drugset / Trial / NCT01521494

PA21 Phase II Clinical Study in Hemodialysis Patients With Hyperphosphatemia

NCT01521494

Phase 2 Completed 183 enrolled Kissei Pharmaceutical Co., Ltd.
RandomizedParallel-groupDouble-blindTreatment

Summary

To investigate dose-response efficacy and safety in hemodialysis patients with hyperphosphatemia.

Timeline

Start
2012-01-11
Primary completion
2012-07-03
Completion
2012-07-03

Drugs

EvaluationDrugModalityDoseRoute
Subject PA21 Unknown 750 mg
Subject PA21 Unknown 1500 mg
Subject PA21 Unknown 2250 mg
Subject PA21 Unknown 3000 mg