drugset / Trial / NCT02837237

Safety, Tolerability, and Pharmacokinetics of KBP-5074 Following Oral Administration in Chronic Kidney Disease

NCT02837237 ↗

Phase 1 Completed 11 enrolled KBP Biosciences
NaSingle-groupOpen-labelTreatment

Summary

This study explores the use of KBP-5074 in patients with advanced stages of Chronic Kidney Disease (CKD) (including patients with severe renal impairment and those on hemodialysis \[HD\]) and to assess the safety, tolerability, and pharmacokinetics (PK) of single doses of KBP-5074 in male and female patients with severe CKD (defined as estimated glomerular filtration rate \[eGFR\] ≥15 mL/min/1.73 m2 and ≤29 mL/min/1.73 m2, based on the Modification of Diet in Renal Disease \[MDRD\] equation) and a subset of patients requiring HD.

Timeline

Start
2016-07-13
Primary completion
2016-12-20
Completion
2017-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Ocedurenone Small molecule — Oral