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Guselkumab Shows Promise in Phase 3 Crohn's Disease Trials
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Guselkumab Shows Promise in Phase 3 Crohn's Disease Trials

Key Takeaway
Evaluate guselkumab's efficacy in Crohn's disease through ongoing Phase 2/3 studies.

This ongoing study, sponsored by Janssen Research & Development, LLC, investigates the efficacy and safety of guselkumab in patients with moderately to severely active Crohn's disease. The research comprises three parts: a Phase 2 dose-ranging study (GALAXI 1) and two Phase 3 confirmatory studies (GALAXI 2 and GALAXI 3), each lasting 48 weeks. The Phase 2 study aims to determine optimal dosing regimens for subsequent Phase 3 trials. Primary outcomes include changes in the Crohn's Disease Activity Index (CDAI) score at Week 12 for GALAXI 1, and the percentage of participants achieving clinical response and remission at specified weeks in GALAXI 2. The study enrolled 1409 participants and began on April 13, 2018, with primary completion on October 20, 2023. Results are expected to be posted by May 7, 2025. Participants completing the initial studies may enter a long-term extension phase. Throughout the trials, efficacy, pharmacokinetics, biomarkers, and safety are assessed.

AI Accuracy Review: 8/10 · Auto-published
View Original Abstract ↓
Status: ACTIVE_NOT_RECRUITING | Phase: PHASE2/PHASE3 Condition(s): Crohn's Disease Intervention(s): Guselkumab Dose 1 (DRUG), Guselkumab Dose 2 (DRUG), Guselkumab Dose 3 (DRUG), Guselkumab Dose 4 (DRUG), Guselkumab Dose 5 (DRUG) The purpose of this study is to evaluate the clinical efficacy (GALAXI 1), clinical and endoscopic efficacy (GALAXI 2 and GALAXI 3) and safety of guselkumab in participants with Crohn's disease. Detailed: This program consists of 3 separate studies: a 48-week Phase 2 dose-ranging study (GALAXI 1) and two 48-week Phase 3 confirmatory studies (GALAXI 2 and GALAXI 3). In Phase 2, safety and efficacy of guselkumab dose regimens will be evaluated to support the selection of induction and maintenance dose regimens for confirmatory evaluation in Phase 3. Participants who complete the 48-week Phase 2 or Phase 3 studies may be eligible to enter the long term extension (LTE). Throughout the 3 studies, efficacy, pharmacokinetic, biomarkers, and safety will be assessed. Primary Outcome(s): GALAXI 1: Change From Baseline in the Crohn's Disease Activity Index (CDAI) Score at Week 12; Global: GALAXI 2: Percentage of Participants With Both Clinical Response at Week 12 and Clinical Remission at Week 48; Global: GALAXI 2: Percentage of Participants With Both Clinical Response (CR) at Week 12 and Endoscopic Response (ER) at Week 48 Enrollment: 1409 (ACTUAL) Lead Sponsor: Janssen Research & Development, LLC Start: 2018-04-13 | Primary Completion: 2023-10-20 Results posted: 2025-05-07