drugset / Trial / NCT06810167

Assessing Tenapanor as a Treatment of CF-related Constipation.

NCT06810167

Phase 3 Recruiting 25 enrolled Massachusetts General Hospital Ardelyx · collab
NaSingle-groupOpen-labelTreatment

Summary

Tenapanor is the newest FDA-approved drug for IBS with constipation (IBS-C). This study seeks to understand tenapanor as a treatment for cystic fibrosis-related constipation (CFrC) in CF patients. Participants will ingest one 50 mg tablet of tenapanor, twice daily, for a 4-week treatment period. They will also complete three questionnaires, the PAC-SYM, PAC-QoL, and IBS-SSS, and daily diaries to characterize GI symptom burden and spontaneous bowel movement (SBM) frequency.

Timeline

Start
2025-06-01
Primary completion
2026-06-30
Completion
2027-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Tenapanor Small molecule 50 mg Oral