Dentatorubral-pallidoluysian Atrophy Natural History and Biomarkers Study

Status: Recruiting
Location: See all (3) locations...
Intervention Type: Other
Study Type: Observational
SUMMARY

DRPLA Natural History and Biomarkers Study (DRPLA NHBS) is a prospective observational study that will lay the foundation for clinical trials in DRPLA. The aims of this project are: * To characterize the natural history of DRPLA in both juvenile- and adult-onset patients and study different modalities of biomarkers in this condition. * To identify genetic factors and biomarkers that could predict disease progression. * To provide a platform to support the design and conduct of clinical trials. This study has three arms: 1. Adult Participants: this arm of the study will require participants to be 16 years old or over to participate. 2. Pediatric Participants: this arm of the study will require participants to be under 16 years old to participate. 3. Remote Participants: patients that cannot or do not wish to travel to one of the study sites can participate in this arm of the study, irrespective of their age. Participants will have an annual visit for three years (baseline visit and two follow-up visits, three visits in total). Subjects who complete the whole protocol will be assessed on two consecutive days to reduce patient burden. This project will allow for a better understanding of DRPLA and its course, and therefore allow for future clinical trials on this condition to be more precisely and effectively conducted.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: t
View:

• DRPLA adult participants must be 16 years old or over at the time of enrollment, to participate.

• DRPLA adult participants must have a genetic diagnosis of DRPLA and CAG repeat expansion \>35.

• Patient is able to read, understand, and provide written informed consent (signed and dated). If the patient is under the age of 18 or is unable to provide consent, the patient must have 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.

• Adult pre-symptomatic subjects must have a positive genetic test for the DRPLA expansion without symptoms compatible with the disease, and be 16 years old or over at the time of enrollment.

• Adult Family/Community control participants must be 16 years old or over at the time of enrollment to participate. Blood-relatives must not have a genetic diagnosis of DRPLA or their genetic status is unknown.

⁃ a. DRPLA pediatric participants must be under 16 years old at the time of enrollment, to participate.

⁃ f. DRPLA pediatric participants must have a genetic diagnosis of DRPLA and CAG repeat expansion \>35.

⁃ g. If the patient is under the age of 18 or is unable to provide consent, the patient must have 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.

⁃ h. Pediatric Family/Community control participants must be under 16 years old at the time of enrollment to participate. Blood-relatives must not have a genetic diagnosis of DRPLA or their genetic status is unknown.

Locations
United States
North Carolina
University of North Carolina at Chapel Hill
RECRUITING
Chapel Hill
New York
NYU Grossman School of Medicine
RECRUITING
New York
Other Locations
United Kingdom
University College London
RECRUITING
London
Contact Information
Primary
Paola Giunti
p.giunti@ucl.ac.uk
+44 7899974923
Backup
Hector Garcia-Moreno
h.garcia-moreno@ucl.ac.uk
Time Frame
Start Date: 2022-05-01
Estimated Completion Date: 2026-04
Participants
Target number of participants: 225
Treatments
DRPLA-mutation carrier
Subjects with a positive genetic test for a pathological expansion in the ATN1 gene.
Volunteer control
Subjects without neurological conditions (other than primary headache disorders), without a family history of DRPLA or a previous negative genetic test for pathological expansions in the ATN1 gene.
Sponsors
Collaborators: NYU Langone Health, University of North Carolina, Chapel Hill
Leads: University College, London

This content was sourced from clinicaltrials.gov