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TerminatedNCT03359174

An Efficacy Trial of Low Dose All-trans Retinoic Acid in Patients With Primary Sclerosing Cholangitis

An Efficacy Trial of Low Dose All-trans Retinoic Acid (ATRA) in Patients With Primary Sclerosing Cholangitis

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
2 (actual)
Sponsor
Yale University · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The purpose of this research study is to determine whether a low dose of ATRA will improve laboratory tests of liver and bile duct inflammation in patients with PSC. The investigators will also look for changes to other blood tests which are related to inflammation, scarring, and the immune system.

Conditions

Interventions

TypeNameDescription
DRUGAll-trans retinoic acidFixed low dose of ATRA 10 mg twice daily for 24 weeks.

Timeline

Start date
2018-05-29
Primary completion
2020-12-01
Completion
2021-01-01
First posted
2017-12-02
Last updated
2021-08-09
Results posted
2021-08-09

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT03359174. Inclusion in this directory is not an endorsement.

An Efficacy Trial of Low Dose All-trans Retinoic Acid in Patients With Primary Sclerosing Cholangitis (NCT03359174) · Clinical Trials Directory