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A 12-Week, Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of Tenapanor for the Treatment of Irritable Bowel Syndrome With Constipation (IBS-C) in Pediatric Patients 12 to Less Than 18 Years Old

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Trial Profile

A 12-Week, Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of Tenapanor for the Treatment of Irritable Bowel Syndrome With Constipation (IBS-C) in Pediatric Patients 12 to Less Than 18 Years Old

Status: Active, no longer recruiting
Phase of Trial: Phase III

Latest Information Update: 09 Jun 2026

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At a glance

  • Drugs Tenapanor (Primary)
  • Indications Constipation; Irritable bowel syndrome
  • Focus Registrational; Therapeutic Use
  • Acronyms R-Ally
  • Sponsors Ardelyx

Most Recent Events

  • 04 Jun 2026 Planned End Date changed from 1 Jun 2026 to 1 Sep 2026.
  • 04 Jun 2026 Planned primary completion date changed from 1 Jun 2026 to 1 Sep 2026.
  • 04 Jun 2026 Status changed from recruiting to active, no longer recruiting.

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