RecruitingPhase 1NCT06980649

Study of BHV-1300 in Graves' Disease

An Open-Label Biomarker Study of BHV-1300 in Graves' Disease


Sponsor

Biohaven Therapeutics Ltd.

Enrollment

15 participants

Start Date

Aug 21, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to determine if BHV-1300 is a safe treatment in participants with Graves' Disease and to explore its effect on disease-specific biomarkers.


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Inclusion Criteria1

  • \. Participants must have serologically confirmed Graves' Disease.

Exclusion Criteria2

  • History of hyperthyroidism not caused by Graves' Disease (e.g., toxic adenoma or toxic multinodular goiter) and/or history of thyroid storm within six weeks of the Baseline visit.
  • History of treatment with radioactive iodine or thyroid surgery.

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Interventions

DRUGBHV-1300

BHV-1300 is delivered subcutaneously (SC)


Locations(13)

Site-103

South Gate, California, United States

Site-100

Miami, Florida, United States

Site-104

Columbus, Georgia, United States

Site-106

Houston, Texas, United States

Site-101

Houston, Texas, United States

Site-105

Shavano Park, Texas, United States

Site-004

Fitzroy, Australia

Site-001

Kotara, Australia

Site-003

Melbourne, Australia

Site-010

Oaklands Park, Australia

Site-008

Parkville, Australia

Site-006

St Leonards, Australia

Site-002

Torquay, Australia

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NCT06980649


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