Safety and Efficacy of FAP iCDC in Acute Myocardial Infarction With Cardiogenic Shock

Trial statusNot yet recruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18-80
SponsorSecond Affiliated Hospital, School of Medicine, Zhejiang University

About this trial

To study the safety and efficacy of fibroblast activation protein (FAP)-targeted allogeneic immunosuppressive chimeric antigen receptor-dendritic cell (CAR-DC) in the treatment of acute myocardial infarction with cardiogenic shock and provide a new method for the treatment of acute myocardial infarction with cardiogenic shock.

Eligibility criteria

Qualifiers

Age ≥ 18 years and < 80 years.

Post-emergent revascularization (PCI or CABG)

Systolic blood pressure < 90 mmHg for >30 minutes, or requiring catecholamine support to maintain systolic blood pressure >90 mmHg

Altered mental status

Disqualifiers

Acute mechanical complications of infarction (e.g., ventricular septal rupture, acute mitral regurgitation).

Cardiac arrest.

Hypoxic-ischemic brain injury (cerebral injury with fixed and dilated pupils not attributable to medication).

Shock due to other causes (e.g., sepsis, hypovolemia).

Trial design

Treatments tested in this trial

  • FAP allogeneic immunosuppressive CAR-DC

Treatment groups

18 Participants
are divided into 2 treatment groups