title>Roche provides update on early-stage breast cancer study with Avastin</title>
            <link>http://www.medworm.com/index.php?rid=2837773&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-09-25.htm</link>
            <description>Roche has been informed by the National Cancer Institute and US Eastern Cooperative Oncology Group (ECOG) that they have suspended enrollment into a phase III clinical trial (E5103) evaluating Avastin&amp;#174; (bevacizumab) in combination with chemotherapy in women with early-stage breast cancer based on a pre-planned cardio-toxicity analysis of the first 200 patients enrolled. The protocol for the trial specifies that enrollment be suspended if six or more cases of clinical congestive heart failure (CHF) are seen in the first 200 patients. This threshold has been met. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2837773</comments>
            <pubDate>Fri, 25 Sep 2009 17:00:00 +0100</pubDate>
            <guid isPermaLink="false">2837773</guid>        </item>
        <item>
            <title>Herceptin provides impressive survival benefit for patients with high levels of HER2 in their stomach cancer</title>
            <link>http://www.medworm.com/index.php?rid=2826780&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-09-24c.htm</link>
            <description>A detailed analysis of the Phase III ToGA study announced today revealed an unprecedented survival benefit for patients whose tumours exhibited a particularly high level of HER2 when Herceptin (trastuzumab) was added to standard chemotherapy (Xeloda or intravenous 5-FU and cisplatin). (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2826780</comments>
            <pubDate>Thu, 24 Sep 2009 11:10:00 +0100</pubDate>
            <guid isPermaLink="false">2826780</guid>        </item>
        <item>
            <title>Continuous improvements in animal welfare within Roche Research</title>
            <link>http://www.medworm.com/index.php?rid=2826781&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-09-24b.htm</link>
            <description>Roche announced the winners of its global 3Rs Award Program - a unique and innovative program that helps to reduce and limit the use of animals in preclinical research - to recognise and reward innovation and continuous improvement in animal welfare within the Roche research organisation. The award, which is now in its second year, is based on the 3Rs concept, which means Replacing animal tests where possible, Reducing the number of animals required and Refining existing scientific practices as well as animal care and husbandry. Fifteen teams of Roche scientists and animal care specialists from the companies&amp;#8217; global research sites in Basel, Penzberg, Nutley and Tokyo applied for awards in two categories: &amp;#8220;Scientific Progress Fostering the 3Rs Idea&amp;#8221; and &amp;#8220;Laboratory A...</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2826781</comments>
            <pubDate>Thu, 24 Sep 2009 07:00:00 +0100</pubDate>
            <guid isPermaLink="false">2826781</guid>        </item>
        <item>
            <title>Anti-Cancer Agent Xeloda and Avastin Obtained Approval for Additional Indication of Colorectal Cancer</title>
            <link>http://www.medworm.com/index.php?rid=2826782&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-09-24.htm</link>
            <description>Please find enclosed a press release by Chugai (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2826782</comments>
            <pubDate>Thu, 24 Sep 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2826782</guid>        </item>
        <item>
            <title>Adding Xeloda to standard chemotherapy before surgery helps to eradicate tumours in patients with early breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=2822614&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-09-23d.htm</link>
            <description>Results from the ABCSG 24 trial presented today at the joint 15th ECCO and 34th ESMO 2009 congress, Berlin, Germany showed that the addition of Xeloda (capecitabine) to anthracycline- and taxane-containing regimens prior to surgery (neoadjuvant therapy) led to complete eradication of the tumour in 24% of women with HER2-positive or HER2-negative early breast cancer. The increased efficacy seen obtained by adding Xeloda was measured by an increase in the pathological complete response (pCR) rate from 16% to 24% (hazard ratio of 0.58, p=0.02). This is an important finding since the proportion of women whose tumour completely disappears when treated with standard chemotherapy for HER2-positive or HER2-negative early breast cancer is typically less than 20% (range 6&amp;#8211;18%). (Source: Roche ...</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2822614</comments>
            <pubDate>Wed, 23 Sep 2009 12:05:00 +0100</pubDate>
            <guid isPermaLink="false">2822614</guid>        </item>
        <item>
            <title>From inoperable disease to potentially life saving surgery - new Avastin data gives hope to colorectal cancer patients with liver metastases</title>
            <link>http://www.medworm.com/index.php?rid=2822615&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-09-23c.htm</link>
            <description>New data from several studies presented at ECCO 151 and ESMO 342 confirm unique benefits of Avastin (bevacizumab) and Xeloda (capecitabine) in treatment of colon cancer (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2822615</comments>
            <pubDate>Wed, 23 Sep 2009 12:00:00 +0100</pubDate>
            <guid isPermaLink="false">2822615</guid>        </item>
        <item>
            <title>Roche announces results from two early studies which show promise for patients with malignant melanoma</title>
            <link>http://www.medworm.com/index.php?rid=2822616&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-09-23b.htm</link>
            <description>New data from phase II Avastin study and a phase I extension study of highly selective BRAF inhibitor (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2822616</comments>
            <pubDate>Wed, 23 Sep 2009 09:15:00 +0100</pubDate>
            <guid isPermaLink="false">2822616</guid>        </item>
        <item>
            <title>Phase IV lung cancer study confirms the safety and outstanding efficacy benefit of Avastin-based therapy in a &amp;#039;real world&amp;#039; setting.</title>
            <link>http://www.medworm.com/index.php?rid=2822617&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-09-23a.htm</link>
            <description>Key data from four presentations at the joint ECCO 15 and ESMO 34 congress strongly support the clinical benefit of Avastin in advanced non-small cell lung cancer (NSCLC) (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2822617</comments>
            <pubDate>Wed, 23 Sep 2009 07:00:00 +0100</pubDate>
            <guid isPermaLink="false">2822617</guid>        </item>
        <item>
            <title>Reminder: Roche Investor Science Event: Conference Call from ECCO ESMO 2009 - Friday, September 25th, 2009</title>
            <link>http://www.medworm.com/index.php?rid=2813675&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-09-21b.htm</link>
            <description>We are pleased to invite you to a Conference Call to discuss new data on Roche&amp;#8217;s oncology products and pipeline being presented during the joint 15th Congress of the European Cancer Organisation (ECCO) and 34th Congress of the European Society for Medical Oncology (ESMO), which runs from September 20th &amp;#8211; September 24th, 2009 in Berlin, Germany. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2813675</comments>
            <pubDate>Mon, 21 Sep 2009 08:00:00 +0100</pubDate>
            <guid isPermaLink="false">2813675</guid>        </item>
        <item>
            <title>Roche to present new survival data from phase II, III and IV studies for Avastin, Herceptin and Xeloda</title>
            <link>http://www.medworm.com/index.php?rid=2813676&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-09-21.htm</link>
            <description>Nearly 150 abstracts covering new tumour types, new patient groups and existing indications to feature in ECCO-ESMO program
Roche will present encouraging results from nearly 150 scientific studies investigating use of its major cancer medicines at ECCO 15 ESMO 34, which opens in Berlin, Germany today. Overall survival benefits will be demonstrated for Avastin (bevacizumab) in malignant melanoma and for Herceptin (trastuzumab) in gastric cancer. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2813676</comments>
            <pubDate>Mon, 21 Sep 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2813676</guid>        </item>
        <item>
            <title>Antineoplastic Agent / Epidermal Growth Factor Receptor (EGFR) Tyrosine Kinase Inhibitor, Tarceva</title>
            <link>http://www.medworm.com/index.php?rid=2806228&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-09-18.htm</link>
