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Enrolling by invitation NCT07081841

AB-1005 Long-Term Follow-up Study

Observational Parkinson's Disease Multiple System Atrophy, Parkinson Variant

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Observation.
Who it may be relevant to
Registry conditions: Parkinson's Disease, Multiple System Atrophy, Parkinson Variant. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Long-Term Safety and Efficacy Follow-up of AB-1005 Gene Transfer Study Participants With Parkinson's Disease or Multiple System Atrophy

Overview

This is an observational, long term, follow-up study for participants with Parkinson's disease (PD) or Multiple System Atrophy-Parkinsonian subtype (MSA-P) who participated in prior interventional studies with AB-1005. It is intended to better understand the long-term safety of AB-1005, how well tolerated it is and how long lasting the effects are.

Interventions

  • Other Observation
    This is an observational study in which safety laboratories and non-invasive routine clinical assessments are conducted to gauge long term safety and efficacy.

Primary outcome measures

  • Long term safety and tolerability [Time frame: Up to 10 years post surgery]

Eligibility criteria

Inclusion criteria

  • PD and MSA-P participants that are or were enrolled in an interventional AB-1005 study and provide informed consent

Exclusion criteria

  • There are no exclusion criteria

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

United States · 2 centers
  • University of California San Francisco — San Francisco
  • Ohio State University — Columbus

Identifiers

NCT: NCT07081841 · ASK-PD0-CS002

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