drugset / Trial / NCT02549417

Phase 3 Study of KHK7580

NCT02549417

Phase 3 Completed 39 enrolled Kyowa Kirin, Inc.
NaSingle-groupOpen-labelTreatment

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.

Timeline

Start
2015-09-29
Primary completion
2016-12-22
Completion
2016-12-22

Drugs

EvaluationDrugModalityDoseRoute
Subject EVOCALCET Small molecule Oral