Phase 3 long-term study of KHK7580

Phase 3 study of KHK7580 (A Long-term Study of KHK7580 in Subjects with Secondary Hyperparathyroidism Receiving Hemodialysis)

Status

Unknown

Phases

Phase 3

Study type

Interventional

Source

JPRN

Registry ID

JPRN-jRCT2080222963

Enrollment

120

Registered

2015-09-10

Start date

2015-09-10

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Secondary hyperparathyroidism receiving hemodialysis

Interventions

investigational material(s) Generic name etc : KHK7580 INN of investigational material : Therapeutic category code : 399 Agents affecting metabolism, n.e.c. Dosage and Administration for Investigatio

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: - Personally submitted written voluntary informed consent to participate in the study - Stable chronic renal disease treated with hemodialysis 3 times weekly for at least 12 weeks before screening - Intact parathyroid hormone (PTH) level of > 240 pg/ml at screening (except subjects receiving cinacalcet hydrochroride at screening)

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Safety Adverse Event	—

Secondary

Measure	Time frame
Efficacy Number and percentage of subjects achieving intact PTH level of >= 60 pg/mL and =< 240 pg/mL	—

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026