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ClinicalTrials.gov record
Active, not recruiting Phase 3 Interventional

To Evaluate the Efficacy of Three Times Weekly (TIW) Vadadustat Compared to Standard of Care ESA in Patients With Anemia of CKD Receiving In-Center Hemodialysis

ClinicalTrials.gov ID: NCT06901505

Public ClinicalTrials.gov record NCT06901505. 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 May 19, 2026, 11:21 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 Randomized, Open-Label, Active-Controlled Study Evaluating the Efficacy of Three Times Weekly Vadadustat Compared to Standard of Care ESA in Patients With Anemia of CKD Receiving In-Center Hemodialysis

Study identification

NCT ID
NCT06901505
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Akebia Therapeutics
Industry
Enrollment
353 participants

Conditions and interventions

Interventions

  • Erythropoiesis-Stimulating Agent (ESA) Drug
  • Vadadustat Drug

Drug

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
Jul 23, 2025
Primary completion
Jul 31, 2026
Completion
Jul 31, 2026
Last update posted
Feb 22, 2026

2025 – 2026

United States locations

U.S. sites
18
U.S. states
7
U.S. cities
12
Facility City State ZIP Site status
DaVita Research Site Montgomery Alabama 36117-7306
DaVita Research Site Hartford Connecticut 06112-1260
DaVita Research Site Middlebury Connecticut 06705-3893
DaVita Research Site Columbus Georgia 31904-3604
DaVita Research Site #1 Minneapolis Minnesota 55435-1807
DaVita Research Site Minneapolis Minnesota 55435-1807
DaVita Research Site Henderson Nevada 89052-5548
DaVita Research Site Las Vegas Nevada 89128-0804
DaVita Research Site #1 El Paso Texas 79835-2200
DaVita Research Site El Paso Texas 79835-2200
DaVita Research Site #1 Houston Texas 77054-3836
DaVita Research Site Houston Texas 77054-3836
DaVita Research Site #1 San Antonio Texas 78258-4800
DaVita Research Site #2 San Antonio Texas 78258-4800
DaVita Research Site San Antonio Texas 78258-4800
DaVita Research Site The Woodlands Texas 77384-3024
DaVita Research Site #1 Norfolk Virginia 23502-3235
DaVita Research Site Norfolk Virginia 23502-3235

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06901505, 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 Feb 22, 2026 · Synced May 19, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06901505 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →