Effects of Vadadustat on Anemia, Quality of Life, and Inflammation in Dialysis Patients
Starting soon · Phase 4
Conditions studied: Renal Anemia
In brief
This is a two-period, two-sequence crossover study in patients receiving maintenance peritoneal dialysis. All participants remain on background darbepoetin alfa therapy throughout the study. The study compares add-on vadadustat plus background darbepoetin alfa with background darbepoetin alfa alone, with each treatment period lasting 8 weeks and separated by a 4-week washout period. Monthly laboratory assessments and dialysis adequacy measurements will be performed to evaluate anemia control, quality of life, inflammation, and dialysis adequacy.
Key facts
- Study ID
- NCT07537816
- Run by
- Mackay Memorial Hospital
- People needed
- 40
- Starts
- 2026-04-15
- Expected to finish
- 2026-10-15
- Last updated by the study team
- 2026-04-23
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age 18 years or older
- Receiving maintenance peritoneal dialysis
- Followed at the outpatient clinics of MacKay Memorial Hospital
- Receiving background darbepoetin alfa therapy
- Able and willing to provide informed consent
You may not qualify if…
- Blood pressure >170/80 mmHg on three separate occasions
- Recent cardiovascular events within the past 3 months, including coronary artery disease, myocardial ischemia, cerebrovascular disease, or peripheral artery disease
- Gastrointestinal bleeding within the past 3 months
- Active malignancy
Full record on ClinicalTrials.gov
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