Trial Profile

A Phase 2b, Multicenter, Double-blind, Placebo-controlled Randomized Withdrawal Study to Assess the Efficacy, Safety, and Tolerability of IMVT-1402 in Adult Participants With Active, Difficult to Treat, ACPA-Positive Rheumatoid Arthritis

Status: Active, no longer recruiting

Phase of Trial: Phase II

Latest Information Update: 20 Aug 2026

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At a glance

20 Jul 2026 Planned number of patients changed from 291 to 185.
01 Jun 2026 New source identified and integrated(Clinical Trials Information System)
20 May 2026 According to a Immunovant media release, a total of 170 participants have been enrolled in the initial 16-week open label period (Period 1) of the study evaluating weekly subcutaneous (SC) dosing of IMVT-1402 600 mg and at completion, 165 of 170 patients were evaluable for ACR20 response.

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