Updated Pfizer Pipeline Focuses on Value, Unmet Medical Need
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- Category: Pfizer
Pfizer Inc. (NYSE: PFE) provided an update to its development pipeline, which includes 118 programs from Phase 1 through registration. The updated pipeline continues to reflect Pfizer's ongoing investment in high-priority disease areas with considerable unmet medical need.
Novartis sells US rights to the overactive bladder treatment Enablex®
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- Category: Novartis
Novartis has signed an agreement to sell to Warner Chilcott plc the US rights to market Enablex®* (darifenacin) extended release tablets, a medicine to treat adults with symptoms of overactive bladder. The agreement will be filed with the US Federal Trade Commission under the Hart-Scott-Rodino Act and, subject to certain closing conditions set forth in the agreement, the transaction is expected to close by the end of October 2010.
GSK regulatory update on Avandia following EMA and FDA reviews
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- Category: GlaxoSmithKline
GlaxoSmithKline (GSK) confirms that following a review of Avandia® (rosiglitazone maleate) by the European Medicines Agency (EMA) and the US Food and Drug Administration (FDA), each agency has announced their individual regulatory decisions and the resulting actions.
Merck KGaA Announces CHMP Opinion for Cladribine Tablets in Multiple Sclerosis
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- Category: Merck Group
Merck KGaA announced today that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has issued a negative opinion regarding the marketing authorization application (MAA) for Cladribine Tablets as a treatment for relapsing-remitting multiple sclerosis (MS).
Abbott's XIENCE V(R) Shows Continued Strong Performance
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- Category: Abbott
Late-breaking data were presented from the investigator-initiated COMPARE trial of 1,800 real-world patients involving Abbott's (NYSE: ABT) market-leading XIENCE V(R) Everolimus Eluting Coronary Stent System and the TAXUS(R) Liberte(R) Paclitaxel-Eluting Coronary Stent System (TAXUS).
Novartis gains FDA approval for Gilenya(TM), a novel first-line multiple sclerosis treatment
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- Category: Novartis
Novartis announced that the US Food and Drug Administration (FDA) approved the oral multiple sclerosis (MS) treatment Gilenya(TM) (fingolimod) 0.5 mg daily, a first-line treatment for relapsing forms of multiple sclerosis - the most common forms of the disease. The FDA approval makes Gilenya the first oral treatment indicated for relapsing forms of MS available in the US.
Amgen and Pfizer Introduce 'Psophisticated Style: A Guide to Everyday Style and Psoriasis(TM)'
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- Category: Amgen
Amgen and Pfizer announced the launch of "Psophisticated Style: A Guide to Everyday Style and Psoriasis(TM)", an online resource, providing a wealth of style advice specifically for people with psoriasis. Hosted by Tim Gunn, mentor to the designers on TV's "Project Runway" and chief creative officer of Liz Claiborne, Inc. and dermatologist Susan C. Taylor, M.D., the style guide includes five videos, which illustrate various style issues for individuals with psoriasis.
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