Hydroxychloroquine Administration for Reduction of Pexophagy

NCT ID: NCT03856866

Last Updated: 2020-12-17

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 3 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-01-11
• Study Completion Date: 2020-05-05

Brief Summary

A series of N-of-1, crossover, randomized, placebo-controlled, double-blinded trial. Hydroxychloroquine (HCQ) and a crossover to placebo (order is randomized and blinded) will be administered in liquid suspension for 84 days (12 weeks) each with an 84 day washout in between. We hypothesize that HCQ will reduce peroxisomal turnover, which will arrest ongoing injury in PBDs caused by PEX1, PEX6 or PEX26.

Detailed Description

HARP is a phase II/III, double-blind, placebo-controlled, randomized, crossover series N-of-1 study of the effect of hydroxychloroquine (HCQ) in patients with peroxisomal biogenesis disorders (PBD-ZSD). Patients eligible for the study must have a laboratory diagnosis of PEX1, PEX6 or PEX26 dependent PBD-ZSD from a CLIA or SCC-certified clinical laboratory, a history of abnormal VLCFA levels, and must be at least 84 days from their last HCQ dose. Patients will be excluded for known sensitivity to HCQ, known glucose-6-phosphate dehydrogenase deficiency, if they have an expected survival of less than 9 months or if they are participating in another interventional clinical trial.

HCQ will be administered at a dose of 4mg/kg/day divided into two doses, as a liquid suspension that can be given orally or through nasogastric or gastric tube. Within the study, HCQ or placebo will be given for 84 days, followed by a washout period of 84 days followed by an 84 day crossover to the alternative therapy to assess the effect the study measures.

Study measures will be completed at four intervals (initiation, end of period 1, start of period 2, end of trial). Ophthalmological monitoring of patients has three components, electroretinogram (ERG), visual acuity testing and optical coherence tomography (OCT). Plasma levels of very long-chain fatty acids (VLCFA), plasmalogen and phytanic acid will be assessed. Parents will also be administered The Pediatric Inventory for Parents (PIP), a questionnaire that was developed to evaluate the stress associated with parenting a seriously ill child, at the end of period 1 and period 2.

Conditions

Zellweger Syndrome; Peroxisome Biogenesis Disorders

Keywords

PBD, Zellweger spectrum, PBD-ZSD

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Hydroxychloroquine

Hydroxychloroquine: liquid suspension, 4mg/kg/day by mouth, divided bid for 84 days.

Group Type: EXPERIMENTAL

Hydroxychloroquine

Intervention Type: DRUG

Hydroxychloroquine: 4mg/kg/day, divided bid.

Placebo

Liquid suspension compounded to mimic the taste, appearance and texture of the investigational agent.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Liquid suspension compounded to mimic the active hydroxycholoquine interventional agent.

Interventions

Hydroxychloroquine

Hydroxychloroquine: 4mg/kg/day, divided bid.

Intervention Type: DRUG

Placebo

Liquid suspension compounded to mimic the active hydroxycholoquine interventional agent.

Intervention Type: DRUG

Other Intervention Names

Apo-Hydroxyquine; Plaquenil

Eligibility Criteria

Inclusion Criteria

• Diagnosed with a peroxisomal defect due to PEX1, PEX6 or PEX26 through a SCC or CLIA-certified clinical genetic testing laboratory.
• Abnormal plasma very-long-chain fatty acid levels.
• All therapies available in Canada have been considered and ruled out, have failed or were justified as being unsuitable for the patient. We note that there are no therapies available.
• At least 84 days from last HCQ dose

Exclusion Criteria

• Known sensitivity to HCQ.
• Known Glucose-6-phosphate dehydrogenase deficiency.
• Expected survival is less than six months.
• The patient does not provide informed consent.
• The patient is participating in another interventional clinical trial.

• Minimum Eligible Age: 6 Months
• Maximum Eligible Age: 40 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

The Hospital for Sick Children

OTHER

Sponsor Role: lead

Responsible Party

Neal Sondheimer

Staff Physician - Clinical and Metabolic Genetics

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Neal Sondheimer, MD

Role: PRINCIPAL_INVESTIGATOR

The Hospital for Sick Children

Locations

The Hospital for Sick Children

Toronto, Ontario, Canada

Countries

Canada

Other Identifiers

1000061385

Identifier Type: -

Identifier Source: org_study_id