Kikuchi medical clinic
Tsukuba, Ibaraki, Japan
NCT Number: NCT04767581
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.
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Notify Me20 year and older
All sexes
Interventional
Phase 3
Tsukuba, Ibaraki, Japan
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
oral administration
oral administration
Time frame: Week 8
Time frame: Dose period, Week 1, 2, 3, 4, 5, 6, 7, 8.
Time frame: Dose period, Week 1, 2, 3, 4, 5, 6, 7, 8.
Time frame: Dose period, Week 1, 2, 3, 4, 5, 6, 7, 8.
Time frame: Dose period, Week 1, 2, 3, 4, 5, 6, 7, 8.
Time frame: Dose period, Week 1, 2, 3, 4, 5, 6, 7, 8.
Time frame: Dose period, Week 1, 2, 3, 4, 5, 6, 7, 8.
Time frame: Dose period, Week 1, 2, 3, 4, 5, 6, 7, 8.
Kyowa Kirin Co., Ltd.
Industry
A Phase 3, Randomized, Double-blind, Placebo-controlled, Parallel-group Comparative Study of KHK7791 in Hyperphosphatemia Patients on Hemodialysis
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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