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

PHASE1CompletedINTERVENTIONAL
Enrollment

11

Participants

Timeline

Start Date

July 13, 2016

Primary Completion Date

December 20, 2016

Study Completion Date

June 30, 2017

Conditions
Chronic Kidney Disease
Interventions
DRUG

KBP-5074

"In Part 1 of the study, non-HD patients with severe CKD in Cohort 1 will receive a single oral capsule dose of KBP-5074 on Day 1 following a fast between 2 and 4 hours.~In Part 2 of the study, HD patients with severe CKD will receive a single oral capsule dose of KBP-5074 following a fast between 2 and 4 hours. The dose of KBP 5074 will be administered on Day 1 immediately following a dialysis session."

Trial Locations (1)

08540

KBP Biosciences USA Inc, Princeton

Sponsors

Lead Sponsor

All Listed Sponsors
lead

KBP Biosciences

INDUSTRY