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FDA rejects apitegromab for SMA due to manufacturing issues, not safety or efficacy.
The FDA issued a Complete Response Letter rejecting Scholar Rock’s application for apitegromab, a treatment for spinal muscular atrophy, citing manufacturing issues at Catalent Indiana, a third-party facility.
The decision, based on inspection findings, does not question the drug’s safety or efficacy.
Scholar Rock plans to resubmit its application after the facility addresses the concerns.
The company remains committed to bringing the treatment to patients, and its shares dropped over 12% in pre-market trading.
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La FDA rechaza el apitegromab para la AME debido a cuestiones de fabricación, no de seguridad o eficacia.