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Enrolling by invitation Observational

AB-1005 Long-Term Follow-up Study

NCT07081841 · tracked via the Priya Life Science USA tracker
Sponsor
Phase
Observational
Started
2025-09-04
Last updated
2025-10-02

Condition(s) studied

Parkinson's DiseaseMultiple System Atrophy, Parkinson Variant

Investigational drug(s) / intervention(s)

Observation

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.

Study summary

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.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
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

Primary outcome measure(s)

  • Long term safety and tolerability — Up to 10 years post surgery
    Measure of the occurrence of serious and non-serious adverse events

Trial sites (2)

FacilityCityRegionStatus
University of California San Francisco San Francisco California
Ohio State University Columbus Ohio
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07081841 on ClinicalTrials.gov ↗ ← All trials in the USA