Bengaluru: The U.S. Food and Drug Administration approved Scholar Rock's therapy on Friday to treat a rare genetic condition that causes muscle weakness, marking the first regulatory approval for the company.

The injectable treatment, sold as Isembyld, is the first muscle-targeted ‌therapy designed ⁠to ⁠improve motor function for adults and children with spinal muscular atrophy who have been treated with existing therapies for the condition.

Scholar Rock shares rose over 23% in after-market ​trading. The company said Isembyld will be available in the coming days but did not immediately respond to a Reuters request for comment on ​pricing details.

Spinal muscular atrophy is a genetic ⁠disorder that ‌damages motor neurons, causing progressive muscle weakness and problems with ​movement, breathing ​and swallowing.

The condition is estimated to affect roughly 10,000 ⁠children and adults in the United States, according to ​the Muscular Dystrophy Association.

Cantor analysts said Isembyld's approval sets ​up Scholar Rock to be one of the best long-term growth stories in biotech based on geographic, indication and product line expansions.

Chemically known as apitegromab, Isembyld selectively blocks activation of myostatin, a protein that limits muscle growth, with the aim of increasing muscle mass and strength.

The ‌approval was based on late-stage data that showed the therapy significantly improved motor function for patients with the condition compared ​with placebo. It ​will compete with ⁠Biogen's Spinraza, Novartis' gene therapy Zolgensma and Roche's oral Evrysdi.

The company has previously said it would use a U.S.-based manufacturing facility for Isembyld. BMO Capital Markets analyst ​Evan Seigerman forecasts 2035 adjusted worldwide peak sales of $2.1 billion for the drug.

Scholar Rock is also testing the drug to preserve muscle in obesity, competing with more than a dozen companies developing treatments aimed at minimizing muscle loss during weight loss.

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Article Source : Reuters

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