Genzyme Receives Positive Opinion for European Approval of Mozobil
Genzyme Corp. (Nasdaq: GENZ) announced that the European Medicines Agency's Committee for Human Medicinal Products (CHMP) has adopted a positive opinion on the marketing authorization application for Mozobil ® (plerixafor injection). The committee's opinion will be forwarded to the European Commission, which will make a final decision on the authorization. The Commission has 66 calendar days to act on the CHMP's opinion.
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Nycomed Reports a Solid Start to 2009
Nycomed reports a solid start to 2009, with total net turnover increasing by 1.2% to €839.9 million, despite adverse impact from currency movements. Excluding the effects of currency, the increase was 3.8%, underlining the solid performance of the main product Pantoprazole and other key products. On a regional basis, most Nycomed markets performed in line with or above expectations.
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Roche announces new two-year data from the LITHE study
Roche has announced that new two-year data from the LITHE study(1) demonstrate that ACTEMRA (tocilizumab, known as RoACTEMRA within the EU) continues to be highly effective at inhibiting joint structural damage and maintaining consistently high remission rates. Reducing the structural damage to joints in patients with rheumatoid arthritis (RA) is a critical measure of effectiveness of an RA treatment.
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Sandoz to acquire EBEWE Pharma specialty generics business
Novartis has signed a definitive agreement to acquire the specialty generic injectables business of EBEWE Pharma, providing Sandoz - the Group's generic pharmaceuticals division - an opportunity to create a strong global platform for future growth while improving access for patients worldwide to many generic oncology medicines.
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Abbott's XIENCE V(R) Demonstrates Impressive Results in SPIRIT V Study
New data presented at EuroPCR from an international, post-approval, single-arm study show that Abbott's market-leading XIENCE V(R) Everolimus Eluting Coronary Stent System demonstrated low rates of repeat procedure (target lesion revascularization), stent thrombosis and major adverse cardiac events (MACE) in a complex patient population.
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Sanofi-aventis introduces sanofi-aventis TV "A window on our company"
Sanofi-aventis (EURONEXT: SAN and NYSE: SNY) has announced the launch of sanofi-aventis TV, a new webTV aimed at providing information about the company's wide range of patient-focused businesses, social responsibilities, and employee activities. The site will also provide perspectives on the company's mission and strategic directions.
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New data to be presented on Abbott's market-leading XIENCE V(R) stent
Abbott (NYSE: ABT) has announced the company's schedule of major events and news announcements during EuroPCR 2009 in Barcelona, May 19 - 22. These include the presentation of new data from the SPIRIT V post-approval, single-arm study of the company's market-leading XIENCE V(R) Everolimus Eluting Coronary Stent System, as well as new details of Abbott's next-generation drug eluting stent in development,
the XIENCE PRIME(TM) Everolimus Eluting Coronary Stent System.
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