            <description>Application for Approval of Additional Indication of Pancreatic Cancer (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2806228</comments>
            <pubDate>Fri, 18 Sep 2009 08:05:00 +0100</pubDate>
            <guid isPermaLink="false">2806228</guid>        </item>
        <item>
            <title>Study shows MabThera maintenance treatment delays disease progression in patients with incurable lymphoma</title>
            <link>http://www.medworm.com/index.php?rid=2802675&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-09-17.htm</link>
            <description>Results show patients treated with MabThera as initial and follow-on therapy stay in remission for longer. Roche announced today results from the international phase III study PRIMA1, which show that MabThera (rituximab) maintenance therapy can significantly increase the time until the disease progresses in newly-treated patients with advanced follicular lymphoma, a common and slow-developing but incurable form of lymphoma. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2802675</comments>
            <pubDate>Thu, 17 Sep 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2802675</guid>        </item>
        <item>
            <title>Roche&amp;#039;s Third Quarter Sales 2009 Conference Call</title>
            <link>http://www.medworm.com/index.php?rid=2792124&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-09-14.htm</link>
            <description>Roche will publish its Sales Results for the 3rd Quarter of 2009 prior to the opening of the Swiss Stock Exchange on Thursday 15th October, 2009. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2792124</comments>
            <pubDate>Mon, 14 Sep 2009 12:00:00 +0100</pubDate>
            <guid isPermaLink="false">2792124</guid>        </item>
        <item>
            <title>Roche Investor Science Event: Conference Call from ECCO ESMO 2009 - Friday, September 25th, 2009</title>
            <link>http://www.medworm.com/index.php?rid=2784365&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-09-11.htm</link>
            <description>We are pleased to invite you to a Conference Call to discuss new data on Roche&amp;#8217;s oncology products and pipeline being presented during the joint 15th Congress of the European Cancer Organisation (ECCO) and 34th Congress of the European Society for Medical Oncology (ESMO), which runs from September 20th &amp;#8211; September 24th, 2009 in Berlin, Germany. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2784365</comments>
            <pubDate>Fri, 11 Sep 2009 08:00:00 +0100</pubDate>
            <guid isPermaLink="false">2784365</guid>        </item>
        <item>
            <title>Roche announces new Corporate Executive Committee</title>
            <link>http://www.medworm.com/index.php?rid=2773762&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-09-08.htm</link>
            <description>William M. Burns, Juergen Schwiezer and Jonathan Knowles to retire &amp;#8211; Pascal Soriot appointed COO Pharma Division and Daniel O&amp;#8217;Day appointed COO Diagnostics Division &amp;#8211; Jean-Jacques Garaud and Dan Zabrowski to become Members of Enlarged Executive Committee &amp;#8211; Ian Clark appointed CEO Genentech (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2773762</comments>
            <pubDate>Tue, 08 Sep 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2773762</guid>        </item>
        <item>
            <title>Roche recognised as new Super Sector Leader in Dow Jones Sustainability Index</title>
            <link>http://www.medworm.com/index.php?rid=2760521&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-09-03b.htm</link>
            <description>Roche (SIX: RO, ROG; OTCQX: RHHBY) has been rated as the new Super Sector Leader in Healthcare on the Dow Jones Sustainability Index, placing Roche as the most sustainable healthcare company worldwide. Selection into the global Dow Jones Sustainability World Index as well as the pan-European Dow Jones STOXX Sustainability Index follows a thorough analysis of corporate economic, environmental and social performance, and takes into account elements such as corporate governance, risk management, access to medicines, climate change, supply chain standards, stakeholder engagement and labor practice. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2760521</comments>
            <pubDate>Thu, 03 Sep 2009 09:00:00 +0100</pubDate>
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        <item>
            <title>Roche receives CE Mark certification for cobas 8000 modular analyzer series</title>
            <link>http://www.medworm.com/index.php?rid=2750282&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Fcobas701_200px.jpg</link>
            <description>Roche announced today that the CE Mark certification for cobas 8000 modular analyzer series has been granted allowing commercial distribution of the first analyzers in Europe as well as in all countries recognizing the CE Mark in the EMEA, Latin America and Asia-Pacific regions. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2750282</comments>
            <pubDate>Tue, 01 Sep 2009 05:00:00 +0100</pubDate>
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        <item>
            <title>FDA Approves Valcyte (valganciclovir hydrochloride) to Prevent Cytomegalovirus (CMV) Disease in Pediatric Patients Who Receive Heart or Kidney Transplants</title>
            <link>http://www.medworm.com/index.php?rid=2746945&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-08-31b.htm</link>
            <description>Plus new oral solution offers dosing flexibility for pediatric patients. Roche announced today that the U.S. Food and Drug Administration (FDA) has approved Valcyte (valganciclovir hydrochloride) for the prevention of cytomegalovirus (CMV) disease in pediatric kidney and heart transplant patients (4 months to 16 years of age) at high risk of developing CMV disease. The FDA also approved a new pediatric oral solution formulation for Valcyte, which will allow easier administration to pediatric patients 4 months to 16 years of age. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2746945</comments>
            <pubDate>Mon, 31 Aug 2009 05:01:00 +0100</pubDate>
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        <item>
            <title>Roche and Lonza Announce Opt-in for Singapore Manufacturing Facility</title>
            <link>http://www.medworm.com/index.php?rid=2746946&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-08-31.htm</link>
            <description>Roche and Lonza announced today that Genentech Singapore Pte. Ltd. (&amp;#8220;Genentech Singapore&amp;#8221;), a wholly-owned member of the Roche Group, elected to exercise an option to purchase from Lonza its cell culture biologic manufacturing facility in Singapore. The facility, which is mechanically complete, will be merged with Genentech Singapore&amp;#039;s existing biologic manufacturing facility. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2746946</comments>
            <pubDate>Mon, 31 Aug 2009 05:00:00 +0100</pubDate>
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        <item>
            <title>Avastin plus commonly used chemotherapies improves time without the disease getting worse in women with previously treated advanced breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=2707199&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Fmed-cor-50336_avastin_200px.jpg</link>
            <description>Roche (SIX: RO, ROG; OTCQX: RHHBY) announced today that a Phase III study of Avastin (bevacizumab) in combination with a range of chemotherapies met its primary endpoint of increasing the time women with previously treated advanced HER2 negative breast cancer lived without the disease getting worse (progression-free survival or PFS) compared to chemotherapy alone. In the RIBBON-2 study, investigators chose the type of chemotherapy used in combination with Avastin and the chemotherapies were assessed together in the primary endpoint analysis. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2707199</comments>
            <pubDate>Tue, 18 Aug 2009 05:00:00 +0100</pubDate>
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        <item>
            <title>Roche Continents takes place for the third time</title>
            <link>http://www.medworm.com/index.php?rid=2669503&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Fmed-rochecontinents-200px.gif</link>
            <description>For the third time, Roche and the Salzburg Festival have invited 100 students to take part in &amp;#034;Roche Continents&amp;#034;. Students of science, music and the fine arts from 21 European countries will be spending a week together in Salzburg discussing the topic of creativity in their fields of study and uncovering the common ground in what at first glance seem to be very different disciplines. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2669503</comments>
