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To investigate dose-response efficacy and safety in hemodialysis patients with hyperphosphatemia.
Age
20 - No limit years
Sex
ALL
Healthy Volunteers
No
Japan
Multiple Locations, Japan
Start Date
January 11, 2012
Primary Completion Date
July 3, 2012
Completion Date
July 3, 2012
Last Updated
August 23, 2018
183
ACTUAL participants
PA21
DRUG
PA21
DRUG
PA21
DRUG
PA21
DRUG
Placebo
DRUG
Lead Sponsor
Kissei Pharmaceutical Co., Ltd.
NCT06960304
NCT06771973
Data Source & Attribution
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