Shots:
- The P-II REACH-CDM evaluate the efficacy and safety of AMO-02 (tideglusib) in 56 patients to treat congenital Myotonic Dystrophy in the U.S and Canada with additional sites in Australia, New Zealand, and other countries to be added seeking local approvals
- The REACH-CDM study was designed on the basis of positive P-II data results which were recently published in the peer-reviewed journal Pediatric Neurology.
- AMO-02 is a clinical-stage investigation medicine & in development for the treatment of congenital myotonic dystrophy and has potential use in CNS, neuromuscular and other orphan indications
Click here to read full press release/ article | Ref: PRNewswire | Image: The Pharma Letter
The post AMO Pharma Initiates P-II REACH-CDM study of AMO-02 (tideglusib) to treat Congenital Myotonic Dystrophy first appeared on PharmaShots.
