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Capricor’s Duchenne drug gets three-month FDA extension after new data submission

By Thomson Reuters Aug 24, 2026 | 8:39 AM

By Kamal Choudhury

Aug 24 (Reuters) – Capricor Therapeutics said on Monday the U.S. Food and Drug Administration had extended the review period for its experimental cell therapy for Duchenne ​muscular dystrophy by three months.

The delay follows Capricor’s submission ‌of new 24-month data from its late-stage study, along with extra analyses, to support a refined proposed indication focused on upper limb function, the trial’s main goal.

The therapy, deramiocel, last year failed to get FDA’s approval to ‌treat ​cardiomyopathy, or a heart muscle disease, ⁠in patients with Duchenne muscular ⁠dystrophy. The regulator said the treatment did not meet efficacy requirements and asked for more data.

Earlier this year, Capricor resubmitted its application with new data, and was expecting a decision ​by August 22.

But last month, an FDA advisory panel voted against the therapy’s effectiveness data, while the agency staff flagged ⁠concerns about changes to how the ⁠company measured trial results.

Following this, Capricor Chief Executive ​Linda Marban said the company will submit an amendment with new ​data focused on improving upper limb muscle function.

The health ‌regulator has accepted the amendment, citing the high unmet medical need for Duchenne patients, and classified the submission as a “major amendment” and set the new deadline to November 22, Capricor said.

Shares of ⁠the company rose 15% to $7.25.

Marbán said the additional follow-up data gives the company “one of the most extensive clinical datasets evaluating upper limb function ⁠in Duchenne,” and that ‌the trial had met its main goal ⁠with a statistically significant benefit.

Deramiocel is being developed ​to ‌treat Duchenne, a rare genetic disease that affects ​about 15,000 ⁠people in the United States, primarily boys.

The key question remains whether the new data and analyses are sufficient to “address the FDA’s concerns and support approval for the refined indication focused on upper limb function,” said H.C. Wainwright analysts.

(Reporting by Kamal Choudhury in Bengaluru; Editing ​by Shinjini Ganguli)