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Abivax Announces Positive Phase 3 Results from Both ABTECT 8-Week Induction Trials Investigating Obefazimod, its First-in-Class Oral miR-124 Enhancer, in Moderate to Severely Active Ulcerative Colitis

Abivax Announces Positive Phase 3 Results from Both ABTECT 8-Week Induction Trials Investigating Obefazimod, its First-in-Class Oral miR-124 Enhancer, in Moderate to Severely Active Ulcerative Colitis 50 mg once-daily dose of obefazimod led to a compelling pooled 16.4% (p<0.0001) placebo-adjusted clinical remission rate at Week 8 in the ABTECT-1 (Study 105) and ABTECT-2 (Study 106) trials. Individually, the 50 mg dose demonstrated a placebo-adjusted remission rate of 19.3% (p<0.0001) in ABTECT-1

articleAbivax SaJuly 22, 20256/company/abivax-sa-1/news/abivax-announces-positive-phase-3-results-from-both-abtect-8-week-induction-trials-investigating-obefazimod-its-first-in-class-oral-mir-124-enhancer-in-moderate-to-severely-active-ulcerative-colitis
Abivax Announces Positive Phase 3 Results from Both ABTECT 8-Week Induction Trials Investigating Obefazimod, its First-in-Class Oral miR-124 Enhancer, in Moderate to Severely Active Ulcerative Colitis

About this update from Abivax Sa

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Ulcerative ColitisPhase 3 clinical trialsEuronext Paristopline resultsregulatory mechanismsbiotechnology companyadult patientsresponse rate