drugset / Trial / NCT04616872

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

NCT04616872

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-inflammatory agent methotrexate in a cholesterol-rich non-protein nanoparticle (MTX-LDE) in patients with stable coronary disease. Patients with multi-vessels stable coronary disease will be randomized to receive MTX-LDE IV or placebo-LDE IV each 7 days for 12 weeks. The primary and main secondary endpoints will be analyzed by coronary and aortic CT angiography, that will be performed before the first treatment cycle, four weeks after the last drug infusion and 12 months after randomization. Patients will undergo clinical and laboratory safety evaluations before each treatment cycle, four weeks after the last cycle and 12 months after randomization. An algorithm for drug suspension based on clinical and laboratory finding will be followed.

Timeline

Start
2020-10-10
Primary completion
2022-10-12
Completion
2023-10-12

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Methotrexate Small molecule 40 mg/m2 Intravenous
Comparator folic acid Other / unclassified 5 mg Oral