CClinicalTrials.gg
CompletedNCT02549404Updated Jul 5, 2017

Phase 3 Study of KHK7580

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

Phase
Phase 3
Study type
Interventional
Enrollment
137
Allocation
Not applicable
Ages
20 Years and older
Sex
All
01

Study summary

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.

02

Conditions studied

03

In context

Neoplasm Metastasis

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 →

Lead sponsor

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.

04

Who can participate

Ages eligible
20 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

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 PTH level of > 240 pg/ml at screening (except subjects receiving cinacalcet hydrochloride at screening)

Exclusion criteria

Exclusion Criteria:

  • Change in dose or dosing regimen of cinacalcet hydrochloride or activated vitamin D drug or its derivative, phosphate binder, or calcium preparation within 2 weeks before screening; or start of treatment with such drugs within 2 weeks before screening;
  • Parathyroidectomy and/or parathyroid intervention within 24 weeks before screening;
  • Severe heart disease;
  • Severe hepatic dysfunction;
  • Uncontrolled hypertension and/or diabetes;
  • Treatment with an investigational product (drug or medical device) in a clinical study or any study equivalent to clinical study within 12 weeks before screening;
  • Primary hyperparathyroidism;
  • Other conditions unfit for participation in this study at the discretion of the investigator or subinvestigator.
05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
137 participants (actual)

Study arms

  • Experimental
    KHK7580

    Drug: KHK7580

Interventions

  • DrugKHK7580

    Oral administration

06

What researchers measure

Primary outcomes

  1. Number of participants with adverse events

    Adverse Event collection and assessment

    Time frame: Up to 52 weeks

Secondary outcomes

  1. Percentage of subjects achieving intact parathyroid hormone (PTH) level of ≥ 60 pg/mL and ≤ 240 pg/mL

    Time frame: Up to 52 weeks

  2. 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

  3. Mean percent change in intact PTH level from baseline

    Time frame: Up to 52 weeks

07

Study locations

1 site
  • For additional information regarding investigative sites for this trial, contact Kyowa Hakko Kirin
    Tokyo, Japan
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 5, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02549404
Lead sponsor
Kyowa Kirin Co., Ltd.
Responsible party
Sponsor
First posted
Sep 15, 2015
Start date
Sep 28, 2015
Primary completion
Dec 6, 2016
Completion
Dec 28, 2016
Last update
Jul 5, 2017

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2017. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion