ALS Biopharma Press Release


Doylestown, PA. July 5, 2016:

ALS Biopharma, LLC is pleased to announce that the U.S. Food and Drug Administration (FDA) has completed its review of the FC-4157 (also known as BHV-4157) investigational new drug application (IND) filed on May 31, 2016 by Biohaven Pharmaceutical Holding Company Ltd. (“Biohaven”), and informed Biohaven that clinical trials in humans may proceed, as noted on Yahoo Finance (see here). FC-4157 was first prepared at Fox Chase Chemical Diversity Center, Inc. by work funded by SBIR grants from the National Institutes of Health (R44CA156781), in collaboration with ALS Biopharma, and is currently being developed by Biohaven for multiple indications.




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