Actively Recruiting
Open-Label Phase 1 Study of BHV-1300 Injection for Treating Graves Disease in Adults
Led by Biohaven Therapeutics Ltd. · Updated on 2026-07-31
15
Participants Needed
18
Research Sites
N/A
Total Duration
AI-Summary
What this Trial Is About
Researchers are studying the safety of BHV-1300 as a treatment for adults with Graves Disease. This Phase 1 trial aims to explore how BHV-1300 affects biomarkers related to this condition to better understand its impact. The study is led by Biohaven Therapeutics Ltd. and focuses on monitoring the treatments safety profile over time. Participants will receive BHV-1300, which is given as a subcutaneous injection. This open-label study does not include placebo control or blinding, and all participants receive the same treatment. The treatment period and follow-up extend up to 52 weeks to observe effects and any adverse events. During the study, participants will be closely monitored for serious adverse events, side effects that may lead to stopping treatment, and laboratory abnormalities. Researchers will regularly assess health status and collect data on disease-specific biomarkers. The total duration of participation is approximately one year, ensuring comprehensive safety and effect evaluations.
CONDITIONS
Brief Title
Study of BHV-1300 in Graves' Disease
Research Team
C
Chief Medical Officer
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