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A Long-term Study of TS-172 in Hyperphosphatemia Patients on Hemodialysis

RecruitingPhase 3Ages 18 Years - anyAllTaisho Pharmaceutical Co., Ltd.
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In plain words

What the trial is, and whether it could suit you

A clinical study to evaluate the long-term safety and efficacy of TS-172 in hyperphosphatemia patients on hemodialysis.

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๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria: 1. Hyperphosphatemia patients (outpatients) with chronic kidney disease receiving hemodialysis (HD or HDF) 3 times a week for at least 12 weeks prior to Visit 1 (Week -2) 2. Patients aged โ‰ฅ18 years at the time of obtaining informed consent 3. Patients who have been prescribed at least one phosphate binder within the approved dosage, and the prescribed drug and dosage regimen should have been unchanged during the last 2 weeks prior to Visit 1 (Week -2) 4. Patients with a serum phosphorus concentration of โ‰ฅ 3.5 mg/dL and โ‰ค 7.0 mg/dL at Visit 1 (Week -2) or Visit 2 (Week -1) Exclusion Criteria: 1. Patients with confirmed serum intact PTH concentration \>500 pg/mL at Visit 1 (Week -2) 2. Patients who have undergone previous parathyroid intervention (PTx, PEIT, etc.)
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What it tests

  • TS-172
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Where

1 site
Taisho Pharmaceutical Co., Ltd selected site
Tokyo, Japan
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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