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According to FDA, the submitted data and protocol amendments support the fact that there are no subject protection concerns that preclude continuation of the trials. So far, the

The NDA is based on data from eight clinical trials, including a Phase III program that was conducted under a Special Protocol Assessment as well as a Phase

The positive ACD is based on a thorough review of the clinical effectiveness of 2.5mg rivaroxaban twice daily in the randomized controlled landmark ATLAS ACS 2 TIMI 51

As previously announced, Islet Sciences and BHV have entered into a merger agreement that will combine the operations and development pipelines of the two companies. Upon closing of

Following a recent meeting with the U.S. Food and Drug Administration (FDA), Vaxart anticipates commencing human clinical trials in the first quarter of 2015. Start of Clinical Trials

The allowed claims cover inhibitors of PRMT5 and methods of cancer treatment with PRMT5 inhibitors. PRMT5 is implicated in several cancers, including blood cancers. Epizyme also announced the

Under the license agreement, Medivation will be responsible for all development, regulatory and commercialization activities for pidilizumab for all indications, including oncology. "Immuno-oncology is a significant area of

The new research centre, which will include four integrated office/laboratory buildings of different heights, will house around 1900 workplaces and is scheduled to be completed between 2021 and

Under the deal, Zymeworks would receive the majority of $375m in potential rewards related to development and commercial milestones. The initial up-front payment, which Zymeworks will receive in