NCT01668186View on ClinicalTrials.gov

Longitudinal Natural History Study of Patients With Peroxisome Biogenesis Disorders (PBD)

RecruitingOBSERVATIONAL
Enrollment

244

Participants

Timeline

Start Date

January 31, 2012

Primary Completion Date

January 31, 2025

Study Completion Date

January 31, 2025

Conditions
Peroxisome Biogenesis DisorderZellweger Spectrum DisorderRCDP - Rhizomelic Chondrodysplasia PunctataD-Bifunctional Protein DeficiencyAlpha-Methylacyl-CoA Racemase DeficiencyPeroxisomal Acyl-CoA Oxidase DeficiencyPeroxisomal Acyl-CoA Oxidase 2 DeficiencyATP Binding Cassette Subfamily D Member 3 Gene MutationACBD5 (AcylCoA Binding Domain 5) DeficiencyAdult Refsum DiseaseSterol Carrier Protein 2 Deficiency
Trial Locations (1)

H4A 3J1

RECRUITING

Research Institute of the McGill University Health Center, Montreal

All Listed Sponsors
lead

McGill University Health Centre/Research Institute of the McGill University Health Centre

OTHER