drugset / Trial / NCT04148833

Treatment of Patients With Atherosclerotic Disease With Paclitaxel-associated to LDL Like Nanoparticles

NCT04148833

Phase 2/3 Unknown 40 enrolled University of Sao Paulo General Hospital
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The investigators propose a prospective, randomized, double-blind, placebo-controlled study. The purpose of the study is to evaluate the safety and efficacy of an anti-proliferative agent paclitaxel in a cholesterol-rich non-protein nanoparticle (Paclitaxel -LDE) in patients with stable coronary disease. Patients with multi-vessels stable coronary disease will be randomized to receive Paclitaxel-LDE IV or placebo-LDE IV each 21 days for 6 weeks. The primary and main secondary endpoints will be analyzed by coronary and aortic CTA, that will be performed 1-4 weeks after randomization and at 3-8 weeks after the last treatment cycle. Patients will undergo clinical and laboratory safety evaluations before each treatment cycle and 3-8 weeks after the last cycle. An algorithm for drug suspension based on clinical and laboratory finding will be followed.

Timeline

Start
2019-06-23
Primary completion
2020-08-12
Completion
2021-08-23

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Paclitaxel Small molecule 175 mg/m2 Intravenous