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Biohaven (BHVN) investor relations material
Biohaven Q3 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Focused on immunology, neuroscience, and oncology, with reprioritization to three key clinical programs: Kv7 ion channel modulation, MODE/TRAP protein degraders, and myostatin-activin pathway agents, including opakalim, BHV-1300, and BHV-1400.
Advanced late-stage clinical programs in epilepsy, depression, autoimmune disease, obesity, and cancer, with several Phase 1–3 trials ongoing or planned.
Initiated strategic cost optimization, prioritizing high-value programs and reducing annual direct R&D spend by approximately 60%.
Restructured business priorities, pausing or halting non-priority programs to optimize resource allocation.
No product revenue to date; operations funded by equity and debt, including a $250M note issuance in April 2025.
Financial highlights
Net loss of $173.4M for Q3 2025 ($1.64 per share), compared to $160.3M in Q3 2024; net loss of $593.3M for the nine months ended September 30, 2025.
R&D expenses were $141.2M in Q3 2025 (down $16.4M YoY), and $513.1M for the nine months (down $115.3M YoY, mainly due to a one-time $171.9M expense in 2024 for a milestone/royalty buyback).
G&A expenses increased to $28.2M in Q3 2025 (up $7.7M YoY), and $89.5M for the nine months (up $22.7M YoY), driven by higher share-based compensation and legal costs.
Cash, cash equivalents, marketable securities, and restricted cash totaled $263.8M as of September 30, 2025.
Non-GAAP adjusted net loss for Q3 2025 was $155.9M ($1.47 per share), compared to $164.1M ($1.74 per share) in Q3 2024.
Outlook and guidance
Cash, equivalents, marketable securities, and equity commitments expected to fund operations for at least one year from issuance.
Additional capital will be required to execute business plans and pursue growth; future funding may come from equity, debt, or strategic transactions.
Top-line results from Phase 2 study of opakalim in major depressive disorder expected in Q4 2025.
Initial top-line results from two Phase 2/3 studies in focal epilepsy anticipated in 1H 2026.
Phase 2 clinical trial for taldefgrobep alfa in obesity to begin in Q4 2025.
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Record HST orders and margin gains support 2026 growth outlook amid macro uncertainties. - PFGC
Q2 and first-half 2026 saw 5.2% sales growth and 45.5% higher net income, with updated guidance. - CB
Record earnings, premium growth, and strong outlook driven by digital and global expansion. - COR
Q1 FY2026 revenue up 5.5% to $85.9B; adjusted EPS rose 9.4% to $4.08. - MATW
Leverage below 3x, Q1 net income $43.6M, FY2026 EBITDA guidance at $180M. - SU
Record production, strong cash returns, and robust 2026 guidance highlight performance. - GARAN
Net income up 21% to TL 111.3bn, with strong capital, liquidity, and asset growth. - ABBV
Record $61.2B sales, $10.00 EPS, and 2026 EPS guidance of $14.37–$14.57. - IAC
Q4 2025 digital revenue up 14%, Adjusted EBITDA up 29%, and $337M in share buybacks. - VLTO
Record 2025 growth and cash flow, with 2026 set for further gains and margin expansion.
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