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.
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