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        <title>GSK news 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 'GSK news' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=GSK+news&t=GSK+news&s=Search&f=source]]></link>
        <lastBuildDate>Mon, 06 Feb 2012 01:21:51 +0100</lastBuildDate>
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            <title>GSK joins new global partnership to help defeat ten neglected tropical diseases by 2020</title>
            <link>http://www.medworm.com/index.php?rid=5651578&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2012%2F2012-pressrelease-875381.htm</link>
            <description>(Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
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            <pubDate>Mon, 30 Jan 2012 10:24:27 +0100</pubDate>
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            <title>GSK announces changes to the Board</title>
            <link>http://www.medworm.com/index.php?rid=5639971&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2012%2F2012-pressrelease-871327.htm</link>
            <description>GlaxoSmithKline plc today announced that at the company’s Annual General Meeting (AGM) in 2013, following nine years of respective service to the GSK Board, Sir Crispin Davis, Sir Robert Wilson and Mr Larry Culp will not stand for re-election to the Board. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Fri, 27 Jan 2012 11:07:11 +0100</pubDate>
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            <title>GSK responds to the recent court ruling on the COMPAS study in Mendoza, Argentina</title>
            <link>http://www.medworm.com/index.php?rid=5586177&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2012%2F2012-pressrelease-844572.htm</link>
            <description>(Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Wed, 11 Jan 2012 12:29:01 +0100</pubDate>
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            <title>GSK and Theravance announce initial outcomes from pivotal Phase III studies for once-daily RelovairTM* in COPD and asthma</title>
            <link>http://www.medworm.com/index.php?rid=5586178&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2012%2F2012-pressrelease-840683.htm</link>
            <description>GlaxoSmithKline (GSK) and Theravance, Inc. (NASDAQ: THRX) today announced the completion of the phase III registration programme for the once-daily investigational medicine Relovair™* (fluticasone furoate “FF”/vilanterol “VI”) in patients with chronic obstructive pulmonary disease (COPD) and of all but one of the pivotal studies in patients with asthma. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Mon, 09 Jan 2012 07:17:32 +0100</pubDate>
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            <title>GlaxoSmithKline provides update on divestment of non-core over-the-counter (OTC) brands</title>
            <link>http://www.medworm.com/index.php?rid=5527943&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-821642.htm</link>
            <description>In February 2011 GSK announced its intention to divest non-core Consumer Healthcare OTC products predominantly in the United States and Europe with aggregate annual sales of approximately £500 million. The proposed divestment is designed to realise value for shareholders and simplify GSK’s Consumer Healthcare business and allow it to focus on its priority brands and markets. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Tue, 20 Dec 2011 13:32:07 +0100</pubDate>
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            <title>GSK extends pneumococcal vaccine agreement with GAVI Alliance</title>
            <link>http://www.medworm.com/index.php?rid=5507599&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-815404.htm</link>
            <description>GSK today announced it has expanded its agreement with the GAVI Alliance in a move to help protect millions more children in the world‟s poorest countries from pneumococcal disease. Pneumococcal disease can lead to pneumonia, meningitis and sepsis and is a leading cause of death in children under the age of five in developing countries. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Fri, 16 Dec 2011 12:10:27 +0100</pubDate>
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            <title>GlaxoSmithKline and Human Genome Sciences initiate phase III trial of belimumab (Benlysta®) administered subcutaneously in subjects with systemic lupus erythematosus</title>
            <link>http://www.medworm.com/index.php?rid=5507600&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-813312.htm</link>
            <description>GlaxoSmithKline (GSK) and Human Genome Sciences, Inc. (Nasdaq: HGSI) today announced that dosing has been initiated in BLISS-SC, a new Phase III trial to evaluate the efficacy, safety and tolerability of BENLYSTA® (belimumab) administered subcutaneously (SC) once-weekly to autoantibody-positive adults with active systemic lupus erythematosus (SLE). (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Thu, 15 Dec 2011 12:59:41 +0100</pubDate>
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            <title>GSK presents phase lll data for lapatinib at San Antonio breast cancer symposium</title>
            <link>http://www.medworm.com/index.php?rid=5489229&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-798637.htm</link>
            <description>Results from TEACH (Tykerb Evaluation After Chemotherapy) were presented today at the 2011 CRTC-AACR San Antonio Breast Cancer Symposium. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Thu, 08 Dec 2011 22:45:00 +0100</pubDate>
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            <title>GSK and Help for Heroes partner to support the rehabilitation of wounded servicemen and women in the UK</title>
            <link>http://www.medworm.com/index.php?rid=5479025&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-793122.htm</link>
            <description>GSK and Help for Heroes today announced a new partnership to help support injured British armed forces personnel successfully transition back into civilian life. The partnership will focus on the creation of a specialist 'Wellness Centre' at Tedworth House, a Help for Heroes Personnel Recovery and Assessment Centre located in Wiltshire. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Wed, 07 Dec 2011 09:14:33 +0100</pubDate>
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            <title>GSK statement in response to the Prime Minister’s speech on life sciences</title>
            <link>http://www.medworm.com/index.php?rid=5479026&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-789508.htm</link>
            <description>“The Government’s strategy for Life Sciences is a very important next step on the journey to make the UK the best place in the world to locate pharmaceutical investment. The actions on research and manufacturing will further strengthen the attractiveness of the UK and most importantly the results of the Innovation Review should ensure that the NHS is a stronger adopter of innovative medicines and technology, ensuring that all patients can benefit from cost-effective treatments and interventions approved by NICE. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Mon, 05 Dec 2011 14:31:53 +0100</pubDate>
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            <title>Regulatory Update: GlaxoSmithKline submits additional information for candidate meningococcal and Hib combination vaccine</title>
            <link>http://www.medworm.com/index.php?rid=5460725&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-781571.htm</link>
            <description>GlaxoSmithKline [NYSE:GSK] today submitted additional information to the U.S. Food and Drug Administration (FDA) in support of the Biologics License Application (BLA) for the candidate meningococcal and Hib combination vaccine MenHibrix® (Hib-MenCY-TT). This information was submitted in response to the September 2011 Complete Response letter received from the FDA. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Thu, 01 Dec 2011 14:15:51 +0100</pubDate>
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            <title>Reporting on a core earnings basis will begin with effect from Q1 2012</title>
            <link>http://www.medworm.com/index.php?rid=5460726&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-781224.htm</link>
            <description>As previously announced, GlaxoSmithKline will be introducing core measures for both operating profit and earnings per share to report the performance of the Group with effect from Q1 2012.   (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Thu, 01 Dec 2011 12:10:59 +0100</pubDate>
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            <title>GSK welcomes GAVI Alliance decision to introduce vaccines against cervical cancer and rubella in the world’s poorest countries</title>
            <link>http://www.medworm.com/index.php?rid=5424407&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-747562.htm</link>
            <description>GlaxoSmithKline today welcomed the decision of the GAVI Board to provide funding to facilitate the provision of cervical cancer immunisation programmes and rubella vaccination, across the world’s poorest countries. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Thu, 17 Nov 2011 12:48:09 +0100</pubDate>
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            <title>GlaxoSmithKline welcomes innovative knowledge-sharing collaboration to break deadlock in antibiotic discovery and development</title>
            <link>http://www.medworm.com/index.php?rid=5424408&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-745639.htm</link>
            <description>GlaxoSmithKline (GSK) today welcomes the European Commission’s commitment to promote collaborative research efforts to develop new antibiotics against the growing threat from resistant bacteria. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Thu, 17 Nov 2011 10:17:00 +0100</pubDate>
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            <title>GSK receives initial data from the first completed phase lll study of albiglutide in type 2 diabetes</title>
            <link>http://www.medworm.com/index.php?rid=5411947&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-742869.htm</link>
            <description>GlaxoSmithKline (GSK) today announced that topline results have been received from the first of eight Phase III studies of albiglutide to complete in type 2 diabetes. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
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            <pubDate>Wed, 16 Nov 2011 12:05:59 +0100</pubDate>
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            <title>Data published in The Lancet Oncology support high efficacy previously demonstrated by Cervarix® (HPV 16 and 18 vaccine) against precancerous cervical lesions caused by HPV 16 and 18 and also efficacy against certain other cancer-causing HPV types</title>
            <link>http://www.medworm.com/index.php?rid=5391461&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-723785.htm</link>
            <description>An analysis published today in The Lancet Oncology reinforces previous findings showing that GlaxoSmithKline’s Cervarix®, provided protection against advanced precancerous lesions (CIN3+), above that expected from a vaccine that protects against human papillomavirus (HPV) types 16 and 18. CIN3+ is the immediate step before invasive cervical cancer and data showing protection against this type of lesion are considered the most stringent evidence of potential cervical cancer prevention. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Wed, 09 Nov 2011 09:16:01 +0100</pubDate>
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            <title>GSK presents phase III results for eltrombopag in hepatitis C virus related thrombocytopenia</title>
            <link>http://www.medworm.com/index.php?rid=5391462&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-721916.htm</link>
            <description>Findings from the ENABLE clinical trials, which evaluated the ability of eltrombopag to raise and maintain platelet levels in patients with chronic hepatitis C virus (HCV) infection and low platelet levels that would preclude initiation of interferon-based antiviral therapy, were presented today at the 62nd Annual Meeting of the American Association for the Study of Liver Diseases in San Francisco. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Mon, 07 Nov 2011 20:49:58 +0100</pubDate>
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            <title>GlaxoSmithKline reaches agreement in principle to resolve multiple investigations with US Government</title>
            <link>http://www.medworm.com/index.php?rid=5367737&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-710182.htm</link>
            <description>GSKannounced that it has reached an agreement in principle with the US Government to conclude the Company’s most significant ongoing Federal government investigations, specifically: the investigation into GSK’s sales and marketing practices begun by the US Attorney’s office of Colorado in 2004 and later taken over by the US Attorney’s Office of Massachusetts;  the U.S. Department of Justice’s investigation of possible inappropriate use of the nominal price exception  under the Medicaid Rebate Program;  and the Department of Justice’s investigation of the development and marketing of Avandia. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Thu, 03 Nov 2011 07:00:00 +0100</pubDate>
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            <title>GSK delivers strong Q3 performance with underlying sales growth of 6% and reported sales growth of 3%</title>
            <link>http://www.medworm.com/index.php?rid=5350690&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-692882.htm</link>
            <description>(Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Wed, 26 Oct 2011 10:38:58 +0100</pubDate>
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            <title>GSK joins WIPO Re:Search open innovation platform as part of its commitment to tackling diseases of the developing world</title>
            <link>http://www.medworm.com/index.php?rid=5350691&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-692768.htm</link>
            <description>GlaxoSmithKline (GSK) today announced it has joined WIPO Re:Search as part of its open innovation strategy to help accelerate the development of new and better treatments against neglected tropical diseases (NTDs) which affect more than a billion people in the world’s poorest countries each year. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Wed, 26 Oct 2011 09:00:00 +0100</pubDate>
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            <title>First results from ongoing Phase III trial show malaria vaccine candidate, RTS,S* reduces the risk of malaria by half in African children aged 5 to 17 months</title>
            <link>http://www.medworm.com/index.php?rid=5326189&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-676305.htm</link>
            <description>First results from a large-scale Phase III trial of RTS,S, published online today in the New England Journal of Medicine (NEJM), show the malaria vaccine candidate to provide young African children with significant protection against clinical and severe malaria with an acceptable safety and tolerability profile. The results were announced today at the Malaria Forum hosted by the Bill &amp; Melinda Gates Foundation in Seattle, Washington. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Tue, 18 Oct 2011 17:00:00 +0100</pubDate>
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            <title>Regulatory Update:  GlaxoSmithKline receives Complete Response letter from FDA for candidate meningococcal and Hib combination vaccine</title>
            <link>http://www.medworm.com/index.php?rid=5253358&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-636304.htm</link>
            <description>GlaxoSmithKline [NYSE:GSK] announced today that it has received a Complete Response letter from the U.S. Food and Drug Administration (FDA) for the Biologics License Application (BLA) for the candidate meningococcal and Hib combination vaccine, MenHibrix® (Hib-MenCY-TT). (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Fri, 23 Sep 2011 20:52:32 +0100</pubDate>
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            <title>Lucozade to help drive Vodafone McLaren Mercedes performance</title>
            <link>http://www.medworm.com/index.php?rid=5241301&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-633494.htm</link>
            <description>Ahead of this weekend’s Singapore Grand Prix, Lucozade – the UK’s leading sports and energy drink – today announces an innovative performance partnership with the Vodafone McLaren Mercedes Formula 1 team. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Thu, 22 Sep 2011 09:35:17 +0100</pubDate>
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            <title>GlaxoSmithKline (GSK) and McLaren Group announce innovative strategic partnership</title>
            <link>http://www.medworm.com/index.php?rid=5229051&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-625498.htm</link>
            <description>GlaxoSmithKline (GSK) today announced that it has formed a long term strategic partnership with McLaren Group. The partnership, which will run initially until 2016, brings together two UK companies focused on innovation and high-tech research. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Thu, 15 Sep 2011 07:19:42 +0100</pubDate>
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            <title>GlaxoSmithKline (GSK) commits $1 million in cervical cancer vaccine to new cooperative effort aimed at reducing deaths from women's cancers</title>
            <link>http://www.medworm.com/index.php?rid=5229052&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-621052.htm</link>
            <description>GlaxoSmithKline (GSK) today announced that it has committed $1 million in Cervarix® cervical cancer vaccine to the Pink Ribbon Red Ribbon partnership over the next five years. GSK has also pledged $50,000 to support the program operations. As a result of this donation, more than 10,000 girls and women will have access to vaccination. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Tue, 13 Sep 2011 14:58:40 +0100</pubDate>
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            <title>GlaxoSmithKline and Amicus Therapeutics commence second phase III study of Amigal™ for Fabry disease</title>
            <link>http://www.medworm.com/index.php?rid=5212896&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-617531.htm</link>
            <description>GlaxoSmithKline (GSK) and Amicus Therapeutics today announced the first patient has commenced dosing in a Phase III global registration study (Study 012) to compare the safety and efficacy of Amigal™ (migalastat HCl) and enzyme replacement therapy (ERT) for the treatment of Fabry disease. The randomised, open-label, 18-month study will provide longer-term clinical data comparing migalastat HCl to ERT in patients with Fabry disease, a rare inherited lysosomal storage disorder. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Mon, 12 Sep 2011 11:54:32 +0100</pubDate>
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            <title>GSK gives update on agreement with World Health Organization to support de-worming of school age children in endemic countries</title>
            <link>http://www.medworm.com/index.php?rid=5212897&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-616401.htm</link>
            <description>GlaxoSmithKline (GSK) today announced progress on its commitment to expand the donation of albendazole to the World Health Organization (WHO) to treat school age children at risk of intestinal worms, known as soil-transmitted helminths (STH). An agreement signed today formalises the pledge made by GSK in October 2010 to provide an additional 400 million tablets of albendazole per year to WHO to enable de-worming of school age children in Africa. Today’s agreement also provides for albendazole donations to be made to STH endemic countries around the world beyond Africa to ensure the greatest possible benefit is derived from this donation. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Mon, 12 Sep 2011 08:18:47 +0100</pubDate>
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        <item>
            <title>Lapatinib clinical trial update</title>
            <link>http://www.medworm.com/index.php?rid=5212898&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-614837.htm</link>
            <description>This study is fully recruited and the remaining three arms of the trial will continue as planned. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5212898</comments>
            <pubDate>Fri, 09 Sep 2011 11:03:41 +0100</pubDate>
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        <item>
            <title>Jens Eckstein named President of SR One, GSK’s venture healthcare group</title>
            <link>http://www.medworm.com/index.php?rid=5198716&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-609333.htm</link>
            <description>Jens Eckstein has been named President of SR One, GSK’s independent healthcare venture organisation, effective 1 October.  Jens will report to R&amp;D Chairman Moncef Slaoui and be based in Boston. He replaces Christoph Westphal, who will be leaving GSK at the end of the year to focus on external business interests, including the Longwood Founder’s Fund, in which GSK is an investor. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5198716</comments>
            <pubDate>Wed, 07 Sep 2011 16:05:35 +0100</pubDate>
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        <item>
            <title>GlaxoSmithKline (GSK) shows sign of things to come at London 2012 Olympic and Paralympic Games</title>
            <link>http://www.medworm.com/index.php?rid=5198717&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-588754.htm</link>
            <description>British Olympic Gold medallist Rebecca Romero today unveiled the biggest 2012 logo on the side of GSK’s headquarters in London. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5198717</comments>
            <pubDate>Wed, 07 Sep 2011 08:27:00 +0100</pubDate>
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        <item>
            <title>GSK awarded contract by BARDA to support research on potential novel antibiotic</title>
            <link>http://www.medworm.com/index.php?rid=5198718&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-606905.htm</link>
            <description>GSK and the Biomedical Advanced Research and Development Authority (BARDA) have agreed to a contract that will support the development by GSK of a potentially new antibiotic against both hospital Gram negative and biothreat pathogens. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5198718</comments>
            <pubDate>Tue, 06 Sep 2011 21:32:10 +0100</pubDate>
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        <item>
            <title>GSK takes minority stake in new spin out Autifony Therapeutics</title>
            <link>http://www.medworm.com/index.php?rid=5149525&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-587067.htm</link>
            <description>GlaxoSmithKline plc today announced that its wholly-owned subsidiary Glaxo Group Limited (GSK) will receive a 25.4% minority equity stake, representing a £1,250,000 investment, in Autifony Therapeutics Limited, a UK-based biotechnology start up created through a funding round of up to £10 million alongside investors Imperial Innovations and SV Life Sciences. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5149525</comments>
            <pubDate>Mon, 22 Aug 2011 07:30:48 +0100</pubDate>
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        <item>
            <title>GSK and Impax announce positive topline results of ASCEND-PD Phase III study of IPX066 in Advanced Parkinson’s disease</title>
            <link>http://www.medworm.com/index.php?rid=5127853&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-580727.htm</link>
            <description>GlaxoSmithKline (GSK) and Impax Pharmaceuticals, the branded products division of Impax Laboratories, Inc. (NASDAQ: IPXL) today announced top-line results of the ASCEND-PD Phase III clinical study of IPX066 versus carbidopa-levodopa plus entacapone (CLE), in patients with advanced Parkinson’s disease (PD). IPX066 is an extended release capsule formulation of carbidopa-levodopa (CD-LD) under investigation for the treatment of the motor symptoms of PD. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5127853</comments>
            <pubDate>Mon, 15 Aug 2011 11:23:37 +0100</pubDate>
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        <item>
            <title>GSK and Enigma Diagnostics announce collaboration on assay development and commercialisation of Enigma’s ML platform</title>
            <link>http://www.medworm.com/index.php?rid=5112561&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-576592.htm</link>
            <description>GlaxoSmithKline (GSK) and Enigma Diagnostics Limited today announced that they have signed agreements for the supply and commercialisation on an exclusive basis of the Enigma® ML system in Europe and other designated key countries, including India, Brazil and Russia. The agreements include development by Enigma of an initial range of respiratory tests for use on its real-time Polymerase Chain Reaction (PCR) technology platform, and provide GSK the opportunity to generate revenues from further test developments in infectious diseases and in other therapeutic areas relevant to its healthcare business. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5112561</comments>
            <pubDate>Wed, 10 Aug 2011 13:38:29 +0100</pubDate>
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        <item>
            <title>Regulatory Update: GSK and XenoPort submit supplemental New Drug Application to FDA for Horizant™ in postherpetic neuralgia</title>
            <link>http://www.medworm.com/index.php?rid=5112562&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-573605.htm</link>
            <description>GlaxoSmithKline (NYSE and LSE: GSK) and XenoPort, Inc. (Nasdaq: XNPT) announced today that a supplemental New Drug Application (sNDA) has been submitted to the U.S. Food and Drug Administration (FDA) requesting approval of Horizant™ (gabapentin enacarbil) Extended-Release Tablets for the management of postherpetic neuralgia (PHN) in adults.  The sNDA has been submitted to the FDA by GSK. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5112562</comments>
            <pubDate>Tue, 09 Aug 2011 20:35:59 +0100</pubDate>
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            <title>Regulatory update – Stiefel, a GSK company, files NDA for tazarotene foam</title>
            <link>http://www.medworm.com/index.php?rid=5090423&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-560149.htm</link>
            <description>Stiefel, a GSK company, announced today that it has submitted a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA), for tazarotene foam for the topical treatment of facial acne vulgaris in patients 12 years of age or older. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5090423</comments>
            <pubDate>Wed, 03 Aug 2011 13:11:16 +0100</pubDate>
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        <item>
            <title>GSK delivers strong Q2 performance with underlying sales growth* of 5%, increased pipeline visibility and dividend of 16p, up 7%</title>
            <link>http://www.medworm.com/index.php?rid=5065576&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-542439.htm</link>
            <description>GSK Q2 results 2011 (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5065576</comments>
            <pubDate>Tue, 26 Jul 2011 09:31:23 +0100</pubDate>
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        <item>
            <title>GlaxoSmithKline European regulatory update on Pandemrix™</title>
            <link>http://www.medworm.com/index.php?rid=5043457&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-537971.htm</link>
            <description>GlaxoSmithKline (GSK) announced today that the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) has recommended an update to the product label for the H1N1 influenza vaccine, Pandemrix. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5043457</comments>
            <pubDate>Thu, 21 Jul 2011 15:07:33 +0100</pubDate>
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        <item>
            <title>GlaxoSmithKline and Human Genome Sciences receive European authorisation for Benlysta® (belimumab)</title>
            <link>http://www.medworm.com/index.php?rid=5032420&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-525094.htm</link>
            <description>GlaxoSmithKline (GSK) and Human Genome Sciences, Inc. (Nasdaq: HGSI) announced today that the European Commission (EC) has granted marketing authorisation for Benlysta® (belimumab) 10mg/kg as an add-on therapy in adult patients with active autoantibody-positive systemic lupus erythematosus (SLE), with a high degree of disease activity (e.g. positive anti-dsDNA and low complement), despite standard therapy. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5032420</comments>
            <pubDate>Thu, 14 Jul 2011 10:42:58 +0100</pubDate>
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        <item>
            <title>EU and US Regulatory Update - Votrient® (pazopanib)</title>
            <link>http://www.medworm.com/index.php?rid=5002118&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-516914.htm</link>
            <description>GlaxoSmithKline (GSK) announced today that it has submitted a variation to the Marketing Authorisation Application to the European Medicines Agency for Votrient (pazopanib) for the treatment of patients with advanced soft tissue sarcoma who have received prior chemotherapy, or for patients who are unsuited for such therapy.   (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5002118</comments>
            <pubDate>Wed, 06 Jul 2011 14:33:41 +0100</pubDate>
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        <item>
            <title>London 2012 partner, GlaxoSmithKline, shares scientific expertise with World Anti-Doping Agency to help fight against abuse of drugs in sport</title>
            <link>http://www.medworm.com/index.php?rid=4994990&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-515683.htm</link>
            <description>London 2012 partner GlaxoSmithKline (GSK) today signed a long-term agreement with the World Anti-Doping Agency (WADA) that will help the agency create early detection methods for medicines that have performance-enhancing potential in sport. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4994990</comments>
            <pubDate>Mon, 04 Jul 2011 13:01:46 +0100</pubDate>
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        <item>
            <title>GlaxoSmithKline receives new approval for Rotarix and significant new indication for Lamictal® (lamotrigine) in Japan</title>
            <link>http://www.medworm.com/index.php?rid=4988327&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-514209.htm</link>
            <description>GlaxoSmithKline (GSK) today announced that its rotavirus vaccine has received approval in Japan from the Ministry of Health, Labour and Welfare (MHLW) for use in infants to prevent gastroenteritis caused by rotavirus. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4988327</comments>
            <pubDate>Fri, 01 Jul 2011 12:19:23 +0100</pubDate>
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        <item>
            <title>GSK welcomes external scientists to diseases of the developing world research campus</title>
            <link>http://www.medworm.com/index.php?rid=4979215&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-508935.htm</link>
            <description>External researchers from six medical research organisations have begun work in the GlaxoSmithKline (GSK) ‘open lab’ in Spain, as part of GSK’s experiment to stimulate collaboration in the search for new medicines against diseases of the developing world, such as malaria and drug resistant tuberculosis. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4979215</comments>
            <pubDate>Tue, 28 Jun 2011 11:50:25 +0100</pubDate>
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        <item>
            <title>GSK statement on University of East Anglia study examining health impacts of anticholinergic medicines for over 65s</title>
            <link>http://www.medworm.com/index.php?rid=4963703&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-504553.htm</link>
            <description>Research led by the University of East Anglia has been published in the Journal of the American Geriatrics Society i examining the long term health impacts of anticholinergic medicines, a wide-ranging group of drugs frequently taken by older people. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4963703</comments>
            <pubDate>Fri, 24 Jun 2011 12:02:13 +0100</pubDate>
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        <item>
            <title>GSK statement on agreements with State Attorneys General on former Cidra manufacturing facility</title>
            <link>http://www.medworm.com/index.php?rid=4963704&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-503212.htm</link>
            <description>GlaxoSmithKline (GSK) has agreed to pay $40.75 million, which will be divided among 37 states and the District of Columbia, as part of an agreement reached related to events during the early 2000s at its former manufacturing facility in Cidra, Puerto Rico. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4963704</comments>
            <pubDate>Thu, 23 Jun 2011 14:49:40 +0100</pubDate>
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        <item>
            <title>GSK to purchase Shenzhen Neptunus stake in previously formed joint venture for influenza vaccines in China</title>
            <link>http://www.medworm.com/index.php?rid=4925825&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-470377.htm</link>
            <description>GSK announced that it has entered into an agreement to acquire the remaining 51% equity interest of Neptunus in the JV company, GSKNB, for a total cash consideration of £24 million (US$39 million).  After approval of this agreement by the Peoples Republic of China’s authorities, GSK will become the sole owner of GSKNB.   (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4925825</comments>
            <pubDate>Tue, 14 Jun 2011 07:25:17 +0100</pubDate>
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        <item>
            <title>GlaxoSmithKline and Valeant announce US FDA approval of Potiga™ (ezogabine)</title>
            <link>http://www.medworm.com/index.php?rid=4925826&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-468753.htm</link>
            <description>GlaxoSmithKline (NYSE: GSK) and Valeant Pharmaceuticals International, Inc. (NYSE/TSX: VRX) announced today that the U.S. Food and Drug Administration (FDA) has approved Potiga™ (ezogabine) Tablets, a potassium channel opener, as adjunctive treatment of partial-onset seizures in patients aged 18 years and older.         (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4925826</comments>
            <pubDate>Mon, 13 Jun 2011 06:43:53 +0100</pubDate>
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        <item>
            <title>Millions of children in the world’s poorest countries could receive vaccination against rotavirus diarrhoeal disease under new offer made by GSK to the GAVI Alliance</title>
            <link>http://www.medworm.com/index.php?rid=4906953&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-462284.htm</link>
            <description>GSK today announced that it has made a new offer to supply its rotavirus vaccine, RotarixTM, to the GAVI Alliance at $2.50 per dose, a small fraction of developed world prices. This announcement is part of the company’s efforts to increase access to its medicines and vaccines in the world’s poorest countries. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4906953</comments>
            <pubDate>Mon, 06 Jun 2011 09:30:00 +0100</pubDate>
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            <title>GlaxoSmithKline’s pazopanib improved progression free survival in adults with certain soft tissue sarcomas</title>
            <link>http://www.medworm.com/index.php?rid=4906954&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-461982.htm</link>
            <description>Results of the PALETTE (PAzopanib ExpLorEd in SofT-Tissue Sarcoma) study presented at the 2011 Annual Meeting of the American Society for Clinical Oncology demonstrated a statistically significant improvement in the time to first occurrence of tumour progression or death (progression free survival or PFS) for study patients treated with the multi-tyrosine kinase inhibitor pazopanib, compared to placebo. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4906954</comments>
            <pubDate>Sat, 04 Jun 2011 12:00:00 +0100</pubDate>
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        <item>
            <title>GSK and Theravance announce results of two pivotal Phase III studies for Relovair in COPD</title>
            <link>http://www.medworm.com/index.php?rid=4887972&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-461192.htm</link>
            <description>(Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4887972</comments>
            <pubDate>Thu, 02 Jun 2011 11:02:18 +0100</pubDate>
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        <item>
            <title>GSK forms partnership with three leading NGOs to address shortage of frontline healthcare workers in Least Developed Countries (LDCs)</title>
            <link>http://www.medworm.com/index.php?rid=4857183&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-436669.htm</link>
            <description>GlaxoSmithKline (GSK) today announced further progress on its commitment to reinvest 20% of profits made in the Least Developed Countries (LDCs) back into projects that strengthen the healthcare infrastructure in those countries. GSK has formed a new partnership with three leading NGOs to deliver the reinvestments in LDCs: AMREF in East and Southern Africa, CARE International UK in Asia Pacific and Save the Children in West Africa. The shared objective of the investments will be to improve health outcomes by supporting frontline health workers who operate in these countries. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4857183</comments>
            <pubDate>Tue, 24 May 2011 08:10:26 +0100</pubDate>
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        <item>
            <title>GlaxoSmithKline and Human Genome Sciences receive positive opinion in Europe from the CHMP for Benlysta® (belimumab)</title>
            <link>http://www.medworm.com/index.php?rid=4844551&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-434551.htm</link>
            <description>GlaxoSmithKline (GSK) and Human Genome Sciences, Inc. (Nasdaq: HGSI) announced today that the European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) has issued a positive opinion, recommending marketing authorisation for Benlysta® (belimumab) as an add-on therapy in adult patients with active autoantibody-positive systemic lupus erythematosus, with a high degree of disease activity (e.g. positive anti-dsDNA and low complement), despite standard therapy. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4844551</comments>
            <pubDate>Fri, 20 May 2011 10:35:37 +0100</pubDate>
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            <title>Young people’s health charity steps forward to claim top accolade and £35,000</title>
            <link>http://www.medworm.com/index.php?rid=4816275&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-427380.htm</link>
            <description>Tower Hamlets-based charity, Step Forward, has beaten more than 400 organisations from around the UK to be crowned the overall winner of this year’s GlaxoSmithKline (GSK) IMPACT Awards, run in partnership with health think-tank The King’s Fund. The charity picked up their award and £35,000 prize at a ceremony last night, held at London’s Science Museum. (Source: GSK news)</description>
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            <pubDate>Fri, 13 May 2011 11:13:37 +0100</pubDate>
