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Clinical Trial Summary

This study is designed to evaluate efficacy and safety of KHK7580 orally administered once daily for 32 weeks for patients with secondary hyperparathyroidism receiving peritoneal dialysis. After 32-week treatment period, the subjects will receive KHK7580 in the 20-week extension period to evaluate long-term safety and efficacy.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02549417
Study type Interventional
Source Kyowa Hakko Kirin Co., Ltd
Contact
Status Completed
Phase Phase 3
Start date September 29, 2015
Completion date December 22, 2016

See also
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