            <pubDate>Wed, 05 Aug 2009 08:00:00 +0100</pubDate>
            <guid isPermaLink="false">2669503</guid>        </item>
        <item>
            <title>Avastin approved in US for the most common type of kidney cancer</title>
            <link>http://www.medworm.com/index.php?rid=2663500&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-08-03.htm</link>
            <description>Roche today announced that the U.S. Food and Drug Administration (FDA) has approved Avastin (bevacizumab) plus interferon alpha for people with metastatic renal cell carcinoma, the most common type of kidney cancer. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2663500</comments>
            <pubDate>Mon, 03 Aug 2009 05:00:00 +0100</pubDate>
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        <item>
            <title>Phase III study showed Tarceva helped patients with advanced non-small cell lung cancer live longer when used immediately after initial chemotherapy</title>
            <link>http://www.medworm.com/index.php?rid=2659574&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-08-01.htm</link>
            <description>Roche today announced that patients with advanced non-small cell lung cancer (NSCLC) who received Tarceva (erlotinib) immediately after initial chemotherapy in SATURN, a pivotal Phase III study, had a significant, 23% improvement in overall survival (hazard ratio =0.81; p-value=0.0088) compared to patients who received placebo. As previously announced, the safety results in this study were consistent with what has been seen before and there were no new or unexpected safety signals. Overall survival was a key secondary endpoint of the study and these new survival data were presented during the ongoing 13th World Conference on Lung Cancer being held in San Francisco. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2659574</comments>
            <pubDate>Sat, 01 Aug 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2659574</guid>        </item>
        <item>
            <title>FDA accepts complete response resubmission for ACTEMRA (tocilizumab)</title>
            <link>http://www.medworm.com/index.php?rid=2655733&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-07-31.htm</link>
            <description>Roche announced today that the U.S. Food &amp;#038; Drug Administration (FDA) has accepted the resubmission for the ACTEMRA (tocilizumab) Biologics License Application (BLA), following the company&amp;#8217;s receipt of a complete response in September 2008. The FDA has designated a Class II, or six-month, review timeline for the resubmission, according to Prescription Drug User Fee Act (PDUFA) guidelines. ACTEMRA is the first interleukin-6 (IL-6) receptor-inhibiting monoclonal antibody for the treatment of adult patients with moderately to severely active rheumatoid arthritis (RA). (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2655733</comments>
            <pubDate>Fri, 31 Jul 2009 06:00:00 +0100</pubDate>
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        <item>
            <title>Second Phase III Study Showed Lucentis Improved Vision in Patients with Retinal Vein Occlusion</title>
            <link>http://www.medworm.com/index.php?rid=2655734&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-07-30.htm</link>
            <description>Roche announced today that the Phase III study CRUISE showed Lucentis (ranibizumab injection) improved vision in patients with swelling in the retina (macular edema) due to central retinal vein occlusion (RVO). (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2655734</comments>
            <pubDate>Thu, 30 Jul 2009 16:00:00 +0100</pubDate>
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        <item>
            <title>European commission approves broader label for Avastin allowing combination with docetaxel for the first-line treatment of advanced (metastatic) breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=2647552&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-07-29.htm</link>
            <description>More patients with advanced breast cancer could benefit from Avastin as a result of a broader label allowing Avastin to be combined with both docetaxel or paclitaxel chemotherapy, Roche announced today. In March 2007, Avastin was approved in Europe for the first-line treatment of patients with advanced breast cancer, in combination with paclitaxel. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2647552</comments>
            <pubDate>Wed, 29 Jul 2009 05:00:00 +0100</pubDate>
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        <item>
            <title>Genentech Announces Appointment of Sandra J. Horning, M.D., to Senior Vice President, Global Head, Clinical Development Hematology/Oncology</title>
            <link>http://www.medworm.com/index.php?rid=2647553&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-07-28c.htm</link>
            <description>Genentech, Inc., a wholly-owned member of the Roche Group (SIX: RO, ROG; OTCQX: RHHBY), today announced the appointment of Sandra J. Horning, M.D., to senior vice president, global head, Clinical Development Hematology/Oncology. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2647553</comments>
            <pubDate>Tue, 28 Jul 2009 16:15:00 +0100</pubDate>
            <guid isPermaLink="false">2647553</guid>        </item>
        <item>
            <title>Roche and Google.org Start Initiative for Early Discovery of New Diseases</title>
            <link>http://www.medworm.com/index.php?rid=2647554&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-07-28b.htm</link>
            <description>Roche Applied Science and Google.org recently started a joint project to demonstrate the feasibility of developing a multidisciplinary surveillance, research and response system. This system will enhance the ability to predict and prevent emerging infectious diseases in East Africa. Roche has donated a Genome Sequencer FLX system as backbone of this project.&amp;#8220;We are proud to work with Google.org, and the dedicated research organizations in Kenya to bring this technology to a region of the world where novel viruses frequently emerge. We are confident that access to the 454 Sequencing Systems will improve monitoring of novel infectious diseases and enable faster discovery in case of an outbreak,&amp;#8221; said Chris McLeod, CEO of 454 Life Sciences, a member of the Roche Group. (Source: Ro...</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2647554</comments>
            <pubDate>Tue, 28 Jul 2009 12:00:00 +0100</pubDate>
            <guid isPermaLink="false">2647554</guid>        </item>
        <item>
            <title>MabThera receives positive opinion in Europe for treating patients whose chronic lymphocytic leukaemia returns</title>
            <link>http://www.medworm.com/index.php?rid=2636668&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Fmed-actemra43-200px.jpg</link>
            <description>Roche announced today that the European Union&amp;#8217;s Committee on Human Medicinal Products (CHMP) has issued a positive recommendation for the use of MabThera (rituximab) in patients with relapsed or refractory chronic lymphocytic leukaemia (CLL). Physicians will soon be able to prescribe MabThera, the first monoclonal antibody therapy approved for previously untreated CLL, in combination with chemotherapy to patients who have been treated for the disease but whose cancer has returned or have not appropriately responded to therapy. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2636668</comments>
            <pubDate>Fri, 24 Jul 2009 09:30:00 +0100</pubDate>
            <guid isPermaLink="false">2636668</guid>        </item>
        <item>
            <title>Full reconciliation of Chugai interim results into IFRS</title>
            <link>http://www.medworm.com/index.php?rid=2632692&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-07-24.htm</link>
            <description>Following the publication of Chugai&amp;#8217;s official 2009 interim results, Roche offers this investor update which reconciles these results with the results for Chugai published by Roche as part of the Roche Group&amp;#8217;s 2009 interim results. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2632692</comments>
            <pubDate>Fri, 24 Jul 2009 06:00:00 +0100</pubDate>
            <guid isPermaLink="false">2632692</guid>        </item>
        <item>
            <title>Double-digit increase in sales, operating profit and Core EPS</title>
            <link>http://www.medworm.com/index.php?rid=2628575&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-07-23.htm</link>
            <description>Integration of Genentech progressing rapidly; full-year outlook raised; Group sales up 2 billion to 24 billion Swiss francs, an increase of 10% in local currencies (9% in Swiss francs); both divisions grow significantly faster than their respective markets. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2628575</comments>
            <pubDate>Thu, 23 Jul 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2628575</guid>        </item>
