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NCT05499026

Safety and Efficacy of CDCA in CTX Chenodeoxycholic Acid (CDCA) in Patients Affected by Cerebrotendinous Xanthomatosis (CTX)

Completed Last updated 12 August 2022
What this trial tests

trial testing Chenodeoxycholic Acid in Cerebrotendinous Xanthomatoses in 28 participants. Completed in 3 June 2015.

Timeline
9 December 2014
Primary endpoint
3 June 2015
3 June 2015

Quick facts

Lead sponsorLeadiant Biosciences Ltd.
StatusCompleted
Study typeOBSERVATIONAL
Enrollment28
Start date9 December 2014
Primary completion3 June 2015
Estimated completion3 June 2015

Drugs / interventions tested

Conditions studied

Sponsor

Leadiant Biosciences Ltd.

Who can join

Eligibility, any sex, with Cerebrotendinous Xanthomatoses. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Retrospective study of CTX patients to investigate the safety and clinical efficacy of Chenodeoxycholic Acid

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Cerebrotendinous Xanthomatoses

Currently open trials in the same condition.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05499026.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing