Clinical Trial: A Phase III Study of PA21 in Peritoneal Dialysis Patients With Hyperphosphatemia
Study Status: Completed
Recruit Status: Completed
Study Type: Interventional
Official Title:
Brief Summary: The purpose of this study is to investigate efficacy and safety, when administering PA21, in peritoneal dialysis patients having hyperphosphatemia.
Detailed Summary:
Sponsor: Kissei Pharmaceutical Co., Ltd.
Current Primary Outcome: Serum phosphate concentrations [ Time Frame: 12 weeks ]
Original Primary Outcome: Same as current
Current Secondary Outcome:
- Incidences of Adverse Events [ Time Frame: 12 weeks ]
- Incidences of Adverse Events [ Time Frame: 28 weeks ]
- Serum phosphate concentrations [ Time Frame: 28 weeks ]
Original Secondary Outcome: Same as current
Information By: Kissei Pharmaceutical Co., Ltd.
Dates:
Date Received: May 7, 2013
Date Started:
Date Completion:
Last Updated: November 11, 2014
Last Verified: November 2014