FDA's new accelerated approval guidance to benefit rare disease drug development, analysts believe
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The FDA's new guidance on accelerated approval for drugs targeting serious conditions is seen as a positive development for rare disease drug development, according to Jefferies analysts.
December 13, 2024 | 4:30 pm
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Sarepta Therapeutics (SRPT) could benefit from the FDA's new guidance on accelerated approval for drugs targeting serious conditions, as it focuses on rare diseases.
Sarepta Therapeutics is involved in developing treatments for rare diseases. The FDA's new guidance on accelerated approval for drugs targeting serious conditions could expedite the approval process for Sarepta's pipeline, potentially leading to faster market entry and revenue generation.
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IMPORTANCE 70
RELEVANCE 80