Trial Profile

IDEAL: A 52-week, Double-blind, Placebo-controlled, Randomized, Phase 3 Study Intended to Determine the Effects of Seladelpar on Normalization of Alkaline Phosphatase Levels in Subjects With Primary Biliary Cholangitis (PBC) and an Incomplete Response or Intolerance to Ursodeoxycholic Acid (UDCA)

Status: Recruiting

Phase of Trial: Phase III

Latest Information Update: 16 Apr 2025

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At a glance

24 Mar 2025 Planned number of patients changed from 150 to 90.
24 Mar 2025 Planned End Date changed from 1 Dec 2025 to 1 Jun 2026.
24 Mar 2025 Planned primary completion date changed from 1 Dec 2025 to 1 Jun 2026.

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