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Enrolling By InvitationNCT07286006

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

Status
Enrolling By Invitation
Phase
Phase 2
Study type
Interventional
Enrollment
372 (estimated)
Sponsor
Immunovant Sciences GmbH · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGIMVT-1402Dose 1 for up to 52 weeks

Timeline

Start date
2026-01-26
Primary completion
2030-03-01
Completion
2030-03-01
First posted
2025-12-16
Last updated
2026-03-30

Locations

89 sites across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT07286006. Inclusion in this directory is not an endorsement.

A Long-Term Extension Study of IMVT-1402 in Adult Participants With Graves' Disease (GD) (NCT07286006) · Clinical Trials Directory