Rhythm Pharmaceuticals Announces FDA Acceptance For Priority Review Of Supplemental NDA For IMCIVREE In Patients As Young As 2 Years Old
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Rhythm Pharmaceuticals announced that the FDA has accepted its supplemental NDA for IMCIVREE, targeting obesity in young children with specific genetic conditions. The FDA has granted a Priority Review with a decision expected by December 26, 2024.
August 26, 2024 | 12:05 pm
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Rhythm Pharmaceuticals' sNDA for IMCIVREE has been accepted for FDA Priority Review, potentially expanding its use to younger children with specific genetic obesity conditions. A decision is expected by December 26, 2024.
The FDA's acceptance of the sNDA for Priority Review is a positive development for Rhythm Pharmaceuticals, as it indicates the potential for an expanded market for IMCIVREE. The decision date set for December 26, 2024, provides a timeline for investors to anticipate potential impacts on the company's market position and stock price.
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