Biohaven Reports Recent Business Developments and Fourth Quarter and Full Year 2024 Financial Results
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Biohaven announced the FDA's acceptance and Priority Review of its NDA for troriluzole in treating spinocerebellar ataxia, with a PDUFA date expected in Q3 2025. The company reported $489 million in cash and equivalents as of the end of 2024.
March 03, 2025 | 12:45 pm
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Biohaven's NDA for troriluzole has been accepted for Priority Review by the FDA, with a decision expected in Q3 2025. This regulatory milestone could significantly impact the company's future revenue streams. Biohaven's strong cash position of $489 million provides financial stability.
The FDA's acceptance and Priority Review of Biohaven's NDA for troriluzole is a significant regulatory milestone, indicating potential approval and market entry, which could boost future revenues. The company's strong cash position further supports its operational stability.
CONFIDENCE 90
IMPORTANCE 80
RELEVANCE 100