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Dec 31, 2022

Biohaven Q4 2022 Earnings Report

Reported financial results for Q4 2022 and provided a review of recent accomplishments and anticipated upcoming milestones.

Key Takeaways

Biohaven Ltd. reported a net loss of $201.1 million for the three months ended December 31, 2022. As of December 31, 2022, the company had cash and equivalents of $465.3 million and no debt. The company is focused on advancing its pipeline of therapies for neurological and neuropsychiatric diseases.

Acquired exclusive license for oral, brain-penetrant, dual TYK2/JAK1 inhibitor for immune-mediated brain disorders in March 2023 covering global (ex-China) rights.

Completed Phase 1 SAD/MAD study with BHV-7000 from Kv7 ion channel activator platform and reported preliminary safety and tolerability data.

Commenced enrollment in pivotal Phase 3 study with myostatin targeting agent, adnectin taldefgrobep alfa, for spinal muscular atrophy.

Presented preclinical data from IgG degrader, BHV-1300, showing robust reduction of IgG levels.

Total Revenue
-$215M
Previous year: $190M
-213.2%
EPS
-$1.27
Previous year: -$2.32
-45.3%
Cash and Equivalents
$465M
Previous year: $76.1M
+511.8%
Free Cash Flow
-$75.7M
Previous year: -$33.3M
+127.6%
Total Assets
$662M
Previous year: $142M
+365.8%

Biohaven

Biohaven

Forward Guidance

Biohaven is progressing its product candidates through clinical programs in a number of common and rare disorders and expects to reach significant pipeline milestones in the coming periods.

Positive Outlook

  • Initiate EEG study with BHV-7000 in the first half of 2023
  • Submit IND with BHV-7010 in epilepsy and mood disorders in the second half of 2023
  • Submit IND with BHV-2100 in chronic pain in 2023
  • Commence Phase 1 studies with BHV-8000 in 2023
  • Complete enrollment in Phase 3 study of troriluzole in OCD in 2023