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Last Updated: December 22, 2024

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CLINICAL TRIALS PROFILE FOR VELPHORO


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All Clinical Trials for velphoro

Trial ID Title Status Sponsor Phase Start Date Summary
NCT02687594 ↗ Non-interventional Study to Investigate the Short and Long Term Real-life Safety, Effectiveness, and Adherence of Velphoro® in Patients With Hyperphosphataemia Undergoing Haemodialysis (HD) or Peritoneal Dialysis (PD) Completed Vifor Fresenius Medical Care Renal Pharma 2016-04-06 An oral highly potent P binder Velphoro is a mixture of polynuclear iron(III) oxyhydroxide, sucrose, and starches. It was well tolerated in the clinical development program. The approved indication in the European Union (EU) is to control serums phosphorus (sP) levels in adult CKD (Chronic kidney disease) patients on HD (Haemodialysis) or PD (Peritoneal dialysis). It is of major interest to observe the drug in daily use outside of controlled trial settings. The Marketing Authorisation Holder wishes to obtain further systematic data within a non-interventional study to investigate short and long-term safety. Effectiveness and Treatment adherence during real-life use will be evaluated.
NCT02688764 ↗ A Study to Investigate the Safety and Efficacy of PA21 (Velphoro®) and Calcium Acetate (Phoslyra®) in Paediatric and Adolescent Chronic Kidney Disease (CKD) Patients With Hyperphosphataemia Terminated Vifor Fresenius Medical Care Renal Pharma Phase 3 2016-05-26 This is a Phase 3, Open-label, Randomised, Active-controlled, Parallel Group, Multicentre Study to Investigate the Safety and Efficacy of PA21 (Velphoro®) and Calcium Acetate (Phoslyra®) in Paediatric and Adolescent CKD Patients with Hyperphosphataemia. The aim of this Phase 3 clinical study is to demonstrate similar efficacy of PA21 (Velphoro) in paediatric and adolescent patients with CKD, and to provide safety and dosing information for this patient population. The Phoslyra (comparator) group provides information for a descriptive comparison of PA21 against a commonly used calcium-based phosphate binder (calcium acetate).
NCT03010072 ↗ The Effect of Phosphate Lowering Using Sucroferric Oxyhydroxide (PA21) on Calcification Propensity of Serum Completed Vifor Fresenius Medical Care Renal Pharma Phase 2 2017-06-09 This is a single-center, prospective, open-label, controlled, randomized, cross-over study in 34 prevalent end-stage renal disease patients on chronic hemodialysis treatment with hyperphosphatemia.
NCT03010072 ↗ The Effect of Phosphate Lowering Using Sucroferric Oxyhydroxide (PA21) on Calcification Propensity of Serum Completed Prim. Priv. Doz. Dr. Daniel Cejka Phase 2 2017-06-09 This is a single-center, prospective, open-label, controlled, randomized, cross-over study in 34 prevalent end-stage renal disease patients on chronic hemodialysis treatment with hyperphosphatemia.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for velphoro

Condition Name

Condition Name for velphoro
Intervention Trials
Hyperphosphatemia 3
Endstage Renal Disease 1
Hypoalbuminemia 1
Peritoneal Dialysis Complication 1
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Condition MeSH

Condition MeSH for velphoro
Intervention Trials
Hyperphosphatemia 3
Hypoalbuminemia 1
Renal Insufficiency, Chronic 1
Kidney Failure, Chronic 1
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Clinical Trial Locations for velphoro

Trials by Country

Trials by Country for velphoro
Location Trials
United States 18
Germany 2
France 2
Netherlands 1
Lithuania 1
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Trials by US State

Trials by US State for velphoro
Location Trials
Oklahoma 1
North Carolina 1
New York 1
New Mexico 1
New Jersey 1
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Clinical Trial Progress for velphoro

Clinical Trial Phase

Clinical Trial Phase for velphoro
Clinical Trial Phase Trials
Phase 4 1
Phase 3 1
Phase 2 1
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Clinical Trial Status

Clinical Trial Status for velphoro
Clinical Trial Phase Trials
Completed 3
Terminated 1
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Clinical Trial Sponsors for velphoro

Sponsor Name

Sponsor Name for velphoro
Sponsor Trials
Vifor Fresenius Medical Care Renal Pharma 3
Prim. Priv. Doz. Dr. Daniel Cejka 1
University of Colorado, Denver 1
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Sponsor Type

Sponsor Type for velphoro
Sponsor Trials
Industry 3
Other 2
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