A Phase 3 Study of Tenapanor to Treat Hyperphosphatemia in ESRD Patients on Dialysis
Trial details
- Registry ID
- NCT03427125
- Phase
- Phase 3
Company identity has not yet been verified
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Research sample: selected versions from May 2023 onward plus a preceding baseline where available. Only selected fields were retained; endpoint measures were truncated to 300 characters. This is not complete trial or sponsor history. Daily snapshots begin when collection starts.
| Trial | Sponsor | Phase | Status | Primary completion |
|---|---|---|---|---|
| A Phase 3 Study of Tenapanor to Treat Hyperphosphatemia in ESRD Patients on DialysisNCT03427125 | Ardelyx | Phase 3 | Completed | 2019-11-15Actual |
| Study to Assess Safety and Efficacy of Tenapanor for Treatment of IBS-C in Pediatric Patients 12 to Less Than 18 YearsNCT05643534 | Ardelyx | Phase 3 | Completed | 2026-08-20Actual |
| Safety Study of Tenapanor for the Treatment of Pediatric Patients (6 to Less Than 18 Years Old) With IBS-CNCT05905926 | Ardelyx | Phase 3 | Enrolling by invitation | 2031-07Estimated |
| 4-Week, Multi-center Dose-Ranging Study for the IBS-C in Pts. 6 to <12 YrsNCT06553547 | Ardelyx | Phase 2 | Completed | 2026-07-07Actual |
| A 26-Wk Study to Assess Safety & Efficacy of Tenapanor for T/t of Chronic Idiopathic Constipation in AdultsNCT07382167 | Ardelyx | Phase 3 | Recruiting | 2027-02-26Estimated |
NCT05643534 · Ardelyx
Estimated
Actual
2026-09-01
2026-08-20
Active not recruiting
Completed
NCT06553547 · Ardelyx
Estimated
Actual
2026-07
2026-07-07
Active not recruiting
Completed
NCT06553547 · Ardelyx
Estimated
Actual
2026-06
2026-07
Recruiting
Active not recruiting
NCT05643534 · Ardelyx
Estimated
Actual
2026-06-01
2026-09-01
Recruiting
Active not recruiting
NCT07382167 · Ardelyx
measure: Durable CSBM response
measure: Durable complete spontaneous bowel movements (CSBM) response
The saved outcome text may be shortened. Check the source for full wording.
NCT05643534 · Ardelyx
2025-12-31
2026-06-01