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Clinical Trial Summary

This long-term study is designed to evaluate safety and efficacy of KHK7580 orally administered once daily for 52 weeks for patients with secondary hyperparathyroidism receiving hemodialysis.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02549404
Study type Interventional
Source Kyowa Hakko Kirin Co., Ltd
Contact
Status Completed
Phase Phase 3
Start date September 28, 2015
Completion date December 28, 2016

See also
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