A Phase 2, Multicenter, Double-blind, Two-arm Study of Subcutaneous RO7790121 for the Treatment of Subjects With Moderate to Severe Active Crohn's Disease
Latest Information Update: 07 Oct 2024
At a glance
- Drugs RVT-3101 (Primary)
- Indications Crohn's disease
- Focus Adverse reactions
- Acronyms TAHOE
- Sponsors Roche; Roivant Sciences
Most Recent Events
- 27 Sep 2024 Trial focus changed from TU to AR. Primary endpoint ' Proportion of participants achieving clinical remission by CDAI Induction of Clinical Remission by CDAI [Time Frame: Week 14]' to 'Incidence of Treatment-Emergent Adverse Events (TEAE), Serious Adverse Events (SAE) and AE Leading to Discontinuation time-frame: Until end of study, approximately 5 years'.
- 27 Sep 2024 Planned End Date changed from 15 Dec 2025 to 31 Dec 2030.
- 27 Sep 2024 Planned End Date changed from 15 Dec 2025 to 31 Dec 2030.