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Clinical Trial ● Currently Recruiting Phase II NCT06727604

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

A Study to Assess the Efficacy, Safety, and Tolerability of IMVT-1402 as Treatment for Adult Participants With Graves’ Disease — Recruiting • Phase II • NCT06727604.

📅 22 Apr 2026 ⏱ 1 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Phase II
NCT ID
NCT06727604
Start
2024-12-17
Completion
2028-06
ClinicaliQ Trial Snapshot
  • A Study to Assess the Efficacy, Safety, and Tolerability of IMVT-1402 as Treatment for Adult Participants With Graves’ Disease — Recruiting • Phase II • NCT06727604.
  • New drug IMVT-1402 tested against placebo in adults with Graves' disease uncontrolled by standard thyroid medications.

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  • Quick orientation before opening the registry record.
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What This Trial Is Studying

This is a study to assess the efficacy, safety, and tolerability of IMVT-1402 in adult participants with Graves' disease (GD) who are hyperthyroid despite antithyroid drug (ATD) treatment. The primary objective of this study is to evaluate the efficacy of IMVT-1402 versus placebo as assessed by T3 (total triiodothyronine [T3] or free triiodothyronine [FT3]), free thyroxine (FT4), thyroid-stimulating hormone (TSH), and ATD dose at Week 26. Conditions: Graves' Disease Interventions: IMVT-1402, IMVT-1402, Placebo Lead Sponsor: Immunovant Sciences GmbH Planned Enrollment: 240 participants

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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