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

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-79
SponsorBeijing Sungen Biomedical Technology Co., Ltd

About this trial

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).

Eligibility criteria

Qualifiers

None

Disqualifiers

History of myocardial infarction, coronary revascularization (including percutaneous coronary intervention [PCI] and coronary artery bypass grafting [CABG], etc.);

History of cardiopulmonary resuscitation;

History of stroke within 6 months;

Presence of severe cardiac structural abnormalities such as aortic dissection, and ventricular aneurysm;

Trial design

Treatments tested in this trial

  • SGC001 injection
  • SGC001 injection
  • Placebo

Treatment groups

210 Participants
are divided into 3 treatment groups