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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 Incident Dialysis (ASCEND-ID)

ClinicalTrials.gov ID: NCT03029208

Public ClinicalTrials.gov record NCT03029208. 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 23, 2026, 4:49 AM 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 52-week Open-label (Sponsor-blind), Randomized, Active-controlled, Parallel-group, Multi-center Study to Evaluate the Efficacy and Safety of Daprodustat Compared to Recombinant Human Erythropoietin in Subjects With Anemia Associated With Chronic Kidney Disease Who Are Initiating Dialysis

Brief summary

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

The purpose of this multi-center study is to evaluate the efficacy and safety of daprodustat in subjects with anemia associated with CKD.

Study identification

NCT ID
NCT03029208
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
312 participants

Conditions and interventions

Conditions

Interventions

Drug

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 11, 2017 (Actual)
Primary completion
Sep 24, 2020 (Actual)
Completion
Sep 24, 2020 (Actual)
Last update posted
Oct 20, 2021

2017 – 2020

United States locations

U.S. sites
36
U.S. states
14
U.S. cities
34
Facility City State ZIP Site status
GSK Investigational Site Anaheim California 92801 —
GSK Investigational Site Cerritos California 90703 —
GSK Investigational Site Escondido California 92025 —
GSK Investigational Site Glendale California 91204 —
GSK Investigational Site La Palma California 90623 —
GSK Investigational Site Los Angeles California 90022 —
GSK Investigational Site Los Angeles California 90095 —
GSK Investigational Site Lynwood California 90262 —
GSK Investigational Site Sacramento California 95825 —
GSK Investigational Site Whittier California 90603 —
GSK Investigational Site Middlebury Connecticut 06762 —
GSK Investigational Site Coral Gables Florida 33134 —
GSK Investigational Site Miami Florida 33126 —
GSK Investigational Site Miami Florida 33169 —
GSK Investigational Site Augusta Georgia 30912 —
GSK Investigational Site Chicago Illinois 60637 —
GSK Investigational Site Crystal Lake Illinois 60014 —
GSK Investigational Site Fort Wayne Indiana 46804 —
GSK Investigational Site Merrillville Indiana 46410 —
GSK Investigational Site Michigan City Indiana 46360 —
GSK Investigational Site Iowa City Iowa 52242 —
GSK Investigational Site Baton Rouge Louisiana 70809 —
GSK Investigational Site New Orleans Louisiana 70112 —
GSK Investigational Site Baltimore Maryland 21287 —
GSK Investigational Site Jackson Mississippi 39216 —
GSK Investigational Site Kansas City Missouri 64111 —
GSK Investigational Site St Louis Missouri 63110 —
GSK Investigational Site Brooklyn New York 11203 —
GSK Investigational Site Buffalo New York 14215 —
GSK Investigational Site Mineola New York 11501 —
GSK Investigational Site New York New York 10029 —
GSK Investigational Site The Bronx New York 10461 —
GSK Investigational Site Houston Texas 77004 —
GSK Investigational Site Lufkin Texas 75904 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site Hampton Virginia 23666 —

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 75 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03029208, 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 Oct 20, 2021 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03029208 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →