Comparative Analysis of Marketed Drugs in Major Indications

London, United Kingdom (PressExposure) July 20, 2011 -- A patent offers the patentee a monopoly of market exclusivity, and ensures returns on research investments in the absence of competition, therefore encouraging research into novel treatment options.

In dyslipidemia, Lipitor is the world's biggest selling statin drug, with revenue of $11,434m in 2009. It was approved by the US FDA (United States Food and Drug Administration) in 1996. More than half of the antidyslipidemic market is commanded by Lipitor, which is a gold standard therapy. On January 6, 2009, the US Patent and Trademark office reissued a patent to Lipitor that will expire in June 2011. Apotex and Teva are seeking US FDA approval to sell generic versions of Lipitor, and were sued by Pfizer in 2008.

Exelon is available as a capsule, liquid and a patch form. The Exelon patch was recently approved by the FDA in 2007, and will not be available in generic form until the patent expires (2014). In 2007, Watson Pharmaceuticals was given tentative approval for its ANDA (Abbreviated New Drug Application) by the US FDA, to manufacture generic Exelon. Novartis and Watson Pharmaceuticals came to an agreement over the Exelon patent litigation. According to the agreement, Watson will not commence marketing its generic equivalent product until sometime prior to the expiration of the patents covering Exelon.

Teva Pharmaceuticals has received US FDA approval for the company's ANDA, to market the generic version of Eisai's Aricept.

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The monopoly granted by a patent lasts for a limited period of time. Extensions provide opportunities for a major marketed product to revive its sales and growth in the midst of heavy generic competition. Extensions can be obtained in terms of additional indications for the drug, or new dosage forms of the drug.

Tracleer received approval from the European regulatory authorities for the reduction in the number of new digital ulcers in patients suffering from systemic sclerosis and ongoing digital ulcer disease. Additionally, a quadrisect, dispersible 32mg tablet formulation of Tracleer has been approved in the EU (European Union) for the treatment of PAH (Pulmonary Arterial Hypertension) in children aged from two years.

Remicade was first approved by the FDA for Crohn's disease in 1998. Following this approval and successful clinical trials for other indications, the drug received FDA approval for several other indications, including psoriasis, ulcerative colitis, psoriatic arthritis, RA (Rheumatoid Arthritis) and ankylosing spondylitis. Aricept went off-patent in 2010. In 2009, Eisai received approval for a new oral jelly formulation of

GBI Research, the leading business intelligence provider, has released its latest research, "Comparative Analysis of Marketed Drugs in Major Indications - Patent Cliff to Set Off Intense Price Competition in High Volume Markets", which provides insights regarding the comparative analysis of marketed drugs based on safety, efficacy, cost of therapy and total sales revenue. The report also delves deep into the descriptions of every marketed drug, discussing their safety, efficacy, cost of therapy and clinical studies.

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Press Release Submitted On: July 20, 2011 at 1:16 am
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