drugset / Trial / NCT02769611

Ruboxistaurin in New York Heart Failure Classification III-IV Patients

NCT02769611 ↗

Non-randomizedParallel-groupOpen-labelTreatment

Summary

This study evaluates the effect of ruboxistaurin for its safety, tolerability, and effectiveness in treating adult patients with heart failure. Patients will receive 1 dose of oral ruboxistaurin.

Timeline

Start
2017-06-28
Primary completion
2022-01-01
Completion
2022-01-01

Outcome

Outcome not reported

Stopped (Business): “No funding”

Drugs

EvaluationDrugModalityDoseRoute
Subject Ruboxistaurin Small molecule 64 mg Oral
Subject Ruboxistaurin Small molecule 128 mg Oral
Subject Ruboxistaurin Small molecule 256 mg Oral

Indications