        <item>
            <title>Reminder: Roche&amp;#039;s Half Year Results for 2009</title>
            <link>http://www.medworm.com/index.php?rid=2624100&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-07-22.htm</link>
            <description>Roche will publish its Half Year Results for 2009 prior to the opening of the Swiss Stock Exchange on July 23 at 7.00 CET / 6.00 GMT / 1.00 AM EDT / 22.00 PM PDT (evening before). Concurrently, the Half Year Presentation Slides and the Half Year Report will be available on the Roche website (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2624100</comments>
            <pubDate>Wed, 22 Jul 2009 08:00:00 +0100</pubDate>
            <guid isPermaLink="false">2624100</guid>        </item>
        <item>
            <title>Chugai Files NDA for a Renal Anemia Agent R744</title>
            <link>http://www.medworm.com/index.php?rid=2624101&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-07-22b.htm</link>
            <description>Please find enclosed a press release by Chugai. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2624101</comments>
            <pubDate>Wed, 22 Jul 2009 06:05:00 +0100</pubDate>
            <guid isPermaLink="false">2624101</guid>        </item>
        <item>
            <title>Roche Diagnostics showcases new technology at Clinical Lab Expo</title>
            <link>http://www.medworm.com/index.php?rid=2624102&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-07-21.htm</link>
            <description>Roche Diagnostics is featuring a diverse portfolio of solutions designed to help healthcare facilities and reference labs do more with less and enhance patient care in booth #1331 at the AACC/CSCC 2009 Clinical Lab Expo here, July 21-23. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2624102</comments>
            <pubDate>Tue, 21 Jul 2009 13:00:00 +0100</pubDate>
            <guid isPermaLink="false">2624102</guid>        </item>
        <item>
            <title>Xeloda in combination with oxaliplatin shown to be effective in early colon cancer</title>
            <link>http://www.medworm.com/index.php?rid=2616269&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-07-20.htm</link>
            <description>Roche announced today results from the international phase III study NO16968 (XELOXA), investigating oral Xeloda in combination with intravenous oxaliplatin (XELOX) immediately after surgery, which show that patients with colon cancer taking XELOX live disease free for longer compared to those taking the commonly used intravenous chemotherapy combination 5-fluorouracil/leucovorin (5-FU/LV). The data prove that XELOX is superior to 5-FU/LV in terms of the time patients live without their cancer being detectable. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2616269</comments>
            <pubDate>Mon, 20 Jul 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2616269</guid>        </item>
        <item>
            <title>New data from phase III SATURN study shows Tarceva improves overall survival when used immediately after initial chemotherapy in patients with advanced lung cancer</title>
            <link>http://www.medworm.com/index.php?rid=2593991&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-07-13.htm</link>
            <description>Roche announced today that SATURN, a pivotal Phase III study, met a key secondary endpoint of extending overall survival in patients with advanced non-small cell lung cancer (NSCLC) who received Tarceva&amp;#174; (erlotinib) immediately after their initial chemotherapy. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2593991</comments>
            <pubDate>Mon, 13 Jul 2009 05:00:00 +0100</pubDate>
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        <item>
            <title>Phase III Study Showed Lucentis Improved Vision in Patients with Branch Retinal Vein Occlusion</title>
            <link>http://www.medworm.com/index.php?rid=2566743&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-07-02.htm</link>
            <description>Roche announced today that the Phase III study BRAVO showed Lucentis (ranibizumab injection) improved vision, as measured by the primary endpoint of mean change from baseline in best-corrected visual acuity at six months, in patients with macular edema due to branch retinal vein occlusion. The safety profile of Lucentis was consistent with previous experience and no new adverse events related to Lucentis were observed in the study. Retinal vein occlusion (RVO) is a common cause of vision loss that occurs when blood flow through a retinal vein becomes blocked, such as by a blood clot. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2566743</comments>
            <pubDate>Thu, 02 Jul 2009 16:00:00 +0100</pubDate>
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        <item>
            <title>Roche launches novel program to ease Tamiflu access to developing economies</title>
            <link>http://www.medworm.com/index.php?rid=2558607&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Fmed-tamiflu-34345_200px.jpg</link>
            <description>Roche today announced the initiation of the Tamiflu Reserves Program (TRP) for developing economies. The program, which is effective immediately, will serve to ensure that Tamiflu (oseltamivir) is available to many governments and patients in developing nations for use when the World Health Organization (WHO) has declared an influenza pandemic, or for the management of a novel influenza strain defined by WHO that has significant and current pandemic potential. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2558607</comments>
            <pubDate>Wed, 01 Jul 2009 05:00:00 +0100</pubDate>
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        <item>
            <title>European regulator gives positive opinion for the use of Avastin in combination with docetaxel for the first-line treatment of advanced breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=2519613&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-06-26b.htm</link>
            <description>Physicians will be able to offer patients more Avastin-based treatment options. Patients with advanced (metastatic) breast cancer will be able to benefit from treatment with Avastin (bevacizumab) as a result of a new broader label recommendation in Europe, Roche announced today. The positive opinion issued by the European Committee for Medicinal Products for Human Use (CHMP) is for the use of Avastin in combination with paclitaxel or docetaxel chemotherapy for the first-line treatment of patients with metastatic breast cancer. Avastin was granted European approval for use in combination with paclitaxel in metastatic breast cancer in March 2007. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2519613</comments>
            <pubDate>Fri, 26 Jun 2009 14:00:00 +0100</pubDate>
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        <item>
            <title>Roche Files MabThera as a First-line Biologic Treatment for Rheumatoid Arthritis in Europe</title>
            <link>http://www.medworm.com/index.php?rid=2516416&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-06-26.htm</link>
            <description>Roche announced today that it has submitted a combined filing to the European health authorities (the European Medicines Agency) for three new indications to extend the label for MabThera to use as a first-line biologic therapy for patients with rheumatoid arthritis (RA). The new filings are for patients who have not been treated with methotrexate (MTX), the current standard treatment option; those who have had an inadequate response to MTX; and for the prevention of joint damage across all RA patient populations. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2516416</comments>
            <pubDate>Fri, 26 Jun 2009 05:00:00 +0100</pubDate>
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        <item>
            <title>Roche&amp;#039;s Half Year Results for 2009</title>
            <link>http://www.medworm.com/index.php?rid=2494173&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-06-23.htm</link>
            <description>Roche will publish its Half Year Results for 2009 prior to the opening of the Swiss Stock Exchange on July 23 at 7.00 CET / 6.00 GMT / 1.00 AM EDT / 22.00 PM PDT (evening before). (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2494173</comments>
            <pubDate>Tue, 23 Jun 2009 08:00:00 +0100</pubDate>
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        <item>
            <title>New data demonstrate the ability of MabThera to reduce the progression of joint damage when used as a first-line biologic treatment in rheumatoid arthritis</title>
            <link>http://www.medworm.com/index.php?rid=2481854&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-06-11.htm</link>
            <description>RA patients with enhanced response identified. New data show for the first time that a course of 2 infusions of MabThera 1000mg (rituximab, known as Rituxan within the United States) given every 24 weeks as the patient&amp;#8217;s first biologic can significantly slow down joint damage following 1 year of treatment, with virtually no progression of joint damage seen from six months. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2481854</comments>
            <pubDate>Thu, 11 Jun 2009 08:15:00 +0100</pubDate>
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        <item>
            <title>Reminder: Roche Investor Science Event: Conference call from EULAR 2009</title>
            <link>http://www.medworm.com/index.php?rid=2481855&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-06-11b.htm</link>
            <description>We are pleased to invite you to a Conference Call to discuss new data on our Rheumatoid Arthritis portfolio being presented during the 2009 EULAR Conference (European League Against Rheumatism), which runs from June 10th &amp;#8211; June 13th, 2009 in Copenhagen, Denmark. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2481855</comments>
            <pubDate>Thu, 11 Jun 2009 08:00:00 +0100</pubDate>
            <guid isPermaLink="false">2481855</guid>        </item>
        <item>
            <title>Reminder: Invitation to Roche Accounting Teleconference</title>
            <link>http://www.medworm.com/index.php?rid=2481856&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-06-11a.htm</link>
            <description>We are pleased to invite you to an accounting conference call followed by Q&amp;#038;A on the impact of the Genentech transaction on the Roche Group&amp;#8217;s consolidated equity. As previously announced, this call will focus on prime accounting implications in order to provide an appropriate baseline for analyst models. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2481856</comments>
            <pubDate>Thu, 11 Jun 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2481856</guid>        </item>
        <item>
            <title>New data reinforces long-term efficacy of ACTEMRA in rheumatoid arthritis across all patient population types</title>
            <link>http://www.medworm.com/index.php?rid=2481857&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-06-10.htm</link>
            <description>Up to 56% of patients with active rheumatoid arthritis (RA) treated with ACTEMRA (tocilizumab, known as RoACTEMRA within the EU) for over two years, will achieve disease remission, according to new data presented today at the European League Against Rheumatism (EULAR) congress. Remission, as defined by DAS28 &amp;#060;2.62, provides real-life benefits to people living with RA by meaningfully improving disease symptoms which help them to continue or regain normal day-to-day functioning. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2481857</comments>
            <pubDate>Tue, 09 Jun 2009 22:01:00 +0100</pubDate>
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        <item>
            <title>Roche to commence phase III trials with innovative treatment designed to lower cardiovascular risk in diabetes patients with recent heart attack</title>
            <link>http://www.medworm.com/index.php?rid=2466362&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-06-09.htm</link>
            <description>Roche today announced it will start Phase III clinical investigations for aleglitazar, its innovative PPAR co-agonist R1439 which is uniquely designed to reduce cardiovascular morbidity and mortality in high risk patients with type 2 diabetes. This decision is supported by data from the Phase II SYNCHRONY study published today in The Lancet and announced at the American Diabetes Association (ADA) in New Orleans, US. The phase III programme is anticipated to start in the second half of 2009. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2466362</comments>
            <pubDate>Tue, 09 Jun 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2466362</guid>        </item>
        <item>
            <title>Invitation to Roche Accounting Teleconference</title>
            <link>http://www.medworm.com/index.php?rid=2466363&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-06-08.htm</link>
            <description>We are pleased to invite you to an accounting conference call followed by Q&amp;#038;A on the impact of the Genentech transaction on the Roche Group&amp;#8217;s consolidated equity. As previously announced, this call will focus on prime accounting implications in order to provide an appropriate baseline for analyst models. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2466363</comments>
            <pubDate>Mon, 08 Jun 2009 08:00:00 +0100</pubDate>
            <guid isPermaLink="false">2466363</guid>        </item>
        <item>
            <title>Reminder: Roche investor science event from ADA 2009</title>
            <link>http://www.medworm.com/index.php?rid=2461391&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-06-05.htm</link>
            <description>We kindly invite investors and analysts to participate in a conference call that will be held during the American Diabetes Association (ADA) 69th Scientific Sessions in New Orleans. On the call, Roche will discuss new phase II data on its PPAR co-agonist aleglitazar (R1439). Further, Roche will provide an overall update on its pipeline and emerging franchise in diabetes and metabolic diseases. The presentation will be followed by a Q&amp;#038;A session. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2461391</comments>
            <pubDate>Fri, 05 Jun 2009 08:30:00 +0100</pubDate>
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        <item>
            <title>IMPACT study shows longer Valcyte treatment provides better protection against cytomegalovirus (CMV) disease</title>
            <link>http://www.medworm.com/index.php?rid=2450982&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-06-02.htm</link>
            <description>New Phase III study results presented for the first time today at the ninth annual American Transplant Congress 2009 (ATC) demonstrate that doubling the duration of preventive therapy (&amp;#8216;prophylaxis&amp;#8217;) with Valcyte (oral valganciclovir), significantly reduces the incidence of CMV disease by 56% in high-risk kidney transplant patients within the first year post-transplant. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2450982</comments>
            <pubDate>Tue, 02 Jun 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2450982</guid>        </item>
        <item>
            <title>Encouraging first data on new targeted treatment for patients with melanoma - the deadliest form of skin cancer</title>
            <link>http://www.medworm.com/index.php?rid=2450983&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-06-01.htm</link>
            <description>Roche announced today results from a phase I study with PLX4032 (R7204) a new, highly selective and promising treatment for patients with advanced melanoma whose cancer harbours the BRAF mutation (known as mutation-positive). Patients treated with PLX4032 lived for a median of at least six months without their disease getting worse and experienced shrinkage of their tumours; this included patients where the cancer had spread to the liver, lung and bone. Historically, metastatic melanoma patients live less than two months before their disease progresses. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2450983</comments>
            <pubDate>Mon, 01 Jun 2009 10:30:00 +0100</pubDate>
            <guid isPermaLink="false">2450983</guid>        </item>
        <item>
            <title>Herceptin landmark study (ToGA) reveals unprecedented survival benefit in HER2-positive stomach cancer</title>
            <link>http://www.medworm.com/index.php?rid=2450984&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-05-31.htm</link>
            <description>Data from the ToGA study presented today at the American Society for Clinical Oncology Annual Meeting in Orlando, Florida showed that adding Herceptin (trastuzumab) to standard chemotherapy (Xeloda or intravenous 5-FU and cisplatin) prolongs the lives of patients with this aggressive cancer on average by nearly three months to 13.8 months. Advanced stomach (gastric) cancer is associated with a poor prognosis; the median survival time after diagnosis is approximately 10 months with currently available therapies. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2450984</comments>
            <pubDate>Sun, 31 May 2009 14:30:00 +0100</pubDate>
            <guid isPermaLink="false">2450984</guid>        </item>
        <item>
            <title>Phase III study showed patients lived longer without advanced lung cancer progressing when Tarceva was added to Avastin as first-line maintenance therapy</title>
            <link>http://www.medworm.com/index.php?rid=2444713&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-05-30b.htm</link>
            <description>Roche today announced that a Phase III study (ATLAS) showed patients with advanced non-small cell lung cancer (NSCLC) who received Tarceva&amp;#174; (erlotinib) in combination with Avastin&amp;#174; (bevacizumab) as first-line maintenance treatment had a 39 percent improvement in the time they lived without the disease advancing (progression-free survival or PFS), compared with those who received Avastin plus placebo (hazard ratio=0.72; p=0.0012). Adverse events were consistent with previous Avastin or Tarceva NSCLC studies, or trials evaluating the two medicines together. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2444713</comments>
            <pubDate>Sat, 30 May 2009 15:00:00 +0100</pubDate>
            <guid isPermaLink="false">2444713</guid>        </item>
        <item>
            <title>Full results from first Phase III study of Avastin in adjuvant colon cancer announced</title>
            <link>http://www.medworm.com/index.php?rid=2444714&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-05-30.htm</link>
            <description>Results suggest future trials may hold promise for Avastin as early-stage colon cancer treatment even though C-08 study does not meet primary endpoint (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2444714</comments>
            <pubDate>Sat, 30 May 2009 13:00:00 +0100</pubDate>
            <guid isPermaLink="false">2444714</guid>        </item>
        <item>
            <title>New form of targeted therapy offers further hope to patients with advanced HER2-positive breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=2438238&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-05-28.htm</link>
            <description>Final results from a phase II study presented at ASCO show that 25% of women with advanced HER2-positive breast cancer experienced remarkable shrinkage of their tumours, when treated with a new agent called trastuzumab-DM1 (T-DM1). (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2438238</comments>
            <pubDate>Thu, 28 May 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2438238</guid>        </item>
        <item>
            <title>Reminder: Roche investor science event from ADA 2009</title>
            <link>http://www.medworm.com/index.php?rid=2438239&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-05-27.htm</link>
            <description>Phase II data on PPAR co-agonist aleglitazar and overall update on Roche&amp;#180;s diabetes &amp;#038; metabolic diseases pipeline (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2438239</comments>
            <pubDate>Wed, 27 May 2009 08:00:00 +0100</pubDate>
            <guid isPermaLink="false">2438239</guid>        </item>
        <item>
            <title>Roche Investor Science Event: Conference call from EULAR 2009</title>
            <link>http://www.medworm.com/index.php?rid=2435205&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-05-26.htm</link>
            <description>We are pleased to invite you to a Conference Call to discuss new data on our Rheumatoid Arthritis portfolio being presented during the 2009 EULAR Conference (European League Against Rheumatism), which runs from June 10th &amp;#8211; June 13th, 2009 in Copenhagen, Denmark. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2435205</comments>
            <pubDate>Tue, 26 May 2009 09:30:00 +0100</pubDate>
            <guid isPermaLink="false">2435205</guid>        </item>
        <item>
            <title>Reminder - Roche Investor Events: ASCO 2009</title>
            <link>http://www.medworm.com/index.php?rid=2435206&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-05-25b.htm</link>
            <description>We are pleased to invite you to two analyst briefings to discuss data presented on the Roche Group&amp;#8217;s oncology products and pipeline at the American Society of Clinical Oncology meeting (ASCO) in Orlando (May 29 &amp;#8211; June 2, 2009). (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2435206</comments>
            <pubDate>Mon, 25 May 2009 08:01:00 +0100</pubDate>
            <guid isPermaLink="false">2435206</guid>        </item>
        <item>
            <title>Two-year data reinforce effectiveness of ACTEMRA in inhibiting joint damage and improving physical function in patients with rheumatoid arthritis</title>
            <link>http://www.medworm.com/index.php?rid=2432946&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-05-25.htm</link>
            <description>Roche announced today that new two-year data from the LITHE study demonstrate that ACTEMRA (tocilizumab, known as RoACTEMRA within the EU) continues to be highly effective at inhibiting joint structural damage and maintaining consistently high remission rates. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2432946</comments>
            <pubDate>Mon, 25 May 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2432946</guid>        </item>
        <item>
            <title>Roche ASCO planner</title>
            <link>http://www.medworm.com/index.php?rid=2425704&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-05-20.htm</link>
            <description>Roche and Genentech will present a large number of abstracts on their broad oncology portfolio at the Annual Meeting of American Society of Clinical Oncology (ASCO) in Orlando on May 29 &amp;#8211; June 2. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2425704</comments>
            <pubDate>Wed, 20 May 2009 08:00:00 +0100</pubDate>
            <guid isPermaLink="false">2425704</guid>        </item>
        <item>
            <title>Genentech and Biogen Idec submit applications to the FDA for Rituxan for most common type of adult leukemia</title>
            <link>http://www.medworm.com/index.php?rid=2420307&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-05-19b.htm</link>
            <description>Genentech, Inc., wholly owned member of the Roche Group (SWX: RO, ROG; OTCQX: RHHBY), and Biogen Idec (Nasdaq: BIIB) today announced that the companies submitted two supplemental Biologics License Applications (sBLAs) to the U.S. Food and Drug Administration (FDA) for Rituxan (rituximab) plus standard chemotherapy for people with previously untreated or treated chronic lymphocytic leukemia (CLL). (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2420307</comments>
            <pubDate>Tue, 19 May 2009 20:00:00 +0100</pubDate>
            <guid isPermaLink="false">2420307</guid>        </item>
        <item>
            <title>Roche Investor Events: ASCO 2009</title>
            <link>http://www.medworm.com/index.php?rid=2420308&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-05-19.htm</link>
            <description>We are pleased to invite you to two analyst briefings to discuss data presented on the Roche Group&amp;#8217;s oncology products and pipeline at the American Society of Clinical Oncology meeting (ASCO) in Orlando (May 29 &amp;#8211; June 2, 2009). (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2420308</comments>
            <pubDate>Tue, 19 May 2009 14:00:00 +0100</pubDate>
            <guid isPermaLink="false">2420308</guid>        </item>
        <item>
            <title>Roche joins forces to innovate toxicity testing and to reduce animal experimentation</title>
            <link>http://www.medworm.com/index.php?rid=2420309&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-05-18.htm</link>
            <description>Today, Roche opened the Joint Science &amp;#038; Technology Laboratory in Basel, where Roche Pharma scientists are using the innovative xCELLigence real-time Cell Analyzer system of Roche Diagnostics to investigate hepatic and cardiac toxicities in vitro. This new technology will improve the predictive value of in vitro assessments of organ toxicity and help to reduce animal testing in toxicity research. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2420309</comments>
            <pubDate>Mon, 18 May 2009 12:30:00 +0100</pubDate>
            <guid isPermaLink="false">2420309</guid>        </item>
        <item>
            <title>Avastin plus commonly used chemotherapies improved progression-free survival in advanced breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=2409801&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-05-15b.htm</link>
            <description>Data from RIBBON 1 study provides efficacy and safety information with different types of chemotherapy (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2409801</comments>
            <pubDate>Thu, 14 May 2009 22:05:00 +0100</pubDate>
            <guid isPermaLink="false">2409801</guid>        </item>
        <item>
            <title>Roche to present major advances with targeted cancer medicines at ASCO</title>
            <link>http://www.medworm.com/index.php?rid=2409803&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-05-15.htm</link>
            <description>More than 500 scientific abstracts to be presented across 20 types of cancers. Results could significantly improve the way cancer is treated for patients with inoperable stomach cancer; advanced melanoma; lung and breast cancers. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2409803</comments>
