RecruitingPhase 3NCT07661056

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

A Phase 3, Double-blind, Multicenter, Randomized, Placebo-Controlled Study to Evaluate the Efficacy, Safety and Tolerability of BHV-1300 in the Treatment of Adults With Graves' Disease


Sponsor

Biohaven Therapeutics Ltd.

Enrollment

300 participants

Start Date

Jun 26, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to evaluate the efficacy and safety of BHV-1300 in adult participants with Graves' disease who are actively hyperthyroid


Eligibility

Min Age: 18 YearsMax Age: 70 Years

Inclusion Criteria2

  • Participants must have serologically confirmed Graves' disease as documented by presence of elevated autoantibodies
  • Participants must have active hyperthyroidism due to Graves' disease

Exclusion Criteria7

  • History of hyperthyroidism not caused by Graves' Disease (e.g., toxic adenoma or toxic multinodular goiter)
  • History of treatment with radioactive iodine or thyroid surgery.
  • Have received levothyroxine, desiccated thyroid extract, or T3 at any dose within six weeks of the Baseline/Day 1 Visit.
  • Thyroid storm, i.e. severe thyrotoxicosis with evidence of systemic decompensation (e.g., Burch-Wartkofsky Point Scale of ≥ 45 or Japanese Thyroid Association category 1 or 2, with accompanying manifestations including hyperpyrexia, tachycardia, arrhythmias, congestive heart failure, agitation, delirium, psychosis, stupor, and coma, as well as nausea, vomiting, diarrhea, or hepatic failure) within 6 weeks of Screening.
  • Have autoimmune disease other than Graves' disease requiring treatment
  • Have moderate to severe thyroid eye disease (TED) and are expected to require immediate surgical intervention and/or are planning corrective surgery/irradiation or medical therapy for TED during study participation.
  • Are expected to require urgent or emergent thyroid surgery or ablation within six weeks of Baseline/Day 1 or throughout the study.

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Interventions

DRUGBHV-1300

delivered subcutaneously via autoinjector

DRUGPlacebo

delivered subcutaneously via autoinjector


Locations(15)

Site-032

Burbank, California, United States

Site-006

San Diego, California, United States

Site-067

Walnut Creek, California, United States

Site-052

Doral, Florida, United States

Site-019

Hialeah, Florida, United States

Site-025

Lenexa, Kansas, United States

Site-064

Morehead City, North Carolina, United States

Site-008

Canton, Ohio, United States

Site-055

Dallas, Texas, United States

Site-043

Denton, Texas, United States

Site-042

El Paso, Texas, United States

Site-071

Houston, Texas, United States

Site-054

McKinney, Texas, United States

Site-013

Layton, Utah, United States

Site-073

Midlothian, Virginia, United States

View Full Details on ClinicalTrials.gov

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NCT07661056


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