drugset / Trial / NCT07306182

A Research Study to Evaluate the Efficacy and Safety of SGC001 in Patients With Anterior Wall ST-Segment Elevation Myocardial Infarction

NCT07306182 ↗

Phase 2 Recruiting 210 enrolled Beijing Sungen Biomedical Technology Co., Ltd
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a multicenter, randomized, double-blind, placebo-controlled, single-dose, Phase II clinical study to evaluate the efficacy, safety, and pharmacokinetic (PK) characteristics of SGC001 injection administered in addition to standard clinical care in Chinese patients with acute anterior ST-segment elevation myocardial infarction (STEMI) who are planned for primary percutaneous coronary intervention (pPCI).

Timeline

Start
2026-03-09
Primary completion
2027-04
Completion
2027-10

Drugs

EvaluationDrugModalityDoseRoute
Subject SGC001 Unknown 600 mg Intravenous
Subject SGC001 Unknown 900 mg Intravenous