A Long-term Study of PA21 in Hemodialysis Patients With Hyperphosphatemia
NCT01833494 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 161
Last updated 2018-10-09
Summary
The purpose of this study is to investigate the safety and efficacy for 52-week dosing in hemodialysis patients with hyperphosphatemia.
Conditions
- Hemodialysis Patients With Hyperphosphatemia
Interventions
- DRUG
-
PA21
Sponsors & Collaborators
-
Kissei Pharmaceutical Co., Ltd.
lead INDUSTRY
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 20 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2013-03-18
- Primary Completion
- 2014-08-31
- Completion
- 2014-08-04
Countries
- Japan
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