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            <title>Pharmaceutical industry and university create Manchester Collaborative Centre for Inflammation Research</title>
            <link>http://www.medworm.com/index.php?rid=4816276&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-424268.htm</link>
            <description>GlaxoSmithKline (GSK), The University of Manchester, and AstraZeneca announce today the creation of the Manchester Collaborative Centre for Inflammation Research (MCCIR), a unique collaboration to establish a world-leading translational centre for inflammatory diseases. The project starts out with an initial investment of £5M from each partner over a three year period. (Source: GSK news)</description>
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            <pubDate>Thu, 12 May 2011 00:01:01 +0100</pubDate>
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            <title>GSK Q1 performance demonstrates continued progress with delivery of underlying sales growth, cash generation and pipeline visibility</title>
            <link>http://www.medworm.com/index.php?rid=4755963&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-408360.htm</link>
            <description>. (Source: GSK news)</description>
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            <pubDate>Wed, 27 Apr 2011 10:52:58 +0100</pubDate>
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            <title>Regulatory update – GSK and Valeant respond to FDA on ezogabine</title>
            <link>http://www.medworm.com/index.php?rid=4728280&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-404368.htm</link>
            <description>GlaxoSmithKline (GSK) and Valeant Pharmaceuticals International, Inc. (NYSE/TSX: VRX) submitted on 15 April 2011 the response to the U.S. Food and Drug Administration (FDA) Complete Response letter received on 30 November 2010 for the New Drug Application (NDA) for ezogabine. (Source: GSK news)</description>
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            <pubDate>Mon, 18 Apr 2011 12:13:09 +0100</pubDate>
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            <title>GSK welcomes key agreement to support global preparedness against pandemic influenza</title>
            <link>http://www.medworm.com/index.php?rid=4728281&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-404323.htm</link>
            <description>GlaxoSmithKline (GSK) welcomes the agreement reached at the Open Ended Working Group (OEWG) coordinated by the World Health Organisation (WHO) on a Framework to support global preparedness for a future influenza pandemic. The agreement establishes the principles of an improved process for influenza virus and benefit-sharing between the WHO GISN (Global Influenza Surveillance Network) and industry. (Source: GSK news)</description>
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            <pubDate>Mon, 18 Apr 2011 11:29:35 +0100</pubDate>
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            <title>Regulatory Update:  GlaxoSmithKline submits additional information for candidate meningococcal and Hib combination vaccine</title>
            <link>http://www.medworm.com/index.php?rid=4716726&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-403684.htm</link>
            <description>GlaxoSmithKline [NYSE:GSK] today submitted additional information to the U.S. Food and Drug Administration (FDA) in support of the Biologics License Application (BLA) for the candidate meningococcal and Hib combination vaccine, MenHibrix® (Hib-MenCY-TT). (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Fri, 15 Apr 2011 15:41:00 +0100</pubDate>
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            <title>GSK European regulatory update on Pandemrix™</title>
            <link>http://www.medworm.com/index.php?rid=4716727&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-403553.htm</link>
            <description>GlaxoSmithKline (GSK) announced today that the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) has recommended changes to the product label for Pandemrix. (Source: GSK news)</description>
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            <pubDate>Fri, 15 Apr 2011 11:10:56 +0100</pubDate>
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            <title>Regulatory Update - Tyverb® (lapatinib)</title>
            <link>http://www.medworm.com/index.php?rid=4716728&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-403443.htm</link>
            <description>GlaxoSmithKline plc (GSK) announced today that it has submitted a Marketing Authorisation Application (MAA) to the European Medicines Agency (EMA) for Tyverb (lapatinib) in combination with paclitaxel for the treatment of patients with metastatic breast cancer whose tumours over-express HER2 (ErbB2). Tyverb/Tykerb is approved in over 90 countries including the EU, Switzerland, US, Canada, Japan, Australia and countries in South America and Asia. (Source: GSK news)</description>
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            <pubDate>Fri, 15 Apr 2011 09:02:56 +0100</pubDate>
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            <title>GlaxoSmithKline announces non-core OTC products to be divested</title>
            <link>http://www.medworm.com/index.php?rid=4711572&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-402902.htm</link>
            <description>GSK today identified the non-core OTC brands that it intends to divest as the company focuses its Consumer Healthcare business around a portfolio of fast-growing priority brands and the emerging markets. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Thu, 14 Apr 2011 14:15:13 +0100</pubDate>
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            <title>Unique research alliance expands collaboration opportunities at state-of-the-art medical imaging centre</title>
            <link>http://www.medworm.com/index.php?rid=4700362&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-397993.htm</link>
            <description>The UK research community will soon have access to world-class medical imaging facilities in London with the signing of an agreement today between an alliance of leading London-based universities, the Medical Research Council (MRC) and the pharmaceutical company GlaxoSmithKline (GSK). In a unique partnership, the MRC, Imperial College London, King’s College London and UCL become equal shareholders in a newly created joint venture that assumes responsibility for the facilities and operations at GSK’s Clinical Imaging Centre (CIC). (Source: GSK news)</description>
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            <pubDate>Tue, 12 Apr 2011 10:57:56 +0100</pubDate>
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            <title>GlaxoSmithKline and XenoPort receive FDA approval for Horizant™</title>
            <link>http://www.medworm.com/index.php?rid=4689038&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-392505.htm</link>
            <description>GlaxoSmithKline (NYSE: GSK) and XenoPort, Inc. (Nasdaq: XNPT) announced Wednesday that the U.S. Food and Drug Administration (FDA) has approved Horizant™ (gabapentin enacarbil) Extended-Release Tablets for the treatment of moderate-to-severe primary Restless Legs Syndrome in adults. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Wed, 06 Apr 2011 22:58:29 +0100</pubDate>
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            <title>GSK publishes payments for research, consulting and advising by US healthcare professionals</title>
            <link>http://www.medworm.com/index.php?rid=4673031&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-384520.htm</link>
            <description>GlaxoSmithKline (NYSE:GSK) today published a list of payments made during 2010 for clinical research studies led by U.S. healthcare professionals. Clinical trials are an important step in the lengthy process of discovering and developing new medicines. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Thu, 31 Mar 2011 13:00:00 +0100</pubDate>
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            <title>GlaxoSmithKline confirms Pronova BioPharma reaches agreement with Apotex regarding Lovaza™ US patent litigation</title>
            <link>http://www.medworm.com/index.php?rid=4673032&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-381896.htm</link>
            <description>GlaxoSmithKline (GSK), which has the marketing rights for Lovaza (omega-3-acid ethyl esters) in the US and Puerto Rico, confirmed today that Pronova BioPharma Norge AS, which owns the patents for Lovaza, has entered into an agreement with Apotex Corp. and Apotex Inc. (collectively “Apotex”), to settle their patent litigation in the United States related to Lovaza. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Wed, 30 Mar 2011 08:00:00 +0100</pubDate>
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            <title>GSK and Valeant receive European authorisation for Trobalt (retigabine)</title>
            <link>http://www.medworm.com/index.php?rid=4673033&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-381864.htm</link>
            <description>GlaxoSmithKline (GSK) and Valeant Pharmaceuticals International, Inc. (NYSE &amp; TSX: VRX) announced today that the European Commission has granted marketing authorisation for Trobalt™ (retigabine) as an adjunctive (add-on) treatment of partial onset seizures (a form of epilepsy where a seizure begins in a specific area in one side of the brain), with or without secondary generalisation in adults aged 18 years and above with epilepsy. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
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            <pubDate>Tue, 29 Mar 2011 16:00:00 +0100</pubDate>
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            <title>GSK publishes 2010 Corporate Responsibility Report</title>
            <link>http://www.medworm.com/index.php?rid=4673034&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011-pressrelease-381836.htm</link>
            <description>In its Corporate Responsibility Report published today, GlaxoSmithKline (GSK) reiterated its commitment to building its business on strong values and ethical standards.   (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
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            <pubDate>Mon, 28 Mar 2011 13:00:00 +0100</pubDate>
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            <title>GSK statement on Avodart™ (dutasteride) for prostate cancer risk reduction</title>
            <link>http://www.medworm.com/index.php?rid=4624049&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011_pressrelease_10043.htm</link>
            <description>GlaxoSmithKline (GSK) announced today that it will no longer pursue global approval (marketing authorisation) for the use of Avodart™ (dutasteride) to reduce the risk of prostate cancer.&amp;nbsp; The Company will withdraw applications from regulatory review where procedures are ongoing and, in the limited number of countries where dutasteride is already indicated for use in prostate cancer risk reduction, GSK will work with regulatory agencies to remove this indication from the product’s licence and support physicians to communicate appropriately to patients. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4624049</comments>
            <pubDate>Wed, 23 Mar 2011 14:06:56 +0100</pubDate>
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            <title>GSK announces positive topline results of Phase lll study of IPX066 in advanced Parkinson’s disease</title>
            <link>http://www.medworm.com/index.php?rid=4585414&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2FLibrary%2Fmedia%2Fpressreleases%2F2011%2F2011_pressrelease_10040.htm</link>
            <description>GSK announced positive, top-line results of the ADVANCE-Parkinson’s Disease (PD) Phase III clinical study, conducted by Impax Pharmaceuticals, of IPX066 versus immediate-release carbidopa-levodopa in advanced PD patients experiencing motor fluctuations. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Mon, 14 Mar 2011 20:00:00 +0100</pubDate>
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            <title>GlaxoSmithKline and Tolerx announce phase III DEFEND-1 study of otelixizumab in type 1 diabetes did not meet its primary endpoint</title>
            <link>http://www.medworm.com/index.php?rid=4572401&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2FLibrary%2Fmedia%2Fpressreleases%2F2011%2F2011_pressrelease_10039.htm</link>
            <description>GlaxoSmithKline (GSK) and Tolerx, Inc. today announced that the Phase III DEFEND-1 study of otelixizumab, an investigational humanised anti-CD3 monoclonal antibody, did not meet the primary efficacy endpoint of change in C-peptide at month 12 in patients with new-onset autoimmune type 1 diabetes. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Fri, 11 Mar 2011 14:00:00 +0100</pubDate>
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            <title>GlaxoSmithKline plc appoints two Non-Executive Directors to its Board</title>
            <link>http://www.medworm.com/index.php?rid=4546646&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011_pressrelease_10037.htm</link>
            <description>GlaxoSmithKline plc (GSK) announces that Ms. Judy Lewent and Ms. Stacey Cartwright have been appointed as Non-Executive Directors and will join the Board of the Company with effect from 1st April 2011. On appointment, they will both become members of GSK’s Audit &amp; Risk Committee.&amp;nbsp; Ms. Lewent is the former Executive Vice President and Chief Financial Officer of Merck &amp; Co., Inc. and now serves on the boards of three publicly listed companies and Ms. Cartwright is Executive Vice President, Chief Financial Officer of Burberry Group plc. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Fri, 04 Mar 2011 10:09:19 +0100</pubDate>
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            <title>Regulatory update: Nimenrix® (MenACWY vaccine)</title>
            <link>http://www.medworm.com/index.php?rid=4537773&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011_pressrelease_10036.htm</link>
            <description>GlaxoSmithKline (GSK) announced today that it has submitted a Marketing Authorisation Application (MAA) to the European Medicines Agency (EMA) for its candidate conjugate meningitis vaccine, Nimenrix®, for active immunisation against invasive meningococcal diseases caused by Neisseria meningitidis serogroups A, C, W-135 and Y. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
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            <pubDate>Wed, 02 Mar 2011 11:50:00 +0100</pubDate>
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            <title>GSK outlines new plan to drive recruitment and attract graduate talent in the UK</title>
            <link>http://www.medworm.com/index.php?rid=4537774&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011_pressrelease_10035.htm</link>
            <description>GlaxoSmithKline (GSK) today outlined new plans to encourage talented students graduating from UK universities to consider pursuing a career within the company. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Wed, 02 Mar 2011 08:00:00 +0100</pubDate>
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            <title>Reward for charities bridging gaps in health care provision</title>
            <link>http://www.medworm.com/index.php?rid=4534170&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011_pressrelease_10034.htm</link>
            <description>Ten UK charities have each won £25,000 in recognition of their outstanding contribution to improving health care.&amp;nbsp; The charities beat more than 400 entrants to become winners of this year’s GlaxoSmithKline (GSK) IMPACT Awards, run in partnership with The King’s Fund. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
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            <pubDate>Tue, 01 Mar 2011 14:22:20 +0100</pubDate>
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            <title>World’s first everyday fluoride toothpaste with NovaMin® technology that can repair sensitive teeth</title>
            <link>http://www.medworm.com/index.php?rid=4534171&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011_pressrelease_10033.htm</link>
            <description>GlaxoSmithKline Consumer Healthcare, the maker of leading sensitive toothpaste brand Sensodyne®, today announced&amp;nbsp;a breakthrough in dental care with the launch of new Sensodyne Repair &amp; Protect.&amp;nbsp; The breakthrough formulation, which the company will launch in over 50 European and International markets during 2011, is the first everyday fluoride toothpaste to contain patented NovaMin® technology, which is scientifically proven to repair* sensitive teeth by forming a tooth-like layer over exposed dentine to help continually repair and protect sensitive areas. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4534171</comments>
            <pubDate>Tue, 01 Mar 2011 11:12:10 +0100</pubDate>
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            <title>David Redfern appointed as new Chairman of ViiV Healthcare</title>
            <link>http://www.medworm.com/index.php?rid=4519275&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011_pressrelease_10032.htm</link>
            <description>GlaxoSmithKline (GSK), ViiV Healthcare, and Pfizer today announced the appointment of David Redfern as the new Chairman of the Board for ViiV Healthcare with effect from 1st April 2011, following the retirement of Julian Heslop.&amp;nbsp; David will continue to serve as Chief Strategy Officer at GSK, which owns a majority share in ViiV Healthcare.&amp;nbsp; (Source: GSK news)</description>
            <author>GSK news</author>
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        <comments>http://www.medworm.com/rss/comments.php?id=4519275</comments>
            <pubDate>Fri, 25 Feb 2011 10:13:04 +0100</pubDate>
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            <title>First African country introduces GSK’s pneumococcal vaccine through innovative financing mechanism</title>
            <link>http://www.medworm.com/index.php?rid=4461818&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011_pressrelease_10026.htm</link>
            <description>GlaxoSmithKline (GSK) announced the incorporation of its pneumococcal vaccine into the Kenyan national immunisation programme.&amp;nbsp; Kenya is the first African country to receive pneumococcal vaccines through the innovative financing mechanism known as the Advance Market Commitment (AMC), which is designed to bring heavily discounted vaccines to children living in the world’s poorest countries. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Fri, 11 Feb 2011 16:10:37 +0100</pubDate>
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            <title>GlaxoSmithKline moving to new building at Philadelphia Navy Yard</title>
            <link>http://www.medworm.com/index.php?rid=4447558&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011_us_pressrelease_10011.htm</link>
            <description>GlaxoSmithKline (NYSE:GSK), a leading worldwide research-based pharmaceutical company, and Liberty Property Trust (NYSE:LRY) today announced that GSK has signed a 15.5-year lease for a new building to be developed by Liberty Property Trust and Synterra Partners. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4447558</comments>
            <pubDate>Tue, 08 Feb 2011 20:02:50 +0100</pubDate>
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            <title>GSK revises US Avandia label to include new restrictions on use</title>
            <link>http://www.medworm.com/index.php?rid=4443378&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011_pressrelease_10024.htm</link>
            <description>GlaxoSmithKline (GSK) today announced revised US prescribing information and medication guides for all rosiglitazone-containing medicines (Avandia®, Avandamet® and Avandaryl®) to include additional safety information and restrictions on the use of these medicines. The new label content reflects the US Food and Drug Administration’s review of cardiovascular event data in type 2 diabetes patients treated with Avandia, and follows a meeting of the joint Advisory Committees in July 2010 and a decision in September 2010 by the FDA to restrict access to these medicines. (Source: GSK news)</description>
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            <pubDate>Mon, 07 Feb 2011 16:09:21 +0100</pubDate>
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            <title>GlaxoSmithKline and Human Genome Sciences announce publication of BLISS-52 phase lll study results for Benlysta® in The Lancet</title>
            <link>http://www.medworm.com/index.php?rid=4443379&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011_pressrelease_10023.htm</link>
            <description>GlaxoSmithKline (GSK)&amp;nbsp; and Human Genome Sciences, Inc. (Nasdaq: HGSI) today announced publication of the BLISS-52 study of Benlysta® (belimumab) in autoantibody-positive patients with active systemic lupus erythematosus (SLE) in 
                  The Lancet
                .&amp;nbsp; (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Mon, 07 Feb 2011 11:49:40 +0100</pubDate>
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            <title>GSK results announcement for the fourth quarter</title>
            <link>http://www.medworm.com/index.php?rid=4430546&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2FLibrary%2Fmedia%2Fpressreleases%2F2011_pressrelease_10021.htm</link>
            <description>GSK Q4 and full year results announced (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Thu, 03 Feb 2011 12:00:00 +0100</pubDate>
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            <title>GSK announces the sale of its entire shareholding in Quest Diagnostics</title>
            <link>http://www.medworm.com/index.php?rid=4426189&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2FLibrary%2Fmedia%2Fpressreleases%2F2011%2F2011_us_pressrelease_10010.htm</link>
            <description>GlaxoSmithKline plc (“GSK”) announces that it has sold its entire holding of 30,755,151 shares of common stock in Quest Diagnostics Inc. (“Quest”). The sale comprised a secondary public offering by GSK (the “Offering”) and an accompanying repurchase of shares by Quest (the “Repurchase”). (Source: GSK news)</description>
            <author>GSK news</author>
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        <comments>http://www.medworm.com/rss/comments.php?id=4426189</comments>
            <pubDate>Tue, 01 Feb 2011 23:00:00 +0100</pubDate>
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            <title>GSK and Actelion discontinue clinical development of almorexant</title>
            <link>http://www.medworm.com/index.php?rid=4408232&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2FLibrary%2Fmedia%2Fpressreleases%2F2011%2F2011_pressrelease_10019.htm</link>
            <description>GlaxoSmithKline (GSK) and Actelion Ltd (SIX: ATLN) today announced that clinical development of the Phase III investigational dual orexin receptor antagonist, almorexant, has been discontinued. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4408232</comments>
            <pubDate>Fri, 28 Jan 2011 07:30:00 +0100</pubDate>
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            <title>GlaxoSmithKline announces start of two phase III studies in advanced/metastatic melanoma</title>
            <link>http://www.medworm.com/index.php?rid=4391228&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011_pressrelease_10018.htm</link>
            <description>GlaxoSmithKline (GSK) announced today the start of two global Phase III studies in advanced or metastatic melanoma patients with a BRAF V600 mutation. The studies will separately assess the efficacy and safety of two investigational agents, GSK2118436 and GSK1120212, to determine their individual ability to stop or slow the progression of skin cancer in patients whose tumours contain a BRAF V600 mutation, which occurs in 50 to 60 percent of melanoma patients.Commencement of these studies confirms previously announced plans to progress these assets into Phase III. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Mon, 24 Jan 2011 13:06:58 +0100</pubDate>
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            <title>Regulatory update - GSK and Valeant receive positive opinion in Europe from the CHMP for Trobalt (retigabine)</title>
            <link>http://www.medworm.com/index.php?rid=4391229&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011_pressrelease_10017.htm</link>
            <description>GlaxoSmithKline (GSK) and Valeant Pharmaceuticals International, Inc. (NYSE &amp; TSX: VRX) announced today that the European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) has issued a positive opinion, recommending marketing authorisation for Trobalt™(retigabine) (Source: GSK news)</description>
            <author>GSK news</author>
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        <comments>http://www.medworm.com/rss/comments.php?id=4391229</comments>
            <pubDate>Fri, 21 Jan 2011 11:30:00 +0100</pubDate>
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            <title>GSK and Prosensa announce start of Phase III study of investigational Duchenne Muscular Dystrophy medication</title>
            <link>http://www.medworm.com/index.php?rid=4365767&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011_pressrelease_10016.htm</link>
            <description>GlaxoSmithKline (GSK) and Prosensa today announced that the first patient has commenced treatment in the Phase III clinical study investigating GSK2402968 (`968), in ambulant boys with Duchenne Muscular Dystrophy (DMD), who have a dystrophin gene mutation amenable to an exon 51 skip (up to 13% of boys with DMD). Commencement of this study confirms previously announced plans to progress this asset into Phase III. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4365767</comments>
            <pubDate>Wed, 19 Jan 2011 13:09:19 +0100</pubDate>
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            <title>GlaxoSmithKline commences Phase III study of intravenous zanamivir for hospitalised patients with influenza</title>
            <link>http://www.medworm.com/index.php?rid=4365768&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011_pressrelease_10015.htm</link>
            <description>GlaxoSmithKline (GSK) announced today that the first patient has received treatment in a pivotal Phase III study of hospitalised patients with influenza which compares intravenous (IV) zanamivir to oral oseltamivir. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4365768</comments>
            <pubDate>Wed, 19 Jan 2011 09:00:19 +0100</pubDate>
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            <title>GlaxoSmithKline announces Q4 2010 legal charge</title>
            <link>http://www.medworm.com/index.php?rid=4357812&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011_pressrelease_10014.htm</link>
            <description>GlaxoSmithKline (GSK) today announces that it expects to record a legal charge for the fourth quarter of 2010 of £2.2 billion ($3.4 billion) (equating to an after tax cost of £1.8 billion). (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4357812</comments>
            <pubDate>Mon, 17 Jan 2011 14:58:30 +0100</pubDate>
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            <title>GlaxoSmithKline and ChemoCentryx announce initiation of Phase III study of GSK’786, formerly Traficet-EN™, for the treatment of Crohn’s disease</title>
            <link>http://www.medworm.com/index.php?rid=4334069&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011_pressrelease_10013.htm</link>
            <description>GlaxoSmithKline (GSK) and ChemoCentryx, Inc. announced today that the first patient with Crohn’s disease has initiated treatment in the initial pivotal induction study comparing Traficet-EN, now designated GSK1605786 (‘786), to placebo. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4334069</comments>
            <pubDate>Wed, 12 Jan 2011 13:00:00 +0100</pubDate>
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            <title>GSK phase III study in HER2-positive advanced breast cancer shows an overall survival benefit when Tyk(v)erb is combined with Paclitaxel</title>
            <link>http://www.medworm.com/index.php?rid=4391230&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2FLibrary%2Fmedia%2Fpressreleases%2F2011_pressrelease_138370.htm</link>
            <description>In a blinded, randomized, Phase III study, women with an advanced form of breast cancer achieved a statistically-significant improvement in overall survival when treated with an investigational combination of Tyk(v)erb® (lapatinib) plus paclitaxel, a widely used chemotherapy agent.[i] The results of the Phase III study in HER2-positve metastatic breast cancer were presented during the 33rd annual meeting of the CTRC-AACR San Antonio Breast Cancer Symposium, held in San Antonio, Texas (Dec. 8 – 12). (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4391230</comments>
            <pubDate>Mon, 10 Jan 2011 19:40:00 +0100</pubDate>
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            <title>Avodart reviewed by FDA advisory committee for prostate cancer risk reduction</title>
            <link>http://www.medworm.com/index.php?rid=4391231&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2FLibrary%2Fmedia%2Fpressreleases%2F2011_pressrelease_137614.htm</link>
            <description>GlaxoSmithKline today announced the results of a U.S. Food and Drug Administration (FDA) Oncologic Drugs Advisory Committee (ODAC) meeting to discuss the supplemental New Drug Application (sNDA) for Avodart® (dutasteride) for reducing the risk of prostate cancer in men at risk for the disease, defined as those who have had a prior negative biopsy due to clinical concern and have an elevated serum prostate-specific antigen (PSA). When asked if the dutasteride risk/benefit profile is favorable for reduction in the risk of prostate cancer in this target population, the ODAC voted 14 against, 2 in favor, and 2 abstentions. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4391231</comments>
            <pubDate>Mon, 10 Jan 2011 00:00:00 +0100</pubDate>
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        <item>
            <title>GlaxoSmithKline and DENTSPLY International sign global agreement to create a portfolio of co-branded professional oral care products</title>
            <link>http://www.medworm.com/index.php?rid=4328254&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2011_pressrelease_10012.htm</link>
            <description>GlaxoSmithKline (GSK) and DENTSPLY International, a global leader in professional dental products, today announced that they have entered into an agreement to create a portfolio of co-branded oral care products to be used in the dental office by patients suffering from tooth sensitivity, a problem which is estimated to affect 1 in 3 people. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4328254</comments>
            <pubDate>Fri, 07 Jan 2011 18:58:35 +0100</pubDate>
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        <item>
            <title>GSK and Theravance announce progression of LAMA/LABA combination treatment into Phase III development for COPD</title>
            <link>http://www.medworm.com/index.php?rid=4430547&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2FLibrary%2Fmedia%2Fpressreleases%2F2011_pressrelease_10022.htm</link>
            <description>Relovair™ programme expanded by start of large Phase IIIb COPD outcomes study (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4430547</comments>
            <pubDate>Thu, 06 Jan 2011 12:00:00 +0100</pubDate>
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        <item>
            <title>GSK phase III study in HER2-positive advanced breast cancer shows an overall survival benefit when Tyk(v)erb is combined with Paclitaxel</title>
            <link>http://www.medworm.com/index.php?rid=4391232&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2FLibrary%2Fmedia%2Fpressreleases%2F2011_pressrelease_137605.htm</link>
            <description>In a blinded, randomized, Phase III study, women with an advanced form of breast cancer achieved a statistically-significant improvement in overall survival when treated with an investigational combination of Tyk(v)erb® (lapatinib) plus paclitaxel, a widely used chemotherapy agent. The results of the Phase III study in HER2-positve metastatic breast cancer were presented during the 33rd annual meeting of the CTRC-AACR San Antonio Breast Cancer Symposium, held in San Antonio, Texas (Dec. 8 – 12). (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4391232</comments>
            <pubDate>Tue, 04 Jan 2011 00:00:00 +0100</pubDate>
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        <item>
            <title>GSK responds to 60 Minutes</title>
            <link>http://www.medworm.com/index.php?rid=4328255&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2011%2F2010_us_pressrelease_10111.htm</link>
            <description>GlaxoSmithKline [GSK] issued the following response regarding a 60 Minutes program on January 2 that focused on a manufacturing facility in Puerto Rico which was formerly owned by the company. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4328255</comments>
            <pubDate>Mon, 03 Jan 2011 02:29:01 +0100</pubDate>
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        <item>
            <title>GlaxoSmithKline and Theravance commence MABA Phase IIb COPD study</title>
            <link>http://www.medworm.com/index.php?rid=4328256&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_us_pressrelease_10108.htm</link>
            <description>GlaxoSmithKline (GSK) and Theravance (NASDAQ: THRX) announced today that the first patient has started treatment with an investigational inhaledbifunctional compound GSK961081 (‘081) in a Phase IIb study to evaluate efficacy and safety in patients with moderate to severe chronic obstructive pulmonary disease (COPD). (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4328256</comments>
            <pubDate>Tue, 21 Dec 2010 21:00:23 +0100</pubDate>
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        <item>
            <title>Andrew Witty appointed Lead Non-Executive Board Member for the Department for Business, Innovation and Skills (BIS)</title>
            <link>http://www.medworm.com/index.php?rid=4261855&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10130.htm</link>
            <description>The UK Government today announced that Andrew Witty has been appointed as the Lead Non-Executive Board Member for the Department for Business, Innovation and Skills. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4261855</comments>
            <pubDate>Thu, 16 Dec 2010 01:00:00 +0100</pubDate>
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        <item>
            <title>GSK to strengthen Nutritional Healthcare business with acquisition of Maxinutrition</title>
            <link>http://www.medworm.com/index.php?rid=4255796&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10128.htm</link>
            <description>GSK’ and Maxinutrition Group Holdings Limited today announced they have entered into an agreement for GSK to acquire Maxinutrition, a UK company that manufactures protein-enhanced functional nutrition products, from Darwin Private Equity. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4255796</comments>
            <pubDate>Mon, 13 Dec 2010 11:00:00 +0100</pubDate>
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            <title>Data from Tykerb investigational phase III studies in neo-adjuvant HER2-positive breast cancer presented at breast cancer symposium</title>
            <link>http://www.medworm.com/index.php?rid=4247540&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10127.htm</link>
            <description>Topline results were presented today from two Phase III studies examining the effect of Tykerb (lapatinib) in the neo-adjuvant setting of HER2-positive breast cancer.i, ii The combination of lapatinib and trastuzumab, with standard chemotherapy, was compared to standard chemotherapy plus either lapatinib or trastuzumab in a trial called NeoALTTO. In another trial, known as GeparQuinto, lapatinib plus standard chemotherapy was compared to trastuzumab plus standard chemotherapy. The studies were conducted and presented by international cooperative groups, with research being funded in part by GlaxoSmithKline. Data findings from both trials were presented at the 33rd annual meeting of the CTRC-AACR San Antonio Breast Cancer Symposium (SABCS), held in San Antonio, Texas (8-12 December 2010). (...</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4247540</comments>
            <pubDate>Fri, 10 Dec 2010 15:36:00 +0100</pubDate>
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        <item>
            <title>GSK signs agreement to acquire Nanjing MeiRui Pharmaceuticals in China</title>
            <link>http://www.medworm.com/index.php?rid=4235351&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10126.htm</link>
            <description>GSK announced that it has entered into an agreement to acquire Nanjing MeiRui Pharma Co., Ltd (MeiRui) for a cash consideration of approximately $70 million. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4235351</comments>
            <pubDate>Tue, 07 Dec 2010 09:00:00 +0100</pubDate>
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            <title>GlaxoSmithKline and Human Genome Sciences announce FDA extension of Benlysta® PDUFA target date to 10th March 2011</title>
            <link>http://www.medworm.com/index.php?rid=4231755&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_us_pressrelease_10104.htm</link>
            <description>GSK and Human Genome Sciences announced that the US FDA has extended the PDUFA target date for its priority review of the BLA for Benlysta® (belimumab) as a potential treatment for systemic lupus erythematosus (SLE) from 9 December 2010 to 10 March 2011. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4231755</comments>
            <pubDate>Fri, 03 Dec 2010 22:00:00 +0100</pubDate>
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            <title>Government patent box proposals ‘transform’ UK attractiveness for investment</title>
            <link>http://www.medworm.com/index.php?rid=4210589&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10124.htm</link>
            <description>GSK welcomes the publication today of the Government’s proposals to establish a ‘patent box’. The measure is designed to encourage investment in RD and related manufacturing in the UK by introducing a lower rate of corporation tax on profits generated from UK-owned intellectual property. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4210589</comments>
            <pubDate>Mon, 29 Nov 2010 16:00:00 +0100</pubDate>
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            <title>GlaxoSmithKline to increase its shareholding in Theravance</title>
            <link>http://www.medworm.com/index.php?rid=4210590&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10123.htm</link>
            <description>GlaxoSmithKline plc (GSK) and Theravance, Inc. (NASDAQ: THRX) (the “Company”) announced today that GSK will increase its shareholding in Theravance through the purchase of Theravance common stock in a private placement. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4210590</comments>
            <pubDate>Mon, 29 Nov 2010 09:30:00 +0100</pubDate>
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        <item>
            <title>GlaxoSmithKline and JSC Binnopharm enter vaccine production alliance in Russia</title>
            <link>http://www.medworm.com/index.php?rid=4210591&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10122.htm</link>
            <description>GlaxoSmithKline (GSK) and JSC Binnopharm (Binnopharm) today announced an alliance to enable the local secondary manufacture of a number of GSK vaccines in Russia. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4210591</comments>
            <pubDate>Fri, 26 Nov 2010 10:30:00 +0100</pubDate>
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            <title>New study findings show no benefit of prescription omega-3 fatty acids in prevention of recurrent symptomatic atrial fibrillation in affected patients</title>
