drugset / Trial / NCT01269242

The Effects of Bindarit in Preventing Stent Restenosis

NCT01269242 ↗

Phase 2 Completed 148 enrolled Angelini Pharma
RandomizedParallel-groupTriple-blindPrevention

Summary

The main study objective is to assess the efficacy and safety of different bindarit dosages compared to placebo in preventing restenosis, in patients submitted to coronary stenting and using a bare metal stent (Vision BMS, by Abbott).

Timeline

Start
2009-01
Primary completion
2011-01
Completion
2011-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Bindarit Small molecule 600 mg —
Subject Bindarit Small molecule 1200 mg —

Indications