Phase 2 Dose-finding IMU-838 for Ulcerative Colitis
Trial details
- Registry ID
- NCT03341962
- Phase
- Phase 2
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Drug identity checked against registry records
Also recorded as IM90838; Vidofludimus calcium; vidofludimus calcium
| Trial | Sponsor | Phase | Status | Primary completion |
|---|---|---|---|---|
| Phase 2 Dose-finding IMU-838 for Ulcerative ColitisNCT03341962 | Immunic AG | Phase 2 | Terminated | 2022-11-16Actual |
| A Study to Evaluate the Efficacy, Safety and Tolerability of IMU-838 as Addition to Investigator's Choice of Standard of Care Therapy, in Patients With Coronavirus Disease 19 (COVID-19)NCT04379271 | Immunic AG | Phase 2, Phase 3 | Completed | 2021-01-12Actual |
| Study to Evaluate Efficacy, Safety, and Tolerability of IMU-838 in Patients With Progressive Multiple SclerosisNCT05054140 | Immunic AG | Phase 2 | Unknown | 2025-01-07Estimated |
| No regulatory events match this view.Try another date range or view. Events appear after automated source checks. This does not mean no FDA events have occurred. Dates that a source does not disclose stay undisclosed. |