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Enrolling by invitationPhase 4

Long-term follow-up of people with Parkinson's disease or MSA who received AB-1005

Follows people with Parkinson's disease or MSA who earlier received AB-1005 gene transfer.

Plain-language title generated from the registry record
Registry title: AB-1005 Long-Term Follow-up Study

Key facts

Where
Gdansk and Katowice, PolandSee the 2 sites
Phase
Phase 4

Where in Poland

  • Copernicus Podmiot Leczniczy Sp. z o.oGdansk, PolandNot yet recruiting
  • Specjalistyczna Praktyka Lekarska, Prof. Grzegorz OpalaKatowice, PolandNot yet recruiting

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
AskBio Inc
Trial code
NCT07081841EU 2025-522653-19-00
Record updated
2 October 2025
Original description
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.Read full original descriptionShow less

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

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.

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

Exclusion: There are no exclusion criteria.

ClinicalTrials.gov NCT07081841 · EU CTIS 2025-522653-19-00