Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
Study of Phosphate Levels in Patients With Chronic Kidney Disease
NCT00824460 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to investigate the ability of different doses of PA21 to lower serum phosphate levels, in patients with chronic kidney disease on maintenance hemodialysis.
Conditions Studied
Interventions
- DRUG 1.25 g PA21 (250 mg iron)
- DRUG 5.0 g PA21 (1,000 mg iron)
- DRUG 7.5 g PA21 (1,500 mg iron)
- DRUG 10.0 g PA21 (2,000 mg iron)
- DRUG 12.5 g PA21 (2,500 mg iron)
Study Locations (20)
Other
- MHAT — Gabrovo
- MHAT Plovdiv — Plovdiv
- Department of Haemodialysis at MHAT — Rousse
- 5th MHAT Sofia — Sofia
- SHATCVD - National Cardiology Hospital — Sofia
- MHAT "Tokuda Hospital Sofia" — Sofia
- UMHAT "Alexandrovska" Dialysis Clinic — Sofia
- UMHAT "Sveti Ivan Rilski" — Sofia
- UMHAT "Sveta Anna" — Sofia
- MDHAT Department of Haemodialysis and Nephrology — Veliko Tarnovo
- Opca bonica Bjelovar — Bjelovar
Colorado
- Western Nephrology & Metabolic Disease — Arvada
- Complete Renal Care — Denver
Tennessee
- Southeast Renal Research Institute — Chattanooga
- Nephrology Associates — Nashville
Florida
- Pines Clinical Research — Pembroke Pines
Kansas
- University of Kansas Medical Center — Kansas City
New York
- Nephrology Associates — Fresh Meadows
Ohio
- University Hospitals / Case Medical Center — Cleveland
Texas
- Southwest Houston Research — Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 154 participants |
| Start Date | 2008-12 |
| Est. Completion | 2010-03 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00824460
The ClinicalTrials.gov registry entry for NCT00824460 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 154 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Vifor Pharma, which has 4 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Chronic Kidney Disease appearing as the primary indexed condition, and to 5 interventions — of which 1.25 g PA21 (250 mg iron) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT00824460 reports 20 study locations spanning 8 distinct geographic areas — top geographies include Other, Colorado, Tennessee. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT00824460 about?
NCT00824460 is a clinical study titled "Study of Phosphate Levels in Patients With Chronic Kidney Disease". The purpose of this study is to investigate the ability of different doses of PA21 to lower serum phosphate levels, in patients with chronic kidney disease on maintenance hemodialysis.
What is the current status of trial NCT00824460?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 154 participants. The study started on 2008-12. Estimated completion is 2010-03.
What conditions does trial NCT00824460 study?
This clinical trial studies the following conditions: Chronic Kidney Disease. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00824460?
The interventions under investigation include: 1.25 g PA21 (250 mg iron) (DRUG), 5.0 g PA21 (1,000 mg iron) (DRUG), 7.5 g PA21 (1,500 mg iron) (DRUG), 10.0 g PA21 (2,000 mg iron) (DRUG), 12.5 g PA21 (2,500 mg iron) (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00824460?
This trial is sponsored by Vifor Pharma, which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00824460 being conducted?
This trial has 20 study locations across Colorado, Florida, Kansas, New York, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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