drugset / Trial / NCT05327855

Efficacy and Safety of OPL-0301 Compared to Placebo in Adults With Post-Myocardial Infarction (MI)

NCT05327855 ↗

Phase 2 Withdrawn Valo Health, Inc.
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Stopped (Enrollment): “Withdrawn based on business decision, no participants enrolled”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

EvaluationDrugModalityDoseRoute
Subject OPL-0301 Unknown — Oral

Indications