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

L

Leadiant Biosciences

Status

Completed

Conditions

Cerebrotendinous Xanthomatoses

Treatments

Drug: Chenodeoxycholic Acid

Study type

Observational

Funder types

Industry

Identifiers

NCT05499026
CDCA-STUK-15-001

Details and patient eligibility

About

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

Enrollment

28 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

Diagnosis of CTX Received treatment with CDCA Age between 2 and 75 years Having at least one cholestanol level and/or urinary bile alcohol level no more than 3 months prior to treatment with CDCA and one cholestanol level and/or urinary bile alcohol level post-treatment within 2 years from the beginning of therapy with CDCA

Exclusion criteria

Trial contacts and locations

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Data sourced from clinicaltrials.gov

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