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Completed

NCT Number: NCT03831607

A Phosphate Binder Switch Study of KHK7791 in Hyperphosphatemia Patients on HD

To evaluate the effect and safety of a switch from phosphate binders to KHK7791 to treat Hyperphosphatemia in patients on HD.

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Key information

Age range

20 year–79 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Study Site 1

Niigata, Japan

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Stable chronic renal failure patients who have undergone hemodialysis 3 times per week for at least 12 weeks until screening examination.
  • Met certain conditions for dialysis excluding Dry Weight (Dialysate, Dialyzer, Frequency of Dialysis per Week, Dialysis Time, Blood Flow Rate, and Dialysate and Substitution Fluid Flow Rate) 2 weeks before screening examination.
  • Taking at least 2 tablets of phosphate binder 3 times per day. The prescribed dosage regimen should have been unchanged for the period from 2 weeks before screening examination through pre-enrollment.
  • Serum phosphorus levels should be between 3.5 and 7.0 mg/dL (inclusive) at screening examination.
  • If on any vitamin D or calcimimetics regimen, the dosage regimen should have been unchanged for the last 2 weeks before screening examination.

Exclusion criteria

  • iPTH > 600 pg/mL (should be based on the most recent value from patient's medical records before pre-enrollment)
  • History of inflammatory bowel disease (IBD) or diarrhea predominant irritable bowel syndrome
  • History of gastrectomy or enterectomy (excluding endoscopic resection and cecectomy) or having undergone gastrointestinal tract surgery within 3 months before screening examination.
  • Severe heart disease (including congestive heart failure, defined as New York Heart Association [NYHA] cardiac functional classification of Class III or IV, and vascular lesions requiring hospitalization such as myocardial infarction), hepatic impairment (including AST/ALT ≥ 100 U/L before the start of observation period), or concurrent cirrhosis.
  • Developed cerebrovascular disease (such as cerebral infarction and cerebral hemorrhage) or cardiovascular disease (such as acute myocardial infarction and unstable angina) 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 plans to change the dialysis center (relocate to another hospital/clinic) during the study period.
  • Any diagnosis of or treatment of malignancy within 5 years before screening examination (excluding basal cell carcinoma or surgically resected intraepithelial carcinoma of uterine cervix).

Treatment and study plan

KHK7791

Drug

KHK7791 30 mg, 20 mg ,10 mg or 5 mg tablets

Other names: Tenapanor

Primary outcomes

  1. Percentage of subjects who reduce the total number of taking phosphate binder tablets at the last assessment from baseline.

    Time frame: Week 26

Secondary outcomes

  1. Serum phosphorus levels at each time point after the start of treatment

    Time frame: up to Week 26

  2. Corrected serum calcium level at each time point after the start of treatment

    Time frame: up to Week 26

Sponsors and collaborators

Lead sponsor

Kyowa Kirin Co., Ltd.

Industry

Registry information

Official study title

A Phase 2, Open-label Phosphate Binder Switch Study of KHK7791 in Hyperphosphatemia Patients on Hemodialysis

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Feb 6, 2019
Registry last updated
Mar 7, 2024

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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