drugset / Trial / NCT04767581

Clinical Study of KHK7791 in Hyperphosphatemia Patients on Hemodialysis

NCT04767581

Phase 3 Completed 165 enrolled Kyowa Kirin, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

To evaluate the efficacy of KHK7791 by comparing changes in serum phosphorus levels from baseline values between hemodialysis patients with hyperphosphatemia receiving repeated administration of KHK7791 for 8 weeks and those receiving placebo.

Timeline

Start
2021-03-08
Primary completion
2021-08-10
Completion
2021-08-10

Drugs

EvaluationDrugModalityDoseRoute
Comparator Tenapanor Small molecule 5 mg Oral
Comparator Tenapanor Small molecule 10 mg Oral
Comparator Tenapanor Small molecule 20 mg Oral
Comparator Tenapanor Small molecule 30 mg Oral

Indications