drugset / Trial / NCT03226171

Dose Adjustment Trial of SK-1403 in Hemodialysis Patients With Secondary Hyperparathyroidism

NCT03226171 ↗

Phase 2 Completed 58 enrolled Sanwa Kagaku Kenkyusho Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

This study is conducted to assess the efficacy and safety of SK-1403 in Hemodialysis Patients with Secondary Hyperparathyroidism. In the first treatment period, the efficacy of SK-1403 is assessed after 18 weeks of treatment with SK-1403 individually dose-adjusted . Safety is also assessed during this period. Patients who completed the first treatment period proceed to the second treatment period and receive the treatment with SK-1403 for 34 weeks. Efficacy and safety of SK-1403 are also assessed during this period.

Timeline

Start
2017-06-20
Primary completion
2018-09-11
Completion
2018-09-11

Drugs

EvaluationDrugModalityDoseRoute
Subject UPACICALCET Small molecule — —