
Shares of therapy developer Capricor Therapeutics CAPR.O rise 16.8% to $8.97
Co says the U.S. FDA has indicated that an advisory panel review is not required for its cell therapy deramiocel
The company is seeking approval for the therapy as a potential treatment for patients with a heart disease commonly associated with the muscle weakness condition called Duchenne muscular dystrophy
Last month, the company said the health regulator will hold a panel meeting for deramiocel, causing shares to drop about 13%
The FDA is set to make its decision on August 31
Including session's move, stock down 40.5% YTD