drugset / Trial / NCT05485818

Safety and Efficacy Study of Thymosin Beta 4 in Patients With Acute Myocardial Infarction.Infarction

NCT05485818 ↗

Phase 2 Completed 62 enrolled Beijing Northland Biotech. Co., Ltd.
RandomizedParallel-groupQuadruple-blindBasic science

Summary

A multicenter randomized double-blind placebo parallel control design was used in this study.60 subjects eligible for inclusion will be randomly assigned to either a low-dose (0.25ug/kg) medium-dose (0.5ug/kg) high-dose (2.0ug/kg) experimental drug group or a control group (placebo) at a ratio of 1:1:1:1.After randomization, subjects received the experimental drug or placebo once a day, intravenously, on day 2 to 7, 12 hours and 4 hours after PCI.Ninety days after PCI were observed.

Timeline

Start
2020-11-23
Primary completion
2021-09-30
Completion
2021-11-18

Drugs

EvaluationDrugModalityDoseRoute
Subject Thymosin β4 Protein / enzyme biologic 0.25 ug/kg Intravenous
Subject Thymosin β4 Protein / enzyme biologic 0.5 ug/kg Intravenous
Subject Thymosin β4 Protein / enzyme biologic 2 ug/kg Intravenous