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Phase 2 Study Evaluating Rapcabtagene Autoleucel in Participants With Diffuse Cutaneous Systemic Sclerosis
The purpose of this study is to evaluate the efficacy, safety and tolerability of rapcabtagene autoleucel (administered once following lymphodepletion) in participants with severe refractory diffuse cutaneous systemic sclerosis relative to rituximab.
Details
| Lead sponsor | Novartis Pharmaceuticals |
|---|---|
| Phase | PHASE2 |
| Status | RECRUITING |
| Enrolment | 96 |
| Start date | Tue Oct 29 2024 00:00:00 GMT+0000 (Coordinated Universal Time) |
| Completion | Mon Aug 30 2032 00:00:00 GMT+0000 (Coordinated Universal Time) |
Conditions
- Scleroderma, Diffuse
Interventions
- rapcabtagene autoleucel
- rituximab
Countries
Brazil, Israel, France, Czechia, Germany, United States, Italy, Taiwan, Hungary, South Korea, Singapore, Switzerland, Austria, Spain, Denmark, Australia, Netherlands, United Kingdom, Japan, Belgium