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Completed Phase 2 Interventional Results available

4 Week Correction Study in Subjects With Anemia Associated With Chronic Kidney Disease Who Are Not Undergoing Dialysis

ClinicalTrials.gov ID: NCT01587898

Public ClinicalTrials.gov record NCT01587898. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 8:08 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Four-week Phase IIa, Randomized, Double-blind, Placebo-controlled, Parallel-group, Multi-center Study to Evaluate the Safety, Efficacy and Pharmacokinetics of GSK1278863 in Subjects With Anemia Associated With Chronic Kidney Disease Who Are Not Taking Recombinant Human Erythropoietin and Are Not Undergoing Dialysis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a four-week Phase IIa, randomized, double-blind, placebo-controlled, parallel-group, multi-center study to evaluate the safety, efficacy and pharmacokinetics of GSK1278863 in approximately 68 subjects with anemia associated with chronic kidney disease who are not taking rhEPO and are not undergoing dialysis. The range of Hgb values for study eligibility is 8.5-11.0 g/dL. Eligible subjects will be randomized in equal proportions to receive once daily (QD) placebo or GSK1278863 0.5 mg, 2 mg or 5 mg in a double-blind fashion.

Study identification

NCT ID
NCT01587898
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
72 participants

Conditions and interventions

Conditions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
18 Years to 99 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 17, 2012 (Actual)
Primary completion
May 7, 2013 (Actual)
Completion
May 7, 2013 (Actual)
Last update posted
Nov 9, 2017

2012 – 2013

United States locations

U.S. sites
46
U.S. states
13
U.S. cities
41
Facility City State ZIP Site status
GSK Investigational Site Azusa California 91702 —
GSK Investigational Site Bakersfield California 93309 —
GSK Investigational Site Chino California 91710 —
GSK Investigational Site Los Angeles California 90022 —
GSK Investigational Site Los Angeles California 90025 —
GSK Investigational Site Los Angeles California 90057 —
GSK Investigational Site North Hollywood California 91606-1559 —
GSK Investigational Site Orange California 92868 —
GSK Investigational Site Riverside California 92505 —
GSK Investigational Site San Dimas California 91773 —
GSK Investigational Site West Hills California 91307 —
GSK Investigational Site Yuba City California — —
GSK Investigational Site Denver Colorado 80230 —
GSK Investigational Site Daytona Beach Florida 32117 —
GSK Investigational Site Edgewater Florida 32132 —
GSK Investigational Site Fort Lauderdale Florida 33308 —
GSK Investigational Site Jacksonville Florida 32258 —
GSK Investigational Site Miami Florida 33145 —
GSK Investigational Site Miami Florida 33150 —
GSK Investigational Site Miami Florida 33173 —
GSK Investigational Site Ocala Florida 34471 —
GSK Investigational Site Pembroke Pines Florida 33028 —
GSK Investigational Site Port Charlotte Florida 33952 —
GSK Investigational Site Savannah Georgia 31406 —
GSK Investigational Site Evanston Illinois 60201 —
GSK Investigational Site Gurnee Illinois 60031 —
GSK Investigational Site Detroit Michigan 48236 —
GSK Investigational Site Asheville North Carolina 28801 —
GSK Investigational Site Charlotte North Carolina — —
GSK Investigational Site Wilmington North Carolina 28401 —
GSK Investigational Site Winston-Salem North Carolina 27103 —
GSK Investigational Site Columbus Ohio 43210 —
GSK Investigational Site Oklahoma City Oklahoma 73116 —
GSK Investigational Site Portland Oregon 97210 —
GSK Investigational Site Bethlehem Pennsylvania 18017 —
GSK Investigational Site Erie Pennsylvania 16507 —
GSK Investigational Site Uniontown Pennsylvania 15401 —
GSK Investigational Site Arlington Texas 76011 —
GSK Investigational Site Austin Texas 78751 —
GSK Investigational Site Corsicana Texas 75110 —
GSK Investigational Site Greenville Texas 75402 —
GSK Investigational Site Houston Texas 77054 —
GSK Investigational Site Houston Texas 77099 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site Temple Texas 76502 —
GSK Investigational Site Silverdale Washington 98383 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 9 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01587898, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 9, 2017 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01587898 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →