Press Releases
- Wed, 04 Jan 2012 14:04:00 GMTAVI BioPharma Data Safety Monitoring Board Reports No Safety Concerns Identified in Phase IIb DMD Clinical Trial, Recommends Continuation of Trial
- Wed, 14 Dec 2011 22:12:00 GMTAVI BioPharma Receives NASDAQ Notice of Minimum Bid Price Non-Compliance
Lead Program: Duchenne Muscular Dystrophy
AVI’s exon skipping therapy exhibits first ever reported generation of dystrophin-positive muscle fibers of more than 50% of normal in a patient after systemic delivery. read more >
