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A Phase II Study to Evaluate Safety, Tolerability and Efficacy, of CS0159 in Patients Subjects With Primary Sclerosing Cholangitis, Multicenter, Randomized, 12-week Double-blind, Placebo-controlled, and 40-week Open Study

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Trial Profile

A Phase II Study to Evaluate Safety, Tolerability and Efficacy, of CS0159 in Patients Subjects With Primary Sclerosing Cholangitis, Multicenter, Randomized, 12-week Double-blind, Placebo-controlled, and 40-week Open Study

Status: Recruiting
Phase of Trial: Phase II

Latest Information Update: 20 Mar 2025

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At a glance

  • Drugs Linafexor (Primary)
  • Indications Primary sclerosing cholangitis
  • Focus Adverse reactions; Therapeutic Use
  • Sponsors Cascade Pharmaceuticals

Most Recent Events

  • 14 Mar 2025 Planned End Date changed from 1 Dec 2024 to 1 Nov 2025.
  • 14 Mar 2025 Planned primary completion date changed from 1 Dec 2024 to 1 Oct 2025.
  • 31 Aug 2023 Status changed from not yet recruiting to recruiting.

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