Biohaven
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Biohaven (BHVN) investor relations material

Biohaven Q4 2025 earnings summary

Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
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Q4 2025 earnings summary2 Mar, 2026

Executive summary

  • Prioritized three late-stage clinical programs: MODE/TRAP degraders for immunological diseases, Kv7 ion channel modulation for epilepsy, and myostatin-activin pathway targeting obesity.

  • Achieved clinical proof-of-concept for MODE/TRAP degraders, with strong efficacy signals in Graves' disease and IgA nephropathy.

  • Restructured business priorities in Q4 2025, focusing resources on key programs and reducing annual direct R&D spend by approximately 60%.

  • Advanced pipeline with positive early clinical data and initiated strategic partnerships and capital raising initiatives.

Financial highlights

  • Cash, cash equivalents, marketable securities, and restricted cash totaled $322.0 million as of December 31, 2025.

  • Net loss for Q4 2025 was $145.6 million ($1.21 per share), improved from $186.8 million ($1.85 per share) in Q4 2024.

  • Non-GAAP adjusted net loss for Q4 2025 was $107.9 million ($0.90 per share), compared to $173.3 million ($1.71 per share) in Q4 2024.

  • Full year 2025 net loss was $738.8 million ($6.86 per share), compared to $846.4 million ($9.28 per share) in 2024.

  • R&D expenses for 2025 were $635.1 million, down from $795.9 million in 2024, reflecting cost optimization and one-time 2024 expenses.

Outlook and guidance

  • Pivotal studies for BHV-1400 in IgA nephropathy and BHV-1300 in Graves' disease to initiate in 2026.

  • Topline results for opakalim in focal epilepsy and taldefgrobep in obesity expected in the second half of 2026.

  • Continued focus on financial discipline and capital preservation to support prioritized programs.

Degrader platform partnership strategy
Impact of trial acceleration on R&D savings?
Opakalim/Taldefgrobep competitive differentiation
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Biohaven Pharmaceutical Holding Company Ltd., a biopharmaceutical company, develops products candidates targeting neurological and neuropsychiatric diseases, and rare disorders in the United States. The company's product candidates are either in various stages of clinical trials or pre-clinical trials.

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