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: Completed

Phase of Trial: Phase III

Latest Information Update: 09 Jun 2026

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At a glance

04 Jun 2026 Actual Primary Completion date changed to 6 May 2026.
04 Jun 2026 Status changed from active, no longer recruiting to completed.
02 Jun 2026 Primary endpoint (Percentage of Participants Response defined as Alkaline phosphatase (ALP) 1.0 Upper Limit of Normal (ULN) AND 15% Decrease in ALP at Week 52.) has been met, according to a Gilead Sciences Media Release.

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