drugset / Trial / NCT06465303

A Study of RTP-026 to Assess Safety, Tolerability and Efficacy in Patients With ST-Elevation Myocardial Infarction (STEMI)

NCT06465303 ↗

Phase 2 Recruiting 96 enrolled ResoTher Pharma
RandomizedParallel-groupTriple-blindTreatment

Summary

This is an exploratory, randomized, double-blind, multicentre, placebo-controlled study of RTP-026. The study population will consist of men and women with documented evidence of ST-elevation myocardial infarction (STEMI) referred to primary Percutaneous Coronary Intervention (PCI).

Timeline

Start
2024-07-16
Primary completion
2025-12-21
Completion
2025-12-21

Drugs

EvaluationDrugModalityDoseRoute
Subject RTP-026 Unknown 25 ug/kg Intravenous
Subject RTP-026 Unknown 26 ug/kg Intravenous
Subject RTP-026 Unknown 75 ug/kg Intravenous