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Therapy Sector - Other
EVENTS
01 January 1970
London, UK
01 January 1970
San Diego, US
01 January 1970
Providence, Rhode Island, and San Francisco, California
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Glenmark Pharmaceuticals is developing a TRPA1 receptor antagonist for pain and respiratory disorders. The Indian company joins at least four other firms including Hydra Biosciences, Abbott and Janssen that are known to be working in the same ...
Abbott 's TNF alpha-targeting antibody Humira (adalimumab) has been filed in Japan for the additional indication of juvenile idiopathic arthritis (JIA). The submission is for a subcutaneously injected 40mg/0.8ml prefilled syringe formulation and a ...
NICE, the health technology appraisal institute for England and Wales, has U-turned on previous draft recommendations on biologic treatments for rheumatoid arthritis (RA). Two pieces of final guidance published today now give patients access to more ...
Widening losses at Oxford BioMedica in the first half of 2010 were tempered by positive news on a number of the company's product development programmes. These included possibilities for accelerating clinical trials with ProSavin, the gene-based ...
A joint meeting on 20 August of two US FDA advisory committees put major roadblocks in the way of Jazz Pharmaceuticals' new drug application (NDA) to sell sodium oxybate as a treatment for fibromyalgia. The panel of outside experts on arthritis ...
 
Meda of Sweden is to acquire the US speciality pharma company Alaven Pharmaceutical to enhance its US marketing capabilities and expand its therapeutic focus to include both gastroenterology and ...
Continued problems with anti-obesity drugs, more measures designed to improve R&D efficiency, and the approval of first-in-class therapeutics such as Amgen's Prolia and Dendreon's Provenge: the first ...
GW Pharma has enjoyed recent success with its cannabinoid extract product Sativex (nabiximols), which is now approved in the UK and Spain as an add-on therapy for spasticity in multiple sclerosis, ...
 
Pfizer has reiterated its commitment to developing an orphan and rare diseases franchise by acquiring the private US company FoldRx Pharmaceuticals. The two companies did not disclose the financial ...
Widening losses at Oxford BioMedica in the first half of 2010 were tempered by positive news on a number of the company's product development programmes. These included possibilities for accelerating ...
Baxter is to pay the Israeli biopharmaceutical company Kamada $20 million upfront for the commercial rights to its liquid alpha 1 -proteinase inhibitor Glassia in the US, Australia, New Zealand and ...
 
Abbott 's TNF alpha-targeting antibody Humira (adalimumab) has been filed in Japan for the additional indication of juvenile idiopathic arthritis (JIA). The submission is for a subcutaneously ...
Continued problems with anti-obesity drugs, more measures designed to improve R&D efficiency, and the approval of first-in-class therapeutics such as Amgen's Prolia and Dendreon's Provenge: the first ...
Novartis is to pay $10 million for the option to obtain the global licence to develop and commercialise Quark Pharmaceuticals' p53 temporary inhibitor small interfering RNA (siRNA) drug QPI-1002. The ...
 
Glenmark Pharmaceuticals is developing a TRPA1 receptor antagonist for pain and respiratory disorders. The Indian company joins at least four other firms including Hydra Biosciences, Abbott and ...
Widening losses at Oxford BioMedica in the first half of 2010 were tempered by positive news on a number of the company's product development programmes. These included possibilities for accelerating ...
Continued problems with anti-obesity drugs, more measures designed to improve R&D efficiency, and the approval of first-in-class therapeutics such as Amgen's Prolia and Dendreon's Provenge: the first ...
 
The treatment of rare diseases in Europe has been significantly enhanced by the EU's Orphan Drug Regulation and by raised levels of public awareness, thanks largely to the activities of interest ...
Rockwell Medical has met the US FDA to determine the Phase III trial design for its lead product, soluble ferric pyrophosphate (SFP), a continuous iron-replacement therapy for iron deficiency anaemia ...
Top-line data from four Phase III trials of Affymax/Takeda's Hematide (peginesatide), for the treatment of anaemia in chronic renal failure, show that the drug met all its primary endpoints, but ...
 
ThromboGenic's microplasmin met its primary endpoint – resolution of vitromacular adhesion (VMA) – in patients with the eye disease. The study results, presented at the American Society of Retina ...
Otonomy, a private US biopharmaceutical company focused on disorders of the inner and middle ear, has raised $38.5 million in a series B round. The company said the funds would be used to support its ...
Novartis has completed its acquisition of a 52% stake in the eyecare firm Alcon from Nestlé. The Swiss pharma giant paid $28.3 billion for the stake, taking its total share of Alcon up to 77%. It ...
 
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