Larimar Therapeutics IncFDA confirms existing data sufficient for BLA submission, supporting accelerated approval path.

Larimar Therapeutics has submitted the initial module of its Biologics License Application to the U.S. FDA seeking accelerated approval for its Nomlabofusp therapy. The company plans to submit the remaining modules during the second half of 2026. The therapy showed positive outcomes in an open-label study of adult patients receiving daily injections for Friedreich's ataxia, and the FDA confirmed that existing data based on the surrogate endpoint of skin frataxin is sufficient to support the application. Separately, Baird analyst Christopher Chen lowered his price target on the stock from $7 to $5 while maintaining an Outperform rating, citing therapy updates that indicate clinical benefits but also carry safety concerns.
Larimar Therapeutics IncFDA confirms existing data sufficient for BLA submission, supporting accelerated approval path.