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Completed

NCT Number: NCT04767581

Clinical Study of KHK7791 in Hyperphosphatemia Patients on Hemodialysis

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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Key information

Age range

20 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Kikuchi medical clinic

Tsukuba, Ibaraki, Japan

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Has voluntarily provided written informed consent to participate in the study.
  • Aged ≥ 20 years (expressed in completed years) at the time of providing informed consent.
  • Stable chronic renal failure patients who have undergone hemodialysis 3 times per week for at least 12 weeks until screening examination.
  • Dialysis conditions (dialysate, dialyzer, frequency of dialysis per week, dialysis duration, blood flow rate, and dialysate and substitution fluid flow rates), excluding dry weight, should have been unchanged during the last 2 weeks before screening examination.
  • The prescribed drug and dosage regimen should have been unchanged during the last 4 weeks before screening examination.
  • Serum phosphorus levels should be in the range of ≥ 3.5 and ≤ 6.0 mg/dL at screening examination.
  • If on any vitamin D, calcimimetics regimen, bisphosphonate, calcitonin preparations, selective estrogen receptor modulators or teriparatide preparations then the prescribed drug and dosage regimen should have been unchanged for the last 4 weeks before screening examination.
  • Kt/V urea ≥ 1.2 at the most recent test in routine medical practice before screening examination.

Exclusion criteria

  • Peritoneal dialysis was performed within 12 weeks before screening examination.
  • iPTH >600 pg/mL (should be based on the most recent value from the patients' medical records, etc. before pre-enrollment)
  • Having concurrent or a history of inflammatory bowel disease (IBD) or diarrhea-predominant irritable bowel syndrome
  • History of gastrectomy or enterectomy or having undergone gastrointestinal tract surgery within 3 months before screening examination.
  • Subjects who used anti RANKL preparations within 6 weeks before screening examination.
  • Subjects who used anti-sclerostin antibody preparations within 12 weeks before screening examination.
  • Having concurrent severe heart disease or hepatic impairment.
  • Developed cerebrovascular disease or cardiovascular disease requiring hospitalization within 6 months before screening examination.
  • Uncontrollable hypertension or diabetes.
  • Scheduled for living donor kidney transplant, change in the mode of dialysis, home hemodialysis, or change in the dialysis center during the study period.
  • Any diagnosis of and treatment of malignancy within 5 years before screening examination.

Treatment and study plan

KHK7791

Drug

oral administration

Placebo

Drug

oral administration

Primary outcomes

  1. Changes in serum phosphorous levels from baseline values at 8 weeks after the start of administration.

    Time frame: Week 8

Secondary outcomes

  1. Changes in serum phosphorous levels from baseline values at each time point.

    Time frame: Dose period, Week 1, 2, 3, 4, 5, 6, 7, 8.

  2. Achievement/failure of the target serum phosphorus level (serum phosphorus level: ≤ 6.0).

    Time frame: Dose period, Week 1, 2, 3, 4, 5, 6, 7, 8.

  3. Time when the target serum phosphorus level (serum phosphorus level: ≤ 6.0) was achieved.

    Time frame: Dose period, Week 1, 2, 3, 4, 5, 6, 7, 8.

  4. Achievement/failure of the target serum phosphorus level (serum phosphorus level: ≤ 5.5).

    Time frame: Dose period, Week 1, 2, 3, 4, 5, 6, 7, 8.

  5. Time when the target serum phosphorus level (serum phosphorus level: ≤ 5.5) was achieved.

    Time frame: Dose period, Week 1, 2, 3, 4, 5, 6, 7, 8.

  6. Concentrations of such as Ca × P product levels at each time point.

    Time frame: Dose period, Week 1, 2, 3, 4, 5, 6, 7, 8.

  7. Changes of such as Ca × P product levels from baseline values at each time point.

    Time frame: Dose period, Week 1, 2, 3, 4, 5, 6, 7, 8.

Sponsors and collaborators

Lead sponsor

Kyowa Kirin Co., Ltd.

Industry

Registry information

Official study title

A Phase 3, Randomized, Double-blind, Placebo-controlled, Parallel-group Comparative Study of KHK7791 in Hyperphosphatemia Patients on Hemodialysis

Important dates

Study start
2021
Primary completion
2021
Study completion
2021
First posted
Feb 23, 2021
Registry last updated
Sep 8, 2021

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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