A Phase 3 interventional study of KHK7580 in Secondary Hyperparathyroidism, sponsored by Kyowa Kirin Co., Ltd.. Completed at 1 site in Japan. Open to participants aged 20 Years and older. Per ClinicalTrials.gov, last updated 2017-07-05.
Sponsored by Kyowa Kirin Co., Ltd. · Phase 3, Interventional, and Treatment
This long-term study is designed to evaluate safety and efficacy of KHK7580 orally administered once daily for 52 weeks for patients with secondary hyperparathyroidism receiving hemodialysis.
3,517 studies on the registry are indexed under Neoplasm Metastasis; 885 are open to participants now.
This study's enrollment of 137 is above the median of 54 across 2,767 interventional studies indexed under Neoplasm Metastasis.
Browse Neoplasm Metastasis studies →Kyowa Kirin Co., Ltd. is the lead sponsor of 155 studies on the registry; 10 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
Drug: KHK7580
Oral administration
Number of participants with adverse events
Adverse Event collection and assessment
Time frame: Up to 52 weeks
Percentage of subjects achieving intact parathyroid hormone (PTH) level of ≥ 60 pg/mL and ≤ 240 pg/mL
Time frame: Up to 52 weeks
Percentage of subjects achieving a mean percent decrease in intact PTH level of ≥ 30% (percent change ≤ -30%) from baseline
Time frame: Up to 52 weeks
Mean percent change in intact PTH level from baseline
Time frame: Up to 52 weeks
This study is completed, as verified in Jul 2017. You cannot join it, but the record below documents what was studied.
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Kyowa Kirin Co., Ltd.