Clinical Trials Directory

Trials / Completed

CompletedNCT02829320

Efficacy and Safety Study of GSK1278863 in Japanese Hemodialysis Subjects With Anemia Associated With Chronic Kidney Disease Who Are Not Taking Erythropoiesis Stimulating Agents

A 24-week, Phase III, Open-label, Non-comparative, Multi-center Study to Evaluate Efficacy and Safety of GSK1278863 in Japanese Hemodialysis Subjects With Anemia Associated With Chronic Kidney Disease Who Are Not Taking Erythropoiesis Stimulating Agents

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
28 (actual)
Sponsor
GlaxoSmithKline · Industry
Sex
All
Age
20 Years
Healthy volunteers
Not accepted

Summary

This 24-week, Phase 3, open-label, non-comparative, multicentre study aims to evaluate the efficacy and safety of GSK1278863 in Japanese hemodialysis (HD) patients with renal anemia not using erythropoiesis-stimulating agents (ESAs). The primary objective is to evaluate the initial response to GSK1278863 measured by hemoglobin (Hgb) levels in HD patients not using ESAs enrolled in this study. The study is designed to evaluate the appropriateness of the starting dose of GSK1278863 and of the GSK1278863 dose adjustment regimen to achieve or maintain the target Hgb levels. This study will consist of a 4-week screening period, a 24-week treatment period (4-week fixed-dose period and a 20-week dose adjustment period), and a 2- to 4-week follow-up period.

Conditions

Interventions

TypeNameDescription
DRUGGSK1278863GSK1278863 will be provided as round, standard biconvex, white film coated tablets containing 1 mg, 2 mg, 4 mg or 6 mg of GSK1278863 as active ingredient.
DRUGIronSubjects will receive supplemental iron therapy if ferritin is \<=100 ng/mL and TSAT is \<=20%. The investigator (or subinvestigator) will choose the route of administration and dose of prescription iron.

Timeline

Start date
2016-08-08
Primary completion
2017-05-16
Completion
2017-10-17
First posted
2016-07-12
Last updated
2019-12-03
Results posted
2018-07-13

Locations

17 sites across 1 country: Japan

Source: ClinicalTrials.gov record NCT02829320. Inclusion in this directory is not an endorsement.