            <link>http://www.medworm.com/index.php?rid=4165689&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10120.htm</link>
            <description>Findings from a new study show, compared to placebo, treatment with high-dose prescription omega-3 fatty acids did not reduce the recurrence of symptomatic atrial fibrillation (AF) among patients with symptomatic paroxysmal AF or persistent AF who have no evidence of substantial structural heart disease. The study was presented today at the American Heart Association’s Scientific Sessions and also published online in The Journal of the American Medical Association. (Source: GSK news)</description>
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            <pubDate>Mon, 15 Nov 2010 14:00:00 +0100</pubDate>
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            <title>GlaxoSmithKline and Fiocruz extend innovative collaboration to research and develop new medicines for neglected tropical diseases</title>
            <link>http://www.medworm.com/index.php?rid=4161026&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10119.htm</link>
            <description>GlaxoSmithKline and the Oswald Cruz Foundation (Fiocruz) have today announced a unique collaboration to research and develop new and innovative medicines to treat diseases which disproportionately affect people living in the world’s poorest countries. (Source: GSK news)</description>
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            <pubDate>Fri, 12 Nov 2010 14:30:00 +0100</pubDate>
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            <title>GSK and Amicus Therapeutics enter exclusive worldwide agreement to develop and commercialise Amigal™ for Fabry disease</title>
            <link>http://www.medworm.com/index.php?rid=4113398&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10118.htm</link>
            <description>Amicus to receive $60m in upfront license payment and equity investment and eligible for approximately $170M million in future potential milestone payments (Source: GSK news)</description>
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            <pubDate>Fri, 29 Oct 2010 11:30:00 +0100</pubDate>
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            <title>GlaxoSmithKline receives approval in Japan for two medicines: Revolade and Xyzal</title>
            <link>http://www.medworm.com/index.php?rid=4113399&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10117.htm</link>
            <description>GlaxoSmithKline (GSK) announced that it has received approval in Japan from the Ministry of Health, Labour and Welfare for Revolade (eltrombopag) for the treatment of the blood disorder, chronic idiopathic thrombocytopenic purpura (ITP), and for Xyzal (levocetirizine dihydrochloride), the first new anti-histamine to be made available in Japan for eight years. (Source: GSK news)</description>
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            <pubDate>Fri, 29 Oct 2010 11:00:00 +0100</pubDate>
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            <title>GSK announces Q3 results for 2010</title>
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            <description>Q3 EPS before major restructuring of 28.2p. Q3 dividend up 7% to 16p. (Source: GSK news)</description>
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            <pubDate>Thu, 21 Oct 2010 11:00:00 +0100</pubDate>
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            <title>GSK outlines approach to delivering advances in the treatment of rare diseases</title>
            <link>http://www.medworm.com/index.php?rid=4079896&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10114.htm</link>
            <description>GlaxoSmithKline (GSK) today provided further details about the strategic focus and development priorities of the company’s unit dedicated to rare diseases, which was launched in February 2010. (Source: GSK news)</description>
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            <pubDate>Mon, 18 Oct 2010 13:00:00 +0100</pubDate>
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            <title>GSK, Fondazione Telethon and Fondazione San Raffaele to collaborate on gene therapy for rare diseases</title>
            <link>http://www.medworm.com/index.php?rid=4075931&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10113.htm</link>
            <description>GlaxoSmithKline PLC (GSK), Fondazione Telethon and Fondazione San Raffaele today announced a new strategic alliance to research and develop novel treatments to address rare genetic disorders, using gene therapy carried out on stem cells taken from the patient’s bone marrow (ex vivo). The alliance capitalises on research performed at the San Raffaele Telethon Institute for Gene Therapy (HSR-TIGET), a joint venture between Fondazione Telethon and Fondazione San Raffaele established since 1995. (Source: GSK news)</description>
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            <pubDate>Mon, 18 Oct 2010 11:00:00 +0100</pubDate>
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            <title>GSK increases support for WHO strategy to improve children’s health with new 5-year commitment to expand donations of albendazole medicine</title>
            <link>http://www.medworm.com/index.php?rid=4070492&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10110.htm</link>
            <description>At the launch of the World Health Organization’s (WHO) first report on Neglected Tropical Diseases today, GSK announced a new five year commitment to expand the donation of its medicine albendazole to treat children at risk of intestinal worms, known as soil-transmitted helminths (STH). (Source: GSK news)</description>
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            <pubDate>Thu, 14 Oct 2010 09:00:00 +0100</pubDate>
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            <title>GSK provides update on Herpevac trial for women evaluating Simplirix™ (Herpes Simplex Vaccine)</title>
            <link>http://www.medworm.com/index.php?rid=4016021&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10105.htm</link>
            <description>GlaxoSmithKline (GSK) has made the decision not to pursue further worldwide development of Simplirix™ (Herpes Simplex Vaccine), an experimental vaccine intended to prevent genital herpes disease in women. (Source: GSK news)</description>
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            <pubDate>Thu, 30 Sep 2010 14:00:00 +0100</pubDate>
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            <title>GlaxoSmithKline receives EU approval for a new therapeutic indication for Arixtra® (fondaparinux)</title>
            <link>http://www.medworm.com/index.php?rid=4008400&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10104.htm</link>
            <description>GlaxoSmithKline (GSK) confirmed today that the European Commission (EC) has granted an amendment of their marketing authorisation for their anti-clotting agent (antithrombotic) Arixtra® (fondaparinux) in the European Union for a new therapeutic indication. (Source: GSK news)</description>
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            <pubDate>Wed, 29 Sep 2010 09:00:00 +0100</pubDate>
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            <title>GSK regulatory update on Avandia following EMA and FDA reviews</title>
            <link>http://www.medworm.com/index.php?rid=3996375&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10103.htm</link>
            <description>GSK confirms that following a review of Avandia® by the EMA and the US FDA, each agency has today announced their individual regulatory decisions and the resulting actions. (Source: GSK news)</description>
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            <pubDate>Thu, 23 Sep 2010 16:30:00 +0100</pubDate>
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            <title>GSK EU regulatory update on Pandemrix™</title>
            <link>http://www.medworm.com/index.php?rid=3996376&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fus.gsk.com%2Fhtml%2Fmedia-news%2Fpressreleases%2F2010%2F2010_pressrelease_10102.htm</link>
            <description>GSK confirmed that on behalf of the EMA, the CHMP has concluded that the available data are insufficient to demonstrate a causal relationship between Pandemrix and the observed cases of narcolepsy. (Source: GSK news)</description>
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            <pubDate>Thu, 23 Sep 2010 16:00:00 +0100</pubDate>
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            <title>GSK and Theravance announce combination ICS/LABA Phase II results in the Relovair™ development programme</title>
            <link>http://www.medworm.com/index.php?rid=3990607&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10101.htm</link>
            <description>Additional data presentations for fluticasone furoate and vilanterol trifenatate support the potential of developmental combination treatment, Relovair, in COPD and asthma (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Wed, 22 Sep 2010 12:00:00 +0100</pubDate>
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            <title>GlaxoSmithKline and Genmab refocus development programme for ofatumumab in autoimmune indications</title>
            <link>http://www.medworm.com/index.php?rid=3974953&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10098.htm</link>
            <description>Following the 1st July announcement by GlaxoSmithKline (GSK) and Genmab A/S (OMX: GEN) of an amendment to the collaborative agreement for ofatumumab in which GSK assumed development responsibility for autoimmune indications, GSK and Genmab announced today plans to refocus the development programme of ofatumumab in autoimmune indications. (Source: GSK news)</description>
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            <pubDate>Thu, 16 Sep 2010 08:00:00 +0100</pubDate>
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            <title>GSK and BJD collaborate on a new educational programme to reduce global burden of joint pain</title>
            <link>http://www.medworm.com/index.php?rid=3963882&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10097.htm</link>
            <description>The Bone and Joint Decade (BJD) international initiative and GlaxoSmithKline (GSK) today announced the launch of the LIBERATE™ joint pain management programme during the BJD’s World Conference in Lund, Sweden. (Source: GSK news)</description>
            <author>GSK news</author>
            <type>news</type>
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            <pubDate>Sat, 11 Sep 2010 10:00:00 +0100</pubDate>
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            <title>GlaxoSmithKline and Genmab announce start of ofatumumab Phase III combination study in non-Hodgkin’s lymphoma</title>
            <link>http://www.medworm.com/index.php?rid=3963883&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10096.htm</link>
            <description>GlaxoSmithKline (GSK) and Genmab A/S (OMX: GEN) announced today the start of a Phase III study in patients with indolent B-cell non-Hodgkin’s lymphoma (B-NHL) who did not respond to or progressed during, or within 6 months of a rituximab containing regimen. (Source: GSK news)</description>
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            <pubDate>Wed, 08 Sep 2010 18:00:00 +0100</pubDate>
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            <title>GSK announces succession plan for Chief Financial Officer</title>
            <link>http://www.medworm.com/index.php?rid=3944676&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10094.htm</link>
            <description>GlaxoSmithKline plc (GSK) today announces that Julian Heslop is to retire as Chief Financial Officer and Executive Director of the company at the end of March 2011. He will be succeeded by Simon Dingemans who is appointed Chief Financial Officer designate and Executive Director effective 4th January 2011. (Source: GSK news)</description>
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            <pubDate>Wed, 08 Sep 2010 13:00:00 +0100</pubDate>
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            <title>GSK signs agreement with Lonza to secure capacity and expertise in biological manufacturing to support ongoing development of GSK’s biopharmaceuticals portfolio</title>
            <link>http://www.medworm.com/index.php?rid=3944678&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10092.htm</link>
            <description>GlaxoSmithKline (GSK) and Lonza today announced that they have entered into a new agreement under which Lonza will support the ongoing development of GSK’s biopharmaceutical pipeline by supplying manufacturing capacity for five early stage monoclonal antibodies. (Source: GSK news)</description>
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            <pubDate>Wed, 08 Sep 2010 08:00:00 +0100</pubDate>
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            <title>Galapagos reaches agreement to acquire GlaxoSmithKline research centre in Zagreb, Croatia</title>
            <link>http://www.medworm.com/index.php?rid=3944677&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10091.htm</link>
            <description>Galapagos and GlaxoSmithKline today announced they have reached an agreement for Galapagos to acquire GSK’s state-of-the art research centre in Zagreb, Croatia. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Wed, 08 Sep 2010 08:00:00 +0100</pubDate>
