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Completed Phase 3 Interventional Results available

Anemia Studies in Chronic Kidney Disease (CKD): Erythropoiesis Via a Novel Prolyl Hydroxylase Inhibitor (PHI) Daprodustat in Non-Dialysis Subjects Evaluating Hemoglobin (Hgb) and Quality of Life (ASCEND-NHQ)

ClinicalTrials.gov ID: NCT03409107

Public ClinicalTrials.gov record NCT03409107. 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, 7:36 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 28-week, Randomized, Double-blind, Placebo-controlled, Parallel-group, Multi-center, Study in Recombinant Human Erythropoietin (rhEPO) naïve Non-dialysis Participants With Anemia Associated With Chronic Kidney Disease to Evaluate the Efficacy, Safety and Effects on Quality of Life of Daprodustat Compared to Placebo

Brief summary

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

The purpose of this multi-center study in non-dialysis participants with anemia associated with CKD is to evaluate safety, efficacy and quality of life of daprodustat compared to placebo.

Study identification

NCT ID
NCT03409107
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
614 participants

Conditions and interventions

Conditions

Eligibility (public fields only)

Age range
18 Years and older
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
Mar 5, 2018 (Actual)
Primary completion
Oct 7, 2020 (Actual)
Completion
Oct 7, 2020 (Actual)
Last update posted
Apr 2, 2024

2018 – 2020

United States locations

U.S. sites
49
U.S. states
20
U.S. cities
47
Facility City State ZIP Site status
GSK Investigational Site Homewood Alabama 35209 —
GSK Investigational Site Little Rock Arkansas 72204 —
GSK Investigational Site Downey California 90242 —
GSK Investigational Site Fresno California 93720 —
GSK Investigational Site Lynwood California 90262 —
GSK Investigational Site Northridge California 91324 —
GSK Investigational Site Northridge California 91325 —
GSK Investigational Site Riverside California 82503 —
GSK Investigational Site Salinas California 93901 —
GSK Investigational Site Santa Ana California 92704 —
GSK Investigational Site Denver Colorado 80230 —
GSK Investigational Site Hartford Connecticut 06112 —
GSK Investigational Site Middlebury Connecticut 06762 —
GSK Investigational Site Coral Springs Florida 33067 —
GSK Investigational Site Hollywood Florida 33024 —
GSK Investigational Site Kissimmee Florida 34741 —
GSK Investigational Site Lauderdale Lakes Florida 33313 —
GSK Investigational Site Pembroke Pines Florida 33028 —
GSK Investigational Site Tampa Florida 33614 —
GSK Investigational Site Adairsville Georgia 30103 —
GSK Investigational Site Macon Georgia 31201 —
GSK Investigational Site Macon Georgia 31217 —
GSK Investigational Site Statesboro Georgia 30458 —
GSK Investigational Site Indianapolis Indiana 46260 —
GSK Investigational Site Overland Park Kansas 66210 —
GSK Investigational Site Buckley Michigan 49620 —
GSK Investigational Site Detroit Michigan 48202 —
GSK Investigational Site Saint Clair Shores Michigan 48081 —
GSK Investigational Site Brookhaven Mississippi 39601 —
GSK Investigational Site St Louis Missouri 63136 —
GSK Investigational Site Rochester New Hampshire 03867 —
GSK Investigational Site Asheville North Carolina 28801 —
GSK Investigational Site Charlotte North Carolina 28262 —
GSK Investigational Site Durham North Carolina 27704 —
GSK Investigational Site Midwest City Oklahoma 73130 —
GSK Investigational Site Oklahoma City Oklahoma 73112 —
GSK Investigational Site Beaver Pennsylvania 15009 —
GSK Investigational Site Duncansville Pennsylvania 16635 —
GSK Investigational Site Scottdale Pennsylvania 15683 —
GSK Investigational Site Smithfield Pennsylvania 15478 —
GSK Investigational Site West Reading Pennsylvania 19611 —
GSK Investigational Site Orangeburg South Carolina 29118 —
GSK Investigational Site Kingsport Tennessee 37660 —
GSK Investigational Site Memphis Tennessee 38163 —
GSK Investigational Site DeSoto Texas 75115 —
GSK Investigational Site El Paso Texas 79935 —
GSK Investigational Site McAllen Texas 78503 —
GSK Investigational Site Waxahachie Texas 75165 —
GSK Investigational Site Norfolk Virginia 23502 —

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 119 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03409107, 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 Apr 2, 2024 · 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 NCT03409107 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →