FDA approves Micardis® (telmisartan) as the first treatment in its class
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- Category: Boehringer Ingelheim
Boehringer Ingelheim announced that the US Food and Drug Administration (FDA) has approved a new indication for Micardis® (telmisartan) for the reduction of the risk of myocardial infarction (heart attack), stroke, or death from cardiovascular (CV) causes in patients 55 years of age or older at high risk of developing major CV events who are unable to take ACE inhibitors.
FDA Approves CRESTOR for Use in Pediatric Patients with Heterozygous Familial Hypercholesterolemia
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- Category: AstraZeneca
AstraZeneca announced the US Food and Drug Administration (FDA) approved CRESTOR (rosuvastatin calcium) for use in children ages 10-17 with heterozygous familial hypercholesterolemia (HeFH) when diet therapy fails to reduce elevated cholesterol. HeFH, a genetic disease, is characterized by high LDL cholesterol (the "bad" cholesterol) and increased risk of early cardiovascular disease.
Pfizer And Wyeth Become One: Working Together For A Healthier Worldâ¢
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- Category: Pfizer
Pfizer Inc (NYSE: PFE) today announced that it has combined operations with Wyeth following the closing of the acquisition yesterday. Pfizer is now a more diversified health care company, with product offerings in human, animal, and consumer health, including vaccines, biologics, small molecules and nutrition across the developed and emerging markets.
Pfizer Completes Acquisition Of Wyeth
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- Category: Pfizer
Pfizer (NYSE: PFE) and Wyeth (NYSE: WYE) announced that Pfizer has completed its acquisition of Wyeth following the receipt of regulatory approval from all government authorities required by the merger agreement and approval by Wyeth shareholders.
GlaxoSmithKline and Prosensa form alliance to fight Duchenne Muscular Dystrophy
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- Category: GlaxoSmithKline
GlaxoSmithKline (GSK) and Prosensa, the Dutch based biopharmaceutical company focusing on RNA modulating therapeutics, have entered into an exclusive worldwide collaboration for the development and commercialisation of RNA based therapeutics for Duchenne Muscular Dystrophy (DMD).
Pfizer Receives Clearance From The U.S. Federal Trade Commission And The Canadian Competition Bureau
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- Category: Pfizer
Pfizer Inc (NYSE:PFE) has announced that the U.S. Federal Trade Commission terminated the waiting period under the Hart-Scott-Rodino Antitrust Improvements Act of 1976, as amended, with respect to Pfizer's pending acquisition of Wyeth. In addition, Pfizer has received approval from the Canadian Competition Bureau for the pending acquisition.
Expert Panel Offers Three-Step Plan to Guide People Toward Recovery of Depression
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- Category: Eli Lilly and Company
A new survey of 2,001 adults living with depression revealed that despite being diagnosed for an average of 12 years, many unknowingly took actions that could have sabotaged their chances of getting well.(1)
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- GSK's Avodart® / tamsulosin combination showed benefits for men with prostate enlargement
- Onyx Pharmaceuticals to Acquire Proteolix, Inc.
- FDA Advisory Committee Recommends Approval of Pfizer's Selzentry
- Access to HIV medication
- GSK expands presence in China through strategic cooperation