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The approval, including in the UK, Germany and Spain, is for the biosimilarity study part of the phase 3 program, which is designed to allow interchangeability with Humira

The study demonstrated that Keytruda was superior to chemotherapy as measured by progression-free survival (PFS) and overall survival (OS). Based on the positive results, the independent data monitoring

The five-story, 175,000-square-foot addition to Pfizer’s Andover campus is expected to be completed in January 2019. The facility will house about 75 employees who will produce vaccines and

The randomized, controlled, blinded, cross-over study is designed to evaluate the safety and efficacy of FLX-787, the Company’s single molecule, chemically synthesized, transient receptor potential (TRP) ion channel

If approved, Carbylan will be renamed KalVista Pharmaceuticals, Inc. The transaction has been unanimously approved by the boards of directors of both companies. Carbylan’s three largest shareholders, InterWest

The financing will support clinical development of Rgenix’s lead drug candidates, RGX-104 and RGX-202, as well as further development of its therapeutics pipeline. "We are thrilled to have

This is the first program to enter clinical testing out of the discovery collaboration between the two companies. The molecule being advanced in clinical testing was discovered by

Existing investors Forbion Capital Partners, Edmond de Rothschild Investment Partners, EMBL Ventures and Allecra’s co-Founder Nicholas Benedict also participated in the round. Allecra will use the proceeds for

Kamada and Baxalta (formerly Baxter International’s BioScience business and now part of Shire) entered into a cooperation agreement in 2010 for the distribution and license of Glassia, which