Pfizer reports top-line results of study of Lyrica's effect on male reproduction
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- Category: Pfizer
Pfizer Inc. (NYSE: PFE) announced today that top-line results for Lyrica® (pregabalin) capsules CV Study A0081104 - Assessment of the Impact of Lyrica on Sperm Production in Healthy Volunteers - demonstrate that Lyrica does not affect the reproductive function in healthy males when compared to placebo.
Novartis gains FDA approval for Afinitor® in advanced breast cancer
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- Category: Novartis
The US Food and Drug Administration (FDA) has approved Afinitor® (everolimus) tablets* (approval represents the first major advance for US patients with advanced HR+ breast cancer since aromatase inhibitors were introduced more than 15 years ago[1])
Novartis second quarter results enhance future growth prospects
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- Category: Novartis
Group net sales reached USD 14.3 billion (-4%, +1% cc) in the second quarter, with growth from recently launched products more than offsetting the loss associated with the Diovan patent expiration.
Abbott reports second quarter results
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- Category: Abbott
Abbott (NYSE: ABT) announced financial results for the second quarter ended June 30, 2012. Diluted earnings per share, excluding specified items, were $1.23, reflecting 9.8 percent growth, exceeding Abbott's guidance range.
AstraZeneca to initiate a new study of BRILINTA (Ticagrelor) in patients with PAD
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- Category: AstraZeneca
AstraZeneca (NYSE: AZN) announced plans to conduct the EUCLID study, a global clinical trial involving 11,500 patients with peripheral artery disease (PAD), a condition affecting approximately 27 million people in Europe and North America.
GSK to acquire Human Genome Sciences for US$14.25 per share in cash
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- Category: GlaxoSmithKline
GlaxoSmithKline plc (LSE: GSK) and Human Genome Sciences (NASDAQ: HGSI) have entered into a definitive agreement under which GSK will acquire HGS for US$14.25 per share in cash. The transaction values HGS at approximately US$3.6 billion on an equity basis, or approximately US$3 billion net of cash and debt,
GSK and Theravance announce regulatory submissions for FF/VI
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- Category: GlaxoSmithKline
GlaxoSmithKline plc (GSK) and Theravance, Inc. (NASDAQ: THRX) announced the submission of regulatory applications in the US and European Union for the once-daily investigational medicine fluticasone furoate "FF"/vilanterol "VI" (FF/VI) for patients with chronic obstructive pulmonary disease (COPD) and a regulatory application for asthma in the European Union.
More Pharma News ...
- Boehringer Ingelheim pursuing health care innovation
- Abbott introduces OneLab, a novel integrated web-based software platform
- Boehringer Ingelheim establishes translational research collaboration with Harvard University
- Seven pharmaceutical companies join academic researchers to speed TB drug discovery
- Bristol-Myers Squibb and AstraZeneca expand diabetes alliance
- FDA grants priority review to the new drug application for Bayer's Regorafenib
- Roche to streamline research and development activities