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Biohaven ($BHVN) is on the verge of a historic FDA decision for Troriluzole, a potential first-ever treatment for the devastating rare disease, Spinocerebellar Ataxia (SCA). The leadership team at Biohaven is the same one that developed a blockbuster migraine drug and sold it to Pfizer for a massive $11.6 billion. With a PDUFA date set for Q4 2025, this is a make-or-break moment for the company. Will this proven team deliver another grand slam for patients and investors? In this deep dive, we break down everything you need to know about this high-stakes biotech play. We'll explore: The Disease: An overview of Spinocerebellar Ataxia (SCA), a cruel, inherited condition with zero FDA-approved treatments. The Drug: How Biohaven's once-daily pill, Troriluzole, works to protect the brain by modulating glutamate. The Data: A look at the innovative real-world evidence study that showed Troriluzole slowed disease progression by 50% to 70% over three years. The Financials: An analysis of Biohaven's balance sheet, their high cash burn rate, and what a potential approval or rejection could mean for the stock price. Valuation Scenarios: We break down the Bull Case ($59/share) , Base Case ($29/share) , and Bear Case ($7/share) for BHVN stock. This is a classic, binary biotech investment where a single FDA decision could change everything. Disclaimer: This video is for informational purposes only and is not financial advice. I am not a financial advisor. All investment decisions should be made based on your own due diligence and consultation with a professional. What are your thoughts on Biohaven and its chances for FDA approval? Let me know in the comments below! #Biohaven #BHVN #Biotech #Investing #Stocks #FDA #SpinocerebellarAtaxia #SCA #StockMarket #Neuroscience