drugset / Trial / NCT02549417
Phase 3 Study of KHK7580
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | EVOCALCET | Small molecule | — | Oral |