Genzyme Strengthens Endocrinology Portfolio with Acquisition of Rare Disease Therapy Caprelsa®(vandetanib) from AstraZeneca Paris, France, 30-7-2015 — /EuropaWire/ — Sanofi and its subsidiary Genzyme announced today that it has entered into a definitive agreement with AstraZeneca to acquire Caprelsa® (vandetanib), a … Read the full press release
Posted in Business, France, Healthcare, Management, Pharma & Biotech
Tagged AstraZeneca, Caprelsa® (vandetanib), Genzyme, Luke Miels, Sanofi
Investigational Enzyme Replacement Therapy to Treat Non-Neurological Manifestations which characterize Niemann-Pick Type B PARIS, 5-6-2015 — /EuropaWire/ — Sanofi and its subsidiary Genzyme announced today that the U.S. Food and Drug Administration (FDA) has granted Breakthrough Therapy designation to olipudase alfa. … Read the full press release
Posted in France, Pharma & Biotech, Science
Tagged Breakthrough Therapy, Genzyme, Niemann-Pick Type B, olipudase alfa, Richard Peters, Sanofi, sphingomyelin, US FDA
Approval Establishes Genzyme’s MS Franchise in the U.S. with Two Approved Products; Follows Global Approvals PARIS, 17-11-2014 — /EuropaWire/ — Sanofi and its subsidiary Genzyme announced today that the U.S. Food and Drug Administration (FDA) has approved LemtradaTM (alemtuzumab) for … Read the full press release
Posted in France, Healthcare, Pharma & Biotech
Tagged David Meeker, Dr. Timothy Coetzee, Edward Fox, FDA, Genzyme, LemtradaTM (alemtuzumab), M.D., multiple sclerosis (MS), Ph.D., Sanofi
In approximately 70 percent of patients, disability scores improved or remained stable for an additional two years beyond the two-year pivotal multiple sclerosis studies Approximately 70 percent of patients treated with Lemtrada did not receive a third course of treatment … Read the full press release
Posted in France, Healthcare, Pharma & Biotech
Tagged Genzyme, Lemtrada™ (alemtuzumab) for multiple sclerosis, Sanofi
Only First-Line Oral Treatment for Adult Gaucher Disease Type 1 Paris, 22-8-2014 — /EuropaWire/ — Genzyme, a Sanofi company (EURONEXT: SAN and NYSE: SNY), announced today that the U.S. Food and Drug Administration (FDA) has approved Cerdelga™ (eliglustat) capsules, the only … Read the full press release
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