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            <title>BBC Panorama – 6 September 2010: “A Risk Worth Taking?” Programme. GlaxoSmithKline Right of Reply Statement</title>
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            <description>(Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Mon, 06 Sep 2010 19:30:00 +0100</pubDate>
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            <title>GlaxoSmithKline pre-broadcast statement: BBC Panorama, 6 September 2010</title>
            <link>http://www.medworm.com/index.php?rid=3937618&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10089.htm</link>
            <description>GlaxoSmithKline today issued the following statement in anticipation of the BBC Panorama programme, 'A risk worth taking?' which is scheduled to be aired this evening. (Source: GSK news)</description>
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            <pubDate>Mon, 06 Sep 2010 10:00:00 +0100</pubDate>
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            <title>GlaxoSmithKline responds to British Medical Journal article regarding Avandia® (rosiglitazone)</title>
            <link>http://www.medworm.com/index.php?rid=3937619&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10088.htm</link>
            <description>GlaxoSmithKline (GSK) continues to work in the best interest of diabetes patients who face this chronic and serious disease. Patients taking Avandia should speak with their doctor about their treatment and any questions they may have regarding their medicine. (Source: GSK news)</description>
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            <pubDate>Mon, 06 Sep 2010 00:01:00 +0100</pubDate>
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            <title>Reports of narcolepsy in Europe following vaccination with Pandemrix™</title>
            <link>http://www.medworm.com/index.php?rid=3931384&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10087.htm</link>
            <description>GSK initially became aware of possible cases of narcolepsy following vaccination with the adjuvanted H1N1 pandemic vaccine Pandemrix through adverse event reports received by the Swedish Medical Products Agency, and subsequently via media reports in Finland. (Source: GSK news)</description>
            <author>GSK news</author>
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            <pubDate>Thu, 02 Sep 2010 17:00:00 +0100</pubDate>
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            <title>GSK and Valeant announce new US FDA PDUFA goal date for ezogabine</title>
            <link>http://www.medworm.com/index.php?rid=3931385&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_us_pressrelease_10072.htm</link>
            <description>GlaxoSmithKline (NYSE: GSK) and Valeant Pharmaceuticals International (NYSE: VRX) announced today the U.S. Food and Drug Administration (FDA) has extended the Prescription Drug User Fee Act (PDUFA) goal date for ezogabine to 30 November 2010. (Source: GSK news)</description>
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            <pubDate>Mon, 30 Aug 2010 18:00:00 +0100</pubDate>
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            <title>GSK European Commission amends licence for Cervarix®</title>
            <link>http://www.medworm.com/index.php?rid=3897926&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10085.htm</link>
            <description>GlaxoSmithKline (GSK) confirmed today that the European Commission has granted Marketing Authorisation to amend the licence for its cervical cancer vaccine, Cervarix®. (Source: GSK news)</description>
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            <pubDate>Tue, 24 Aug 2010 10:00:00 +0100</pubDate>
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            <title>GSK commences Phase III clinical trials to develop herpes zoster vaccine for the prevention of shingles</title>
            <link>http://www.medworm.com/index.php?rid=3893962&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10084.htm</link>
            <description>GlaxoSmithKline confirmed that the company has commenced the Phase III clinical trials programme of its candidate herpes zoster vaccine currently being developed for the prevention of shingles. (Source: GSK news)</description>
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            <pubDate>Mon, 23 Aug 2010 10:00:00 +0100</pubDate>
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            <title>GlaxoSmithKline and Human Genome Sciences announce FDA priority review designation for Benlysta® (belimumab) as a potential treatment for systemic lupus erythematosus</title>
            <link>http://www.medworm.com/index.php?rid=3883701&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10083.htm</link>
            <description>GlaxoSmithKline PLC (GSK) and Human Genome Sciences, Inc. today announced that the U.S. Food and Drug Administration (FDA) has granted a priority review designation to Benlysta® (belimumab) as a potential treatment for systemic lupus erythematosus (SLE). A priority review designation is granted to drugs that, if approved, offer major advances in treatment or provide a treatment where no adequate therapy exists. The FDA has assigned belimumab a Prescription Drug User Fee Act (PDUFA) target date of 9 December 2010. (Source: GSK news)</description>
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            <pubDate>Thu, 19 Aug 2010 11:30:00 +0100</pubDate>
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            <title>GSK and Genmab announce topline results from the concluded pivotal trial of Arzerra (ofatumumab) in fludarabine and alemtuzumab refractory chronic lymphocytic leukemia</title>
            <link>http://www.medworm.com/index.php?rid=3847274&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10082.htm</link>
            <description>GlaxoSmithKline (GSK) and Genmab A/S (OMX: GEN) announced today top line results from the concluded pivotal trial of ofatumumab in patients with fludarabine and alemtuzumab refractory chronic lymphocytic leukemia (CLL). (Source: GSK news)</description>
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            <pubDate>Mon, 09 Aug 2010 20:00:00 +0100</pubDate>
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            <title>Image of new antibiotic in action opens up new opportunities to combat antibacterial resistance</title>
            <link>http://www.medworm.com/index.php?rid=3825670&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10080.htm</link>
            <description>Detailed pictures have been published today showing how a new type of experimental antibiotic can kill bacteria already resistant to existing treatments. The findings could ultimately help scientists to develop new antibiotics to tackle the bacteria responsible for many hospital and community-acquired infections. (Source: GSK news)</description>
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            <pubDate>Thu, 05 Aug 2010 08:30:00 +0100</pubDate>
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            <title>GSK exercises option on Anacor's novel antibiotic for the treatment of gram-negative infections</title>
            <link>http://www.medworm.com/index.php?rid=3825671&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10081.htm</link>
            <description>GlaxoSmithKline PLC (GSK) and Anacor Pharmaceuticals today announced that GSK has exercised its option to obtain an exclusive licence to develop and commercialise GSK2251052 (GSK '052), formerly known as AN3365. GSK '052 is a novel, systemic antibiotic derived from Anacor's boron chemistry platform. (Source: GSK news)</description>
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            <pubDate>Thu, 29 Jul 2010 11:00:00 +0100</pubDate>
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            <title>GSK receives CHMP positive opinion for a new indication for Arixtra</title>
            <link>http://www.medworm.com/index.php?rid=3782620&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10079.htm</link>
            <description>The first treatment available for superficial vein thrombosis in Europe (Source: GSK news)</description>
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            <pubDate>Fri, 23 Jul 2010 11:30:00 +0100</pubDate>
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            <title>GlaxoSmithKline statement in response to FDA announcement on TIDE trial</title>
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            <description>GlaxoSmithKline [NYSE: GSK] confirmed today that it will suspend enrollment of new patients in the Thiazolidinedione Intervention with Vitamin D Evaluation (TIDE) clinical trial at the request of the U.S. Food and Drug Administration (FDA) pending FDA review of recommendations from its Advisory Committee meeting July 13-14. (Source: GSK news)</description>
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            <pubDate>Wed, 21 Jul 2010 16:15:00 +0100</pubDate>
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            <description>Q2 EPS before major restructuring 2.6p (29.3p excluding pre-announced legal charge) (Source: GSK news)</description>
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            <pubDate>Wed, 21 Jul 2010 12:00:00 +0100</pubDate>
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            <description>GlaxoSmithKline (GSK) today announces that it expects to record a legal charge for the second quarter of 2010 of £1.57billion ($2.36 billion) (equating to an after tax cost of £1.35 billion).  The charge includes settlements, agreements in principle to settle, and other provisioning for long-standing legal cases. (Source: GSK news)</description>
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            <pubDate>Thu, 15 Jul 2010 06:00:00 +0100</pubDate>
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            <title>GlaxoSmithKline statement in response to FDA Advisory Committees’ vote on safety of Avandia® (rosiglitazone)</title>
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            <description>GlaxoSmithKline [NYSE: GSK] confirmed today that a joint advisory committee to the U.S. Food and Drug Administration (FDA) voted to allow Avandia to remain on the market. (Source: GSK news)</description>
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            <pubDate>Wed, 14 Jul 2010 21:15:00 +0100</pubDate>
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            <title>GlaxoSmithKline (GSK) responds to Senate Finance Committee letter of 12 July to FDA</title>
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            <description>. (Source: GSK news)</description>
            <author>GSK news</author>
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            <title>Data support Avandia (rosiglitazone maleate) cardiovascular safety profile</title>
            <link>http://www.medworm.com/index.php?rid=3739175&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10074.htm</link>
            <description>The U.S. Food and Drug Administration (FDA) today posted a comprehensive review conducted by GlaxoSmithKline (GSK) of the cardiovascular safety data on Avandia® (rosiglitazone maleate). GSK’s review supports the overall positive benefit-risk profile of rosiglitazone as an important medicine for patients with type 2 diabetes. (Source: GSK news)</description>
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            <pubDate>Fri, 09 Jul 2010 13:30:00 +0100</pubDate>
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            <title>GSK EU regulatory update on Avandia (rosiglitazone)</title>
            <link>http://www.medworm.com/index.php?rid=3739176&amp;cid=s_37964_34_f&amp;fid=37964&amp;url=http%3A%2F%2Fwww.gsk.com%2Fmedia%2Fpressreleases%2F2010%2F2010_pressrelease_10072.htm</link>
            <description>GlaxoSmithKline (GSK) today confirmed that on behalf of the European Medicines Agency (EMA), the Committee for Medicinal Products for Human Use (CHMP) is to review the benefit/risk profile of Avandia (rosiglitazone). (Source: GSK news)</description>
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            <pubDate>Fri, 09 Jul 2010 09:00:00 +0100</pubDate>
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            <title>GSK and EDB commit $35 million (USD) in funding to support research in green and sustainable manufacturing in Singapore</title>
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            <description>GlaxoSmithKline (GSK) and the Singapore Economic Development Board (EDB), the government agency responsible for economic growth and development, today jointly awarded funding for eight research projects based in Singapore aimed at growing local capabilities and talent in green and sustainable manufacturing. (Source: GSK news)</description>
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            <pubDate>Fri, 02 Jul 2010 11:00:00 +0100</pubDate>
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            <title>GlaxoSmithKline and Genmab announce amendment to Ofatumumab agreement</title>
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            <description>GlaxoSmithKline (GSK) and Genmab A/S (OMX: GEN) announced today an amendment to the ofatumumab co-development and commercialisation agreement. (Source: GSK news)</description>
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            <pubDate>Thu, 01 Jul 2010 16:00:00 +0100</pubDate>
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