Top Regulatory News Stories – Week Ending May 3, 2019
The U.S. FDA gave Sanofi’s dengue vaccine Dengvaxia a very narrow approval on Wedneday. The company continues to suffer from evidence that its vaccine, which took 20 years to develop, can cause severe infections in some people. https://www.reuters.com/article/us-usa-fda-sanofi-fr/sanofi-wins-fda-approval-to-sell-dengue-shot-in-parts-of-u-s-idUSKCN1S74TI?feedType=RSS&feedName=healthNews Finch Therapeutics Group announced that the FDA has granted Fast Track designation to its Full-Spectrum Microbiota® (FSM®)[…]