A Clinical Study of TS-172 in Hyperphosphatemia Patients on Hemodialysis

Recruiting Phase 3 Interventional Study
Hyperphosphatemia Patients on Hemodialysis
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Pivotal Trial This treatment is in the last trial phase before FDA approval. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 3
Study type
Interventional
Purpose
Treatment
Participants needed
30 (estimated)
Sponsor
Taisho Pharmaceutical Co., Ltd. · Industry
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About This Trial

An open-label, single-arm clinical study of TS-172 in hyperphosphatemia patients on hemodialysis

Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Hyperphosphatemia patients (outpatients) with chronic kidney disease receiving hemodialysis (HD or HDF) 3 times a week at least 12 weeks prior to Visit 1 (Week -4) 2. Patients aged \>= 18 years at the time of obtaining informed consent 3. Patients who are receiving at least o…
Contacts

Taisho Pharmaceutical Co., Ltd.

81-3-3985-1118

shu_chiken@taisho.co.jp

CONTACT