            <pubDate>Thu, 14 May 2009 22:00:00 +0100</pubDate>
            <guid isPermaLink="false">2409803</guid>        </item>
        <item>
            <title>Roche investor science event from ADA 2009</title>
            <link>http://www.medworm.com/index.php?rid=2409805&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-05-11b.htm</link>
            <description>Phase II data on PPAR co-agonist aleglitazar and overall update on Roche&amp;#039;s diabetes &amp;#038; metabolic diseases pipeline (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
            <type>organizations</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2409805</comments>
            <pubDate>Mon, 11 May 2009 08:00:00 +0100</pubDate>
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            <title>Important New Treatment Option Approved in US for Patients with the Most Aggressive Form of Brain Cancer</title>
            <link>http://www.medworm.com/index.php?rid=2394365&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Fmed-avastin-0050343-200px.jpg</link>
            <description>Roche today announced that the US Food and Drug Administration (FDA) granted accelerated approval of Avastin (bevacizumab) for people with glioblastoma with progressive disease following prior therapy. The new indication for Avastin was granted under the FDA&amp;#8217;s accelerated approval program that allows provisional approval of medicines for cancer or other life-threatening diseases. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
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            <pubDate>Wed, 06 May 2009 05:00:00 +0100</pubDate>
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            <title>Roche Investor Events: ASCO 2009</title>
            <link>http://www.medworm.com/index.php?rid=2394366&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-05-04.htm</link>
            <description>We are pleased to invite you to two analyst briefings to discuss data presented on the Roche Group&amp;#8217;s oncology products and pipeline at the American Society of Clinical Oncology meeting (ASCO) in Orlando (May 29 &amp;#8211; June 2, 2009). (Source: Roche Investor Update)</description>
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            <pubDate>Mon, 04 May 2009 12:00:00 +0100</pubDate>
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            <title>Roche responds to WHO move to influenza pandemic alert phase 5</title>
            <link>http://www.medworm.com/index.php?rid=2378804&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-04-30.htm</link>
            <description>Roche tonight confirms that it has been in contact with the World Health Organization (WHO) following the announcement to move to influenza pandemic alert phase 5. (Source: Roche Investor Update)</description>
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            <pubDate>Thu, 30 Apr 2009 07:30:00 +0100</pubDate>
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            <title>Ground-breaking combination of all-oral agents demonstrates potential as hepatitis C treatment regimen</title>
            <link>http://www.medworm.com/index.php?rid=2372030&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-04-27.htm</link>
            <description>Roche (SWX: RO, ROG; OTCQX: RHHBY), InterMune, Inc. (Nasdaq: ITMN) and Pharmasset (Nasdaq: VRUS) announced the first results from their innovative, interferon-free regimen of direct-acting antiviral (DAA) combination therapy for the treatment of patients chronically infected with the hepatitis C virus (HCV). The study combined two oral DAAs, R7227 (also known as ITMN-191) and R7128, for the first time in patients. There were no serious adverse events reported during the 14 days of dosing, the reductions in levels of HCV RNA were significant. (Source: Roche Investor Update)</description>
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            <pubDate>Mon, 27 Apr 2009 05:00:00 +0100</pubDate>
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            <title>Phase III C-08 study of Avastin in early-stage colon cancer does not meet primary endpoint</title>
            <link>http://www.medworm.com/index.php?rid=2355530&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-04-22.htm</link>
            <description>Roche today announced the results of the first phase III trial evaluating the use of Avastin (bevacizumab) plus chemotherapy (FOLFOX) for the treatment of colon cancer immediately following surgery (adjuvant therapy) compared to chemotherapy alone. (Source: Roche Investor Update)</description>
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            <pubDate>Wed, 22 Apr 2009 05:00:00 +0100</pubDate>
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            <title>Roche strongly outperforms market in first quarter</title>
            <link>http://www.medworm.com/index.php?rid=2336296&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-04-16.htm</link>
            <description>Genentech transaction completed, integration proceeding rapidly (Source: Roche Investor Update)</description>
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            <pubDate>Thu, 16 Apr 2009 05:00:00 +0100</pubDate>
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            <title>Reminder: Roche&amp;#039;s First Quarter Sales 2009 Conference Call</title>
            <link>http://www.medworm.com/index.php?rid=2336297&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-04-15b.htm</link>
            <description>Roche will publish its Sales Results for the 1st Quarter of 2009 prior to the opening of the Swiss Stock Exchange on Thursday 16th April, 2009. (Source: Roche Investor Update)</description>
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            <pubDate>Wed, 15 Apr 2009 08:00:00 +0100</pubDate>
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            <title>Roche Diabetes Care supports &amp;#034;Changing Diabetes in Children&amp;#034;</title>
            <link>http://www.medworm.com/index.php?rid=2336298&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-04-15.htm</link>
            <description>Roche today announced that it will join forces with Novo Nordisk and the World Diabetes Foundation (WDF) in Novo Nordisk&amp;#8217;s five-year program called &amp;#8220;Changing Diabetes in Children&amp;#8221;. Roche Diabetes Care will actively endorse humanitarian activities in this project which is starting in Tanzania, Uganda, Cameroon, Guinea-Conakry and the Democratic Republic of Congo. (Source: Roche Investor Update)</description>
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            <pubDate>Wed, 15 Apr 2009 06:45:00 +0100</pubDate>
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            <title>Roche and Genentech announce organizational and leadership decisions</title>
            <link>http://www.medworm.com/index.php?rid=2336299&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-04-14.htm</link>
            <description>Following the completion of the Genentech transaction Roche (SWX: ROG.VX; RO.S, OTCQX: RHHBY) today announced the successful start of the integration. Building on the long-standing and trustful relationship of the two companies, senior leaders from Genentech and Roche have made considerable progress in a short period of time to set the course for the integration. (Source: Roche Investor Update)</description>
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            <pubDate>Tue, 14 Apr 2009 21:00:00 +0100</pubDate>
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            <title>Roche and Genentech announce voluntary withdrawal of Raptiva from the U.S. market</title>
            <link>http://www.medworm.com/index.php?rid=2313877&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-04-08.htm</link>
            <description>Roche and Genentech, Inc. announced today a phased voluntary withdrawal of the psoriasis drug Raptiva (efalizumab) from the U.S. market. (Source: Roche Investor Update)</description>
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            <pubDate>Wed, 08 Apr 2009 20:30:00 +0100</pubDate>
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            <title>Presentational changes of Roche&amp;#039;s quarterly sales results</title>
            <link>http://www.medworm.com/index.php?rid=2313878&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-04-07.htm</link>
            <description>As announced earlier, the Roche Group will publish its first quarter sales results on 16 April 2009. To reflect the Pharmaceuticals Division&amp;#8217;s integrated organisation following the buy-out of Genentech non-controlling interests, the Pharmaceuticals Division&amp;#8217;s results will in future be reported by region and not by sub-division as previously. (Source: Roche Investor Update)</description>
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            <pubDate>Tue, 07 Apr 2009 05:00:00 +0100</pubDate>
