New registry tracks Real-World use of kidney anemia drug
NCT ID NCT07346547
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study is a registry that will collect information from 384 adults with chronic kidney disease (CKD) and anemia who are taking or starting the drug daprodustat. The goal is to understand how the drug works in everyday medical practice, including its effects on hemoglobin levels and heart health. The study does not test a new treatment but observes real-world outcomes to improve care and guidelines.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 384 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 2026
An estimate. Start dates often move.
- Expected to finish
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May 2027
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
patients with Chronic Kidney Disease (CKD) anemia requiring anemia treatment
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adults ≥ 18 years 2. Diagnosed CKD-associated anemia Chronic Kidney Disease (CKD) diagnosed as per KDIGO criteria, including: CKD stages G3-G5 (based on eGFR) * Patients on hemodialysis (HD) or peritoneal dialysis (PD) * Post-kidney transplant patients with CKD 3. Receiving or initiating Daprodustat therapy (new start or switch therapy) 4. CKD stages 3-5, dialysis patients (HD/PD), or post-transplant with CKD anemia 5. Able and willing to provide informed consent Exclusion Criteria 1. Acute Kidney Injury (AKI) without underlying chronicity 2. Hematologic disorders not related to CKD (e.g hemolytic anemia, aplastic anemia) 3. Refusal or inability to provide consent 4. Current enrollment in an interventional trial that restricts real-world data collection 5. Life expectancy \< 3 months, where follow-up is not feasible 6. Known contraindications to Daprodustat as per local prescribing information
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The study's own enquiry address
This study publishes an address for enquiries. See it below .
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
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Contacts and locations
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Study contacts
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Contact
Email: •••••@•••••
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