Study to Evaluate the Efficacy, Safety and Pharmacokinetics of Three-times Weekly Dosing of GSK1278863 in Hemodialysis-dependent Subjects With Anemia Associated With Chronic Kidney Disease Who Are Switched From a Stable Dose of an Erythropoiesis-stimul…

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

A 29-DAY, RANDOMIZED, DOUBLE-BLINDED, PLACEBO-CONTROLLED, PARALLEL-GROUP, MULTI-CENTER STUDY TO EVALUATE THE EFFICACY, SAFETY AND PHARMACOKINETICS OF THREE-TIMES WEEKLY DOSING OF GSK1278863 IN HEMODIALYSIS-DEPENDENT SUBJECTS WITH ANEMIA ASSOCIATED WITH CHRONIC KIDNEY DISEASE WHO ARE SWITCHED FROM A STABLE DOSE OF AN ERYTHROPOIESIS-STIMULATING AGENT

Intervention/treatment:
GSK1278863
Medical condition:
KIDNEY DISEASE
Protocol code:
204836
Control number:
192517
Status:
Closed
Approved:
March 24, 2016
Date Completed:
Trial phase:
Phase 2
For more information:
ClinicalTrials.gov - NCT02689206
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
18 Years and older
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
GSK Response Center
Organization
GlaxoSmithKline
Phone:
866-435-7343
Sponsor
GLAXOSMITHKLINE INC

Locations

Alberta

GSK Investigational Site
Calgary, Alberta, T2R 0X7

Ontario

GSK Investigational Site
Ottawa, Ontario, K1H 7W9
GSK Investigational Site
Toronto, Ontario, M3M 0B2

Quebec

GSK Investigational Site
Greenfield Park, Quebec, J4V 2H1

Results

See the results from the trial NCT02689206. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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