drugset / Trial / NCT02976701

Effect of DLBS1033 After Primary PCI in Patients With STE-ACS

NCT02976701

Phase 2/3 Terminated 23 enrolled Dexa Medica Group Binawaluya Cardiac Hospital · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a prospective, randomized, double-blind, double-dummy, and controlled clinical study over a total of 4-week therapy with DLBS1033 in the management of STE-ACS after a primary PCI. There will be 40 STE-ACS subjects (20 subjects in each group) planned to complete the study.

Timeline

Start
2016-11
Primary completion
2023-01
Completion
2023-03

Drugs

EvaluationDrugModalityDoseRoute
Subject DLBS1033 Protein / enzyme biologic 980 mg
Background Aspirin Small molecule 80 mg
Background Clopidogrel Small molecule 75 mg