Study to Determine if BHV-1300 is Effective and Safe in Adults With Graves' Disease

NCT07661056Phase 3Recruiting

Lead sponsor
Biohaven Therapeutics Ltd. (Industry)
Enrollment
300 (estimated)
Start date
26 Jun 2026
Primary completion
Jan 2028 (estimated)
Study completion
1 Feb 2028
Last update posted
19 Oct 2026

Design

Study type
Interventional
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel
Masking
Quadruple
Arms
2

Interventions

  • BHV-1300 Drug
  • Placebo Drug

Conditions and primary outcome

  • Graves Disease

Primary outcome

Number of participants on BHV-1300 vs placebo who are not on an antithyroid drug and with normal thyroid function (total T3, free T4 (FT4), & TSH within normal limits) at Week 26. (Week 26)

Posted results on ClinicalTrials.gov

Results posted on ClinicalTrials.gov: No

Results from company and journal sources

No editor-confirmed results are on record for this study.

Publications

No PubMed citation lists NCT07661056.

CT-VCA trial quality

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Data integrity

Compare what the registry, company releases, FDA documents and publications say about this study.

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Source

Source: ClinicalTrials.gov, U.S. National Library of Medicine. Listing a study does not mean NLM has evaluated it.

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