Capricor Therapeutics Inc (NASDAQ:CAPR – Get Free Report) has been given a consensus recommendation of “Buy” by the six analysts that are covering the stock, Marketbeat reports. Six equities research analysts have rated the stock with a buy rating. The average 1 year price target among analysts that have covered the stock in the last year is $34.50.
Several brokerages have recently weighed in on CAPR. Piper Sandler started coverage on shares of Capricor Therapeutics in a research note on Monday, October 21st. They set an “overweight” rating and a $35.00 price target on the stock. HC Wainwright reaffirmed a “buy” rating and set a $77.00 price objective on shares of Capricor Therapeutics in a research report on Thursday, November 14th. Maxim Group raised their target price 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. Oppenheimer reissued an “outperform” rating and issued a $15.00 price objective on shares of Capricor Therapeutics in a research note on Monday, September 23rd. Finally, Cantor Fitzgerald lifted 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.
Check Out Our Latest Stock Analysis on CAPR
Hedge Funds Weigh In On Capricor Therapeutics
Capricor Therapeutics Stock Performance
CAPR opened at $14.08 on Thursday. The company’s 50 day moving average is $17.36 and its 200 day moving average is $10.57. The company has a market cap of $640.22 million, a price-to-earnings ratio of -13.28 and a beta of 3.98. Capricor Therapeutics has a 12-month low of $3.52 and a 12-month high of $23.40.
Capricor Therapeutics Company Profile
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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