Bayer Schering Pharma Initiates Phase III Trial of Regorafenib
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- Category: Bayer
Bayer Schering Pharma AG, Germany, has started to enroll patients in an international Phase III trial to evaluate its investigational compound regorafenib (BAY 73-4506) for the treatment of patients with metastatic colorectal cancer (CRC) who have progressed after standard therapies.
Bayer Schering Pharma Initiates Phase III Trial of Regorafenib (BAY 73-4506)
- Details
- Category: Bayer
Bayer Schering Pharma AG, Germany, has started to enroll patients in an international Phase III trial to evaluate its investigational compound regorafenib (BAY 73-4506) for the treatment of patients with metastatic colorectal cancer (CRC) who have progressed after standard therapies.
Lundbeck delivers strong growth
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- Category: Lundbeck
H. Lundbeck A/S (Lundbeck) reports first quarter revenue of DKK 3,849 million growing 15% in constant exchange rates compared to the first quarter results of 2009. Profit from operations was DKK 1,254 million, an increase of 32% compared to the same period last year.
Boehringer Ingelheim and Micromet announce global collaboration for multiple myeloma BiTE antibody
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- Category: Boehringer Ingelheim
Boehringer Ingelheim and Micromet, Inc. (Nasdaq: MITI) have entered into a collaboration agreement for the research, development and commercialization of a new BiTE antibody for the treatment of multiple myeloma.
Bayer Schering Pharma and EndoCeutics Enter into a Global Agreement
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- Category: Bayer
Bayer Schering Pharma AG, Germany, has signed a global exclusive cooperation agreement with the Canadian company EndoCeutics, Inc. for the development and commercialization of Vaginorm, an intra-vaginal application of dehydroepiandrosterone (DHEA).
Merck Announces First-Quarter 2010 Financial Results
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- Category: Merck
Merck & Co., Inc. (NYSE: MRK) announced financial results for the first quarter of 2010. Worldwide sales for the first quarter of 2010 were $11.4 billion. Net income for the first quarter was $299 million. Foreign exchange for the quarter favorably affected global sales performance by 4 percent.
FDA approved VIMOVO for arthritis patients at risk of developing NSAID-associated gastric ulcers
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- Category: AstraZeneca
AstraZeneca and POZEN Inc. announced the US Food and Drug Administration (FDA) has approved VIMOVO (naproxen and esomeprazole magnesium) delayed-release tablets for the relief of signs and symptoms of osteoarthritis, rheumatoid arthritis, and ankylosing spondylitis, and to decrease the risk of developing gastric ulcers in patients at risk of developing NSAID-associated gastric ulcers.
More Pharma News ...
- Nycomed and Merck & Co., Inc., announce commercialization agreements for Daxas®
- Bristol-Myers Squibb Reports Strong Sales, Earnings Performance in First Quarter
- AstraZeneca's first quarter results reflect continued strong market performance
- Bayer achieves strong gains in sales and earnings
- Boehringer Ingelheim grows faster than the pharmaceutical market
- Despite Concern, Americans Aren't Protecting Themselves Against Diabetes
- Roche Group sustained its strong sales growth in the first three months of 2010