Biohaven
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Biohaven (BHVN) investor relations material

Biohaven Q2 2026 earnings summary

Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
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Q2 2026 earnings summary10 Aug, 2026

Executive summary

  • Achieved significant clinical milestones, including advancing BHV-1300 into Phase 3 for Graves' disease, presenting compelling data for Graves' disease and IgA nephropathy, and reporting durable seizure control for opakalim in epilepsy.

  • Completed enrollment in pivotal epilepsy and obesity trials, with topline results expected in H2 2026.

  • Expanded oncology pipeline with new data for BHV-1530 and advanced collaborations for ADC programs.

  • No revenue generated from product sales; operations funded by equity and debt financings.

  • Strategic reprioritization in Q4 2025 to optimize costs and value generation.

Financial highlights

  • Net loss for Q2 2026 was $137.3M ($0.91/share), improved from $198.1M ($1.94/share) in Q2 2025.

  • R&D expenses for Q2 2026 were $100.8M, down from $184.4M in Q2 2025, reflecting strategic reprioritization and lower milestone payments.

  • G&A expenses for Q2 2026 were $24.1M, down from $27.3M year-over-year.

  • Cash, cash equivalents, and marketable securities at June 30, 2026 totaled $270.5M.

  • Non-GAAP adjusted net loss for Q2 2026 was $118.1M ($0.78/share), compared to $166.4M ($1.63/share) in Q2 2025.

Outlook and guidance

  • Pivotal Phase 3 readouts for BHV-1300 in Graves' disease and opakalim in epilepsy expected in H2 2026.

  • Pivotal study for BHV-1400 in IgA nephropathy to initiate in H2 2026.

  • Cash, cash equivalents, and marketable securities expected to fund operations for at least one year from the report date.

  • Continued advancement of pipeline candidates in neurology, immunology, and oncology.

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Frequently asked questions

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.