drugset / Trial / NCT06598631

Efficacy and Safety of Volenrelaxin in Adults With Chronic Kidney Disease

NCT06598631 ↗

Phase 2 Withdrawn Eli Lilly and Company
RandomizedParallel-groupDouble-blindTreatment

Summary

The main purpose of this study is to investigate the efficacy and safety of Volenrelaxin in adults with Chronic Kidney Disease. The study will last about 24 weeks.

Timeline

Start
2024-10-09
Primary completion
2024-12-30
Completion
2024-12-30

Outcome

Outcome not reported

Stopped: “Study was terminated due to a lack of foreseeable clinical benefit in the proposed chronic kidney disease population, following the termination of a related heart failure study that demonstrated no benefit in an overlapping patient group.”

Drugs

EvaluationDrugModalityDoseRoute
Subject Volenrelaxin Protein / enzyme biologic — Subcutaneous