Integrated Prospective and Retrospective Observational Study to Characterize Biomarkers and Disease Progression in Patients With Pelizaeus-Merzbacher Disease

Status: Recruiting
Location: See all (4) locations...
Study Type: Observational
SUMMARY

The purpose of the study is to prospectively assess longitudinal changes in proteolipid protein 1 (PLP1) protein, disease-related biomarkers in cerebral spinal fluid (CSF) and blood, neuroimaging parameters relevant to Pelizaeus-Merzbacher disease (PMD) and longitudinal changes in performance on clinical, participant, and caregiver-reported outcome assessments to inform the development of therapies for PMD.

Eligibility
Participation Requirements
Sex: Male
Minimum Age: 6 months
Maximum Age: 17
Healthy Volunteers: f
View:

• Participant has a parent or caregiver capable of providing informed consent (signed and dated) and able to attend all scheduled study visits and provide feedback regarding the participant's symptoms and performance as described in the protocol and be able to comply with all study requirements

• Participant has a diagnosis of Pelizaeus-Merzbacher Disease with genetic confirmation of PLP1 duplication

• Male, 6 months-17 years old, inclusive, at the time of informed consent and phenotype consistent with classic PMD

• No contraindications for lumbar punctures (LPs), blood draws, neuroimaging, sedation (if necessary) or other study procedures

Locations
Other Locations
France
Ionis Investigative Site
RECRUITING
Clermont-ferrand
Ionis Investigative Site
RECRUITING
Le Kremlin-bicêtre
Germany
Ionis Investigative Site
RECRUITING
Göttingen
Netherlands
Ionis Investigative Site
RECRUITING
Amsterdam
Contact Information
Primary
Ionis Pharmaceuticals
IonisPelizaeusMerzbacherStudy@clinicaltrialmedia.com
(844) 430-1848
Time Frame
Start Date: 2022-10-03
Estimated Completion Date: 2029-03
Participants
Target number of participants: 32
Treatments
Pelizaeus-Merzbacher Disease Participants
Participants will undergo CSF collection and neuroimaging procedures, up to Week 106 as a part of prospective study. Each participant's medical and family history data will be collected retrospectively from available medical notes and charts, from birth up to the end of the study period (up to 26 months).
Sponsors
Leads: Ionis Pharmaceuticals, Inc.

This content was sourced from clinicaltrials.gov