Success Metrics

Clinical Success Rate
100.0%

Based on 11 completed trials

Completion Rate
100%(11/11)
Active Trials
3(20%)
Results Posted
73%(8 trials)

Phase Distribution

Ph phase_3
7
47%
Ph phase_1
1
7%
Ph phase_4
4
27%
Ph phase_2
3
20%

Phase Distribution

1

Early Stage

3

Mid Stage

11

Late Stage

Phase Distribution15 total trials
Phase 1Safety & dosage
1(6.7%)
Phase 2Efficacy & side effects
3(20.0%)
Phase 3Large-scale testing
7(46.7%)
Phase 4Post-market surveillance
4(26.7%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

100.0%

11 of 11 finished

Non-Completion Rate

0.0%

0 ended early

Currently Active

3

trials recruiting

Total Trials

15

all time

Status Distribution
Active(4)
Completed(11)

Detailed Status

Completed11
Recruiting3
Enrolling by invitation1

Development Timeline

Analytics

Development Status

Total Trials
15
Active
3
Success Rate
100.0%
Most Advanced
Phase 4

Trials by Phase

Phase 11 (6.7%)
Phase 23 (20.0%)
Phase 37 (46.7%)
Phase 44 (26.7%)

Trials by Status

recruiting320%
enrolling_by_invitation17%
completed1173%

Recent Activity

Clinical Trials (15)

Showing 15 of 15 trials
NCT06810167Phase 3

Assessing Tenapanor as a Treatment of CF-related Constipation.

Recruiting
NCT05995899Phase 4

Effect of Tenapanor on the Metagenomics and Metabolomics of Patients With Irritable Bowel Syndrome With Constipation

Completed
NCT06481150Phase 4

A Novel Approach for Reducing Hyperoxaluria and Kidney Stone Risk.

Completed
NCT06553547Phase 2

4-Week, Multi-center Dose-Ranging Study for the IBS-C in Pts. 6 to <12 Yrs

Recruiting
NCT05905926Phase 3

Safety Study of Tenapanor for the Treatment of Pediatric Patients (6 to Less Than 18 Years Old) With IBS-C

Enrolling By Invitation
NCT06460038Phase 2

Tenapanor in Synucleinopathy-Related Constipation

Recruiting
NCT06203444Phase 1

An Open-label Study to Evaluate the Pharmacokinetics of Oral Tenapanor in Breast Milk of Lactating Females

Completed
NCT03427125Phase 3

A Phase 3 Study of Tenapanor to Treat Hyperphosphatemia in ESRD Patients on Dialysis

Completed
NCT04549597Phase 4

Study to Evaluate the Use of Tenapanor as Core Therapy in the Treatment of Hyperphosphatemia

Completed
NCT03988920Phase 4

A Long-Term Study of Tenapanor Alone or in Combination With Sevelamer in Patients With CKD on Dialysis and HP

Completed
NCT03824587Phase 2

Study to Evaluate the Efficacy of Tenapanor as Adjunctive Therapy to Phosphate Binder Therapy

Completed
NCT02727751Phase 3

A Long-Term Safety Study of Tenapanor for the Treatment of IBS-C

Completed
NCT02675998Phase 3

An 8-Week Study to Evaluate Tenapanor in the Treatment of Hyperphosphatemia in End-Stage Renal Disease Patients on Hemodialysis (ESRD-HD)

Completed
NCT02686138Phase 3

A 26-Week Study to Evaluate the Efficacy and Safety of Tenapanor in IBS-C

Completed
NCT02621892Phase 3

A 12-Week Study With a 4-Week Randomized Withdrawal Period to Evaluate the Efficacy and Safety of Tenapanor for the Treatment of IBS-C

Completed

All 15 trials loaded

Drug Details

Intervention Type
DRUG
Total Trials
15