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            <title>Roche to introduce new LightCycler MRSA Advanced Test in the EU</title>
            <link>http://www.medworm.com/index.php?rid=2313879&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-04-02.htm</link>
            <description>Roche announced today that its new LightCycler test for the detection of methicillin-resistant Staphylococcus aureus (MRSA) is now available with the CE Mark, allowing it to be sold for clinical use in the European Union. (Source: Roche Investor Update)</description>
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            <pubDate>Thu, 02 Apr 2009 05:00:00 +0100</pubDate>
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            <title>Fda advisory committee unanimously recommends accelerated approval of avastin for previously treated brain cancer (glioblastoma)</title>
            <link>http://www.medworm.com/index.php?rid=2313880&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-04-01.htm</link>
            <description>Genentech, Inc. announced today that the U.S. Food and Drug Administration (FDA) Oncologic Drugs Advisory Committee (ODAC) voted unanimously that the response seen with Avastin (bevacizumab) in people with previously treated glioblastoma is of sufficient magnitude to be reasonably likely to predict clinical benefit. The FDA is expected to make a decision whether to grant accelerated approval of Avastin for use in this most aggressive form of brain cancer by May 5, 2009. (Source: Roche Investor Update)</description>
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            <pubDate>Wed, 01 Apr 2009 05:30:00 +0100</pubDate>
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            <title>Avastin label updated reflecting confidence in safety profile</title>
            <link>http://www.medworm.com/index.php?rid=2313881&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-03-31.htm</link>
            <description>The European Medicines Agency (EMEA) has removed a restriction in the product label which prevented the use of Avastin (bevacizumab) in some patients whose primary cancer has spread to their brain (brain metastases). (Source: Roche Investor Update)</description>
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            <pubDate>Tue, 31 Mar 2009 15:30:00 +0100</pubDate>
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            <title>Roche completes acquisition of Genentech</title>
            <link>http://www.medworm.com/index.php?rid=2313882&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-03-26b.htm</link>
            <description>Roche (SWX: ROG.VX; RO.S, OTCQX: RHHBY) and Genentech announced today that Roche has completed its acquisition of Genentech pursuant to a short-form merger in which Genentech became a wholly-owned member of the Roche Group. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
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            <pubDate>Thu, 26 Mar 2009 16:30:00 +0100</pubDate>
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            <title>Roche completes tender offer for Genentech</title>
            <link>http://www.medworm.com/index.php?rid=2290626&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-03-26.htm</link>
            <description>Roche (SWX: ROG.VX; RO.S, OTCQX: RHHBY) announced today that its wholly-owned subsidiary, Roche Investments USA Inc., completed its tender offer for the publicly held shares of Genentech (NYSE: DNA). The offer expired at midnight, New York City time, at the end of Wednesday, March 25. A total of approximately 395.7 million shares of Genentech common stock were tendered representing 84.7% of Genentech&amp;#8217;s publicly held shares. Roche Investments USA Inc. has accepted for payment all shares validly tendered pursuant to its tender offer. (Source: Roche Investor Update)</description>
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            <pubDate>Thu, 26 Mar 2009 06:00:00 +0100</pubDate>
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            <title>RiskMetrics Group Recommends Genentech Shareholders Accept Roche&amp;#039;s $95.00 per Share Cash Tender Offer</title>
            <link>http://www.medworm.com/index.php?rid=2290627&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-03-24.htm</link>
            <description>Roche (SWX: ROG.VX; RO.S, OTCQX: RHHBY) announced today that RiskMetrics Group, Inc., a leading provider of risk and corporate governance services to participants in the global financial markets, recommends that Genentech (NYSE: DNA) shareholders tender their shares to Roche at $95.00 per share. (Source: Roche Investor Update)</description>
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            <pubDate>Tue, 24 Mar 2009 16:30:00 +0100</pubDate>
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            <title>Roche announces filing of Tarceva in EU as first-line maintenance therapy in advanced non-small cell lung cancer</title>
            <link>http://www.medworm.com/index.php?rid=2279607&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-03-19.htm</link>
            <description>Today, Roche submitted an extension of the Marketing Authorisation Application to the European Medicines Agency (EMEA) for the use of Tarceva (erlotinib) as a first-line maintenance treatment - immediately following initial treatment with platinum-based chemotherapy - for patients with advanced non-small cell lung cancer (NSCLC) who have not progressed in their disease. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
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            <pubDate>Thu, 19 Mar 2009 06:00:00 +0100</pubDate>
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            <title>Roche&amp;#039;s First Quarter Sales 2009 Conference Call</title>
            <link>http://www.medworm.com/index.php?rid=2279608&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-03-18b.htm</link>
            <description>Roche will publish its Sales Results for the 1st Quarter of 2009 prior to the opening of the Swiss Stock Exchange on Thursday 16th April, 2009. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
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            <pubDate>Wed, 18 Mar 2009 09:00:00 +0100</pubDate>
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            <title>Herceptin now shown to significantly prolong the lives of patients with HER2-positive advanced stomach cancer</title>
            <link>http://www.medworm.com/index.php?rid=2279609&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-03-18.htm</link>
            <description>Roche today announced results from a major international study which show that adding Herceptin (trastuzumab) to standard chemotherapy significantly prolongs lives of patients with HER2-positive stomach (gastric) cancer. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
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            <pubDate>Wed, 18 Mar 2009 06:00:00 +0100</pubDate>
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            <title>Roche and Genentech reach a friendly agreement to combine the two organizations and create a leader in healthcare innovation</title>
            <link>http://www.medworm.com/index.php?rid=2265563&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-03-12.htm</link>
            <description>Roche (SWX: ROG.VX; RO.S) and Genentech (NYSE: DNA) announced today that they signed a merger agreement under which Roche will acquire the outstanding publicly held interest in Genentech for US$95.00 per share in cash, or a total payment of approximately US$46.8 billion to equity holders of Genentech other than Roche. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
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            <pubDate>Thu, 12 Mar 2009 06:00:00 +0100</pubDate>
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            <title>Herceptin proven to benefit women with HER2 positive early breast cancer - latest results from the HERA study</title>
            <link>http://www.medworm.com/index.php?rid=2253521&amp;cid=s_37969_34_f&amp;fid=37969&amp;url=http%3A%2F%2Fwww.roche.com%2Fen%2Finvestors%2Fir_update%2Finv-update-2009-03-11.htm</link>
            <description>The Breast International Group (BIG) in collaboration with Roche announced today that women with HER2 positive early breast cancer continue to benefit from Herceptin (trastuzumab) several years after treatment completion and as a result enjoy a longer life disease free. The patients were treated for one year with Herceptin and followed up for four years. These data from the HERA study were presented at the Primary Therapy in Early Breast Cancer conference in St. Gallen, Switzerland. (Source: Roche Investor Update)</description>
            <author>Roche Investor Update</author>
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            <pubDate>Wed, 11 Mar 2009 06:00:00 +0100</pubDate>
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