Phase
Condition
N/ATreatment
Placebo
TS-172 20~60 mg/day
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Hyperphosphatemia patients (outpatients) with chronic kidney disease receivinghemodialysis (HD or HDF) 3 times a week for at least 12 weeks prior to Visit 1 (Week -4)
Patients aged >=18 years at the time of obtaining informed consent
Patients with a serum phosphorus concentration of >= 3.5 mg/dL and < 5.5 mg/dL atVisit 1 (Week -4)
Patients whose serum phosphorus concentration at Visit 3 (Week -2) or Visit 4 (Week -1) has increased by at least 1.0 mg/dL compared with the value at Visit 1 (Week -4)and is >= 5.5 mg/dL and < 10.0 mg/dL.
Exclusion
Exclusion Criteria:
Patients with confirmed serum intact PTH concentration >500 pg/mL from Visit 1 (Week -4) to Visit 5 (Week 0)
Patients with serum phosphorus concentration >= 10.0 mg/dL from Visit 2 (Week -3) toVisit 4 (Week -1)
Patients who have undergone previous parathyroid intervention (PTx, PEIT, etc.)
Study Design
Connect with a study center
Taisho Pharmaceutical Co., Ltd selected site
Tokyo,
JapanSite Not Available
Taisho Pharmaceutical Co., Ltd selected site
Tokyo 1850147,
JapanSite Not Available

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