Shares of Capricor Therapeutics Inc (NASDAQ:CAPR – Get Free Report) have been given an average rating of “Buy” by the six brokerages that are presently covering the firm, Marketbeat Ratings reports. Six equities research analysts have rated the stock with a buy rating. The average twelve-month target price among analysts that have issued ratings on the stock in the last year is $34.50.
Several research analysts have recently weighed in on CAPR shares. Oppenheimer reaffirmed an “outperform” rating and issued a $15.00 price target on shares of Capricor Therapeutics in a report on Monday, September 23rd. Piper Sandler initiated coverage on Capricor Therapeutics in a report on Monday, October 21st. They issued an “overweight” rating and a $35.00 price target on the stock. HC Wainwright reissued a “buy” rating and set a $77.00 price objective on shares of Capricor Therapeutics in a report on Thursday, November 14th. Cantor Fitzgerald raised their target price on shares of Capricor Therapeutics from $25.00 to $30.00 and gave the company an “overweight” rating in a research note on Thursday, November 14th. Finally, Maxim Group boosted their price target on shares of Capricor Therapeutics from $12.00 to $25.00 and gave the stock a “buy” rating in a research note on Wednesday, September 25th.
Check Out Our Latest Stock Report on CAPR
Institutional Trading of Capricor Therapeutics
Capricor Therapeutics Trading Down 0.8 %
Capricor Therapeutics stock opened at $14.01 on Thursday. Capricor Therapeutics has a 1-year low of $3.52 and a 1-year high of $23.40. The firm has a market capitalization of $637.03 million, a PE ratio of -13.22 and a beta of 3.98. The firm’s 50 day simple moving average is $17.68 and its 200 day simple moving average is $10.46.
About Capricor Therapeutics
Capricor Therapeutics, Inc (NASDAQ:CAPR) is a clinical-stage biotechnology company focused on the discovery, development and commercialization of first-in-class biological therapeutics for the treatment of rare disorders. Capricor’s lead candidate, CAP-1002, is an allogeneic cell therapy that is currently in clinical development for the treatment of Duchenne muscular dystrophy.
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