deltatrials
Enrolling By Invitation INTERVENTIONAL NCT07286006

A Long-Term Extension Study of IMVT-1402 in Adult Participants With Graves' Disease (GD)

A Long-Term Extension Study to Assess the Efficacy, Safety, and Tolerability of IMVT-1402 in Adult Patients With Graves' Disease

Sponsor: Immunovant Sciences GmbH

Interventions IMVT-1402
Updated 3 times since 2026 Last updated: Apr 24, 2026 Started: Jan 26, 2026 Primary completion: Mar 1, 2030 Completion: Mar 1, 2030
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

Listed as NCT07286006, this observational or N/A phase trial focuses on Graves' Disease and remains ongoing. Sponsored by Immunovant Sciences GmbH, it has been updated 3 times since 2026, reflecting limited change activity. This study adds to the evidence base for this therapeutic area through structured, versioned documentation.

Status Flow

~Jan 2026 – ~Feb 2026 · 31 days · monthly snapshotNot Yet Recruiting~Feb 2026 – ~Apr 2026 · 3 months · monthly snapshotEnrolling By InvitationApr 28, 2026 – present · 3 months · daily APIEnrolling By Invitation

Change History

3 versions recorded
  1. Apr 28, 2026 — Present [daily]

    Enrolling By Invitation

    Phase: PHASE2None

  2. Feb 2026 — Apr 2026 [monthly]

    Enrolling By Invitation PHASE2

    Status: Not Yet RecruitingEnrolling By Invitation

  3. Jan 2026 — Feb 2026 [monthly]

    Not Yet Recruiting PHASE2

    First recorded

Eligibility Summary

This is a long-term extension study that will rollover participants completing feeder studies IMVT-1402-2502 (NCT06727604) or IMVT-1402-2503 (NCT07018323) to evaluate the efficacy and safety of IMVT-1402 in adult participants with GD. Eligible participants will be assigned to 1 of 3 study groups (Groups A, B and C) based on their GD status at the completion of their respective feeder study.

Contact Information

Sponsor contact:
  • Immunovant Sciences GmbH
Data source: ClinicalTrials.gov

For direct contact, visit the study record on ClinicalTrials.gov .