CompletedPhase 2NCT03252535
Dose-response Evaluation of the Cellavita HD Product in Patients With Huntington's Disease
Studying Huntington disease
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Azidus Brasil
- Principal Investigator
- Joyce Macedo da Silva, MDAzidus Brasil Scientific Research and Development Ltda
- Intervention
- Cellavita HD lower dose(biological)
- Enrollment
- 49 enrolled
- Eligibility
- 21-65 years · All sexes
- Timeline
- 2018 – 2021
Study locations (1)
- Azidus Brasil Pesquisa Científica e Desenvolvimento Ltda., Valinhos, São Paulo, Brazil
Collaborators
Cellavita Pesquisa Científica Ltda
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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