Overview
US biotechnology firm's Q1 2026 saw no revenue and net loss widened year-over-year
Company's lead therapy Deramiocel under FDA review with PDUFA target date August 2026
Cash position expected to fund operations into Q4 2027, excluding potential product sales
Outlook
Company expects FDA decision on Deramiocel BLA by August 22, 2026
Capricor expects cash balance to support operations into Q4 2027
Company preparing for potential Deramiocel launch; manufacturing expansion and stockpiling underway
Result Drivers
OPERATING EXPENSES - Higher research and development and administrative costs contributed to increased net loss in Q1
COMMERCIAL PREPARATIONS - Company expanded manufacturing capacity and prepared for potential Deramiocel launch, including facility expansion and hiring a Chief Commercial Officer
REGULATORY AND LEGAL ACTIVITIES - Ongoing FDA review of Deramiocel and legal action to address distribution agreement impacted operational focus
Company press release: ID:nGNX83jx95
Key Details
Metric
Beat/Miss
Actual
Consensus Estimate
Q1 EPS
-$0.59
Analyst Coverage
The current average analyst rating on the shares is "buy" and the breakdown of recommendations is 9 "strong buy" or "buy", no "hold" and no "sell" or "strong sell"
The average consensus recommendation for the biotechnology & medical research peer group is "buy"
Wall Street's median 12-month price target for Capricor Therapeutics Inc is $54.00, about 69.3% above its May 11 closing price of $31.90
For questions concerning the data in this report, contact Estimates.Support@lseg.com. For any other questions or feedback, contact reuters.support@thomsonreuters.com.
(This story was created using Reuters automation and AI based on LSEG and company data. It was checked and edited by a Reuters journalist prior to publication.)