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

PHASE2RecruitingINTERVENTIONAL
Enrollment

96

Participants

Timeline

Start Date

July 16, 2024

Primary Completion Date

December 21, 2025

Study Completion Date

December 21, 2025

Conditions
ST Elevation Myocardial Infarction
Interventions
DRUG

RTP-026

Intervention is for each subject administered as three 30-minutes infusions of either A: 25μg/kg RTP-026; or B: ≥ 26μg/kg and ≤75μg/kg RTP-026; or C: A maximum of 3 x treatment dose RTP-026 as given in B;

DRUG

Placebo

Intervention is for each subject administered as three 30-minutes infusions of placebo

Trial Locations (1)

2100

RECRUITING

Hjertecenteret, Rigshospitalet, Copenhagen

Sponsors

Lead Sponsor

All Listed Sponsors
lead

ResoTher Pharma

INDUSTRY

NCT06465303 - A Study of RTP-026 to Assess Safety, Tolerability and Efficacy in Patients With ST-Elevation Myocardial Infarction (STEMI) | Biotech Hunter | Biotech Hunter