drugset / Trial / NCT04320771

Study on the Safety of Neladenoson Bialanate, How it is Tolerated and the Way the Body Absorbs, Distributes and Gets Rid of the Study Dug Given as a Single Oral Dose of 10 mg Immediate Release Tablet in Participants With Renal Impairment and Healthy Participants Matched for Age-, Gender-, and Weight

NCT04320771 ↗

Phase 1 Terminated 18 enrolled Bayer
Non-randomizedParallel-groupOpen-labelBasic science

Summary

Neladenoson bialanate is currently under clinical development for a condition in which the heart has trouble pumping blood through the body (chronic heart failure). Renal impairment which co-occurs in patients with heart failure is a common condition in which the kidneys are not filtering the blood as well as they should. The goal of the study is to learn more about the safety of neladenoson bialanate, how it is tolerated and the way the body absorbs, distributes and excretes the study dug given as a single oral dose of 10 mg immediate release tablet in participants with renal impairment and healthy participants matched for age-, gender-, and weight

Timeline

Start
2017-11-02
Primary completion
2018-08-08
Completion
2018-12-17

Outcome

Outcome not reported

Stopped: “Termination of the development project for Neladenoson bialanate”

Drugs

EvaluationDrugModalityDoseRoute
Subject BAY1067197 Small molecule 10 mg Oral

Indications

No indication recorded.