drugset / Trial / NCT05327855
Efficacy and Safety of OPL-0301 Compared to Placebo in Adults With Post-Myocardial Infarction (MI)
RandomizedParallel-groupQuadruple-blindTreatment
Summary
Study OPL-0301-201 is intended to generate efficacy and safety data of OPL-0301 in participants with post-myocardial infarction (MI) left ventricular dysfunction (LVD)
Timeline
- Start
- 2022-09
- Primary completion
- 2024-08
- Completion
- 2024-11
Outcome
Outcome not reported
Stopped (Enrollment): “Withdrawn based on business decision, no participants enrolled”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | OPL-0301 | Unknown | — | Oral |