Safety, Tolerability, PK Profile, and Symptom Response of a 7-Day Dosing With 25 mg or 50 mg Daily of REL-1017 in MDD
Trial details
- Registry ID
- NCT03051256
- Phase
- Phase 2
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Research sample: selected versions from May 2023 onward plus a preceding baseline where available. Only selected fields were retained; endpoint measures were truncated to 300 characters. This is not complete trial or sponsor history. Daily snapshots begin when collection starts.
| Trial | Sponsor | Phase | Status | Primary completion |
|---|---|---|---|---|
| Safety, Tolerability, PK Profile, and Symptom Response of a 7-Day Dosing With 25 mg or 50 mg Daily of REL-1017 in MDDNCT03051256 | RLMD | Phase 2 | Completed | 2019-07-30Actual |
| A Study to Assess the Efficacy and Safety of REL-1017 as Adjunctive Treatment for Major Depressive Disorder (MDD)NCT04688164 | RLMD | Phase 3 | Completed | 2022-11-01Actual |
| Safety of REL-1017 for Major Depressive DisorderNCT04855760 | RLMD | Phase 3 | Completed | 2023-07-27Actual |
| A Study to Assess the Efficacy and Safety of REL-1017 as Monotherapy for Major Depressive Disorder (MDD)NCT05081167 | RLMD | Phase 3 | Completed | 2022-09-13Actual |
| A Study to Evaluate the Safety and Efficacy of NDV-01 in Participants With NMIBCNCT06663137 | RLMD | Phase 2 | Recruiting | 2027-11Estimated |
| A Study of NDV-01 (Sustained-release Gemcitabine-docetaxel) in Participants With Non-muscle Invasive Bladder CancerNCT07464145 | RLMD | Phase 3 | Not yet recruiting | 2029-12Estimated |
NCT06663137 · Relmada Therapeutics, Inc.
Aug 2025
Nov 2027
NCT07464145 · Relmada Therapeutics, Inc.
Sep 2029
Dec 2029