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Pfizer plans to Investment $350M in a New World-Class Global Biotechnology Center in China

Pfizer Inc announced that it will invest approximately USD$350 million in the development of a state-of-the-art Global Biotechnology Center at a ground-breaking ceremony in the Hangzhou Economic Development Area (HEDA) in China. This innovative facility will...

Takeda Initiates World’s First Norovirus Vaccine Field Trial

Takeda announced that it has dosed the first subject in a Phase 2b field efficacy trial of Takeda’s norovirus vaccine candidate (TAK-214), the only norovirus vaccine candidate in human clinical trials. The Phase 2b, double-blind, randomized,...

7 th Edition of the Innovation Days: The must Partnering event in the Life Sciences

The Innovation Days are a unique international event focused on promoting innovation in the field of Life Sciences . For its 7th edition , this event will bring to Paris 600 innovators and health : pharmaceutical companies, startups ,...

Shire Receives FDA Breakthrough Therapy Designation for SHP621 and SHP625

Shire plc announced that the U.S. FDA has granted Breakthrough Therapy Designation for two investigational products for rare diseases: SHP621 (budesonide oral suspension, or BOS) for eosinophilic esophagitis (EoE), and SHP625 (maralixibat) for progressive familial intrahepatic cholestasis type 2...

Mallinckrodt Submits INDA For Synacthen Depot

Company will pursue an indication for the drug in treatment of Duchenne Muscular Dystrophy.Mallinckrodt plc a leading global specialty biopharmaceutical company, announced it has submitted an Investigational New Drug (IND) application for Synacthen® Depot to the U.S. Food and...

Pfizer Announces Final Results From Inotuzumab Ozogamicin Pivotal Phase 3 Study With Refractory Acute Lymphoblastic Leukemia

Pfizer Inc announced the publication of findings from the Phase 3 INO-VATE ALL study in the online issue of The New England Journal of Medicine. The study, also known as Study 1022, is an open-label, randomized,...

Ironwood and Allergan Announce New Drug Application for 72 mcg Linaclotide Has Been Accepted for FDA Review

Ironwood Pharmaceuticals, Inc.and Allergan plc announced that the U.S. FDA has accepted for review the supplemental New Drug Application (sNDA) for the 72 mcg dose of linaclotide for use in the treatment of adults with chronic idiopathic constipation (CIC)....

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