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Enrolling by invitationNo phase

Follows people with Parkinson's disease who previously received BRT-DA01 cell therapy

Observes safety and outcomes in people with Parkinson's disease who earlier received BRT-DA01.

Plain-language title generated from the registry record
Registry title: Continued Evaluation of Patients With Parkinson's Disease Who Previously Received BRT-DA01

Key facts

Where
Toronto, CanadaSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 50 and 78 years old?

Source: NCT05897957, who can take part

Where in Canada

  • Toronto Western HospitalToronto, CanadaNo longer taking part

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?
Print a page for my doctor

Trial details

Who runs it
BlueRock Therapeutics
Trial code
NCT05897957
Record updated
12 April 2024
Original description
This is a multicenter study to evaluate the safety and clinical outcomes of BRT-DA01 in subjects with PD who previously received BRT-DA01 in the Phase 1 Study MSK-DA01-101.No investigational therapy will be administered in this study.Read full original descriptionShow less

Continued Evaluation of Patients With Parkinson's Disease Who Previously Received BRT-DA01, a Human Embryonic Stem Cell-Derived Midbrain Dopaminergic Neuronal Cell Therapy

This is a multicenter study to evaluate the safety and clinical outcomes of BRT-DA01 in subjects with PD who previously received BRT-DA01 in the Phase 1 Study MSK-DA01-101.No investigational therapy will be administered in this study.

Inclusion: Subject received BRT-DA01 in Study MSK-DA01-101 (ie, parent study) and will have completed or discontinued the parent study; Subject must be willing and able to provide written informed consent for the BRT-DA0-501 study in accordance with applicable regulations and guidelines and to comply with all study visits and procedures.

Exclusion: No exclusion criteria.

ClinicalTrials.gov NCT05897957