(Reuters) -The U.S. health regulator has declined to approve Scholar Rock's drug for a rare neuromuscular disease citing issues at a third-party manufacturing facility, the company said on Tuesday.
Shares of the drug developer were down 14% in premarket trading.
Scholar Rock is banking on apitegromab to drive its growth and profitability. The drug is being tested as a treatment for spinal muscular atrophy and muscle preservation in obesity.
Analysts estimate that apitegromab, once approved, could bring in nearly $2 billion in revenues by early 2030s.
The U.S. Food and Drug Administration's so-called complete response letter is related to issues identified during a routine inspection of Catalent's Indiana fill-finish facility, which was acquired by Novo Nordisk, the company said. The agency's observations were not specific to the drug, it added.
Regeneron's drugs have lately been impacted by delays and rejections, following the agency's site inspections at Catalent's Indiana facility.
Scholar Rock said it will resubmit its application seeking marketing approval for apitegromab, after Catalent fixes the issues raised by the FDA.
There were no other approvability issues cited by in the regulator's letter, it added.
Spinal muscular atrophy is the leading genetic cause of infant deaths and affects about 1 in 10,000 people, according to U.S. government data. It prevents the body from producing a protein necessary for neuromuscular development and leaves children too weak to walk, talk and swallow.
Scholar Rock is competing with at least a dozen other companies in the race to develop treatments that can help people shed weight without losing muscle.
The use of these muscle-preserving treatments is expected to grow with the use of GLP-1 drugs for obesity, such as the wildly popular Zepbound and Wegovy injections from Eli Lilly and Novo Nordisk, respectively.
(Reporting by Sriparna Roy, Christy Santhosh, Bhanvi Satija and Puyaan Singh in Bengaluru; Editing by Shailesh Kuber)
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