A Study of IMVT-1402 for Graves' Disease

This study is testing a new drug called IMVT-1402 for adults with Graves' disease (an autoimmune disorder that causes an overactive thyroid) who are still experiencing symptoms despite taking their current antithyroid medication. Researchers want to see if IMVT-1402 is effective, safe, and well-tolerated. You might be able to join if you are between 18 and 75 years old and have Graves' disease that isn't fully controlled by your current medication. The study will compare two different doses of IMVT-1402 to a placebo (an inactive substance) over 26 weeks. Success in this study means participants become euthyroid (have normal thyroid hormone levels) and can stop their antithyroid medication by Week 26. The current recruitment status is unclear.

Study design
This is a Phase 2b, multi-center, global study that will randomly assign about 210 participants to receive either IMVT-1402 or a placebo. It is a double-blind study, meaning neither you nor your doctor will know which treatment you are receiving.
What's involved
You would receive either IMVT-1402 or a placebo for 26 weeks. Other specific procedures are not detailed here.
Compensation
Not stated in the trial record.
Follow-up
The primary outcome is measured at Week 26, which suggests follow-up for at least that duration.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07018323

A Study to Assess the Efficacy, Safety, and Tolerability of IMVT-1402 as Treatment for Adult Participants With Graves' Disease

Recruiting
PHASE2Ages 18–75InterventionalTreatment
Immunovant Sciences GmbH
~210 participants
Updated 2026-08-25 on ClinicalTrials.gov
What's tested:IMVT-1402Placebo

At a glance

Recruiting sites
163 of 163 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Percentage of participants who are euthyroid and off ATD at Week 26 (Dose 1)
Measured over Week 26
Graves' Disease

NCT07018323

Where you'd take part

This study runs at 163 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Site Nnumber - 3003

    Wroclaw, Polandno site contact published

    Recruiting

  • Site Number - 1000

    Miami, Floridano site contact published

    Recruiting

  • Site Number - 1001

    Morehead City, North Carolinano site contact published

    Recruiting

  • Site Number - 1002

    El Paso, Texasno site contact published

    Recruiting

  • Site Number - 1003

    Fort Worth, Texasno site contact published

    Recruiting

  • Site Number - 1004

    Kansas City, Missourino site contact published

    Recruiting

  • Site Number - 1007

    Oklahoma City, Oklahomano site contact published

    Recruiting

  • Site Number - 1008

    Hialeah, Floridano site contact published

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

Opens a ready-to-send draft in your own email app — review before sending.

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Eligibility criteria

Inclusion

Participants with the ability to understand the requirements of the trial, provide written informed consent, and comply with the trial protocol procedures.
Male or female participants aged ≥ 18 years.
Participants with diagnosis of GD who are hyperthyroid despite ATD treatment.

Exclusion

Have previously been successfully treated with radioactive iodine (RAI) therapy or have undergone total thyroidectomy.
Have an autoimmune disease other than GD requiring treatment that, in the Investigator's judgment, puts the participant at undue risk.
Have moderate-to-severe active 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.
  • Percentage of participants who are euthyroid and off ATD at Week 26 (Dose 1)Week 26