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flag FDA approves Forzinity for Barth syndrome, the first treatment for the rare genetic disorder, based on improved muscle function in trials.

flag The FDA has granted accelerated approval to Forzinity (elamipretide) for Barth syndrome, a rare genetic disorder affecting primarily males, marking the first treatment for the condition. flag Approved on September 19, 2025, the drug improves mitochondrial function and is based on clinical trial results showing enhanced muscle strength and physical performance. flag It is currently approved for patients aged 12 and older weighing at least 66 pounds, with ongoing efforts to expand access to younger individuals. flag The approval follows years of delays and advocacy from families, and requires a post-approval trial to confirm long-term benefits. flag Common side effects are mild injection-site reactions.

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