imeroprubart (IMVT-1402) - Immunovant, HanAll Biopharma
Preliminary Results from IMVT-1402 Trial in D2T RA (The Manila Times) - May 20, 2026 - "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...Baseline disease activity was high, with mean counts of 24.2 tender joints, 16.7 swollen joints, and a DAS28-CRP score of 6.1. At Week 16, the observed ACR20, ACR50, and ACR70 response rates were 72.7%, 54.5%, and 35.8%, respectively; participants who discontinued prior to Week 16 were imputed as non-responders. Among the subset of participants who had failed at least a JAK inhibitor and an anti-TNF inhibitor (N=107), the Week 16 observed ACR20, ACR50 and ACR70 response rates were 72.0%, 53.3% and 37.4%, respectively....We anticipate providing further updates on this program in the second half of calendar year 2026." 
P2 data • Trial status • Rheumatoid Arthritis
https://www.manilatimes.net/2026/05/20/tmt-newswire/globenewswire/roivant-reports-financial-results-for-the-fourth-quarter-and-fiscal-year-ended-march-31-2026-and-provides-business-update/2348063/amp
 
May 20, 2026
 
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