UnknownPHASE2, PHASE3NCT04219241
Clinical Extension Study for Safety and Efficacy Evaluation of Cellavita-HD Administration in Huntington's Patients.
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, MDAzidus Brasil Scientific Research and Development Ltda
- Intervention
- Cellavita-HD(biological)
- Enrollment
- 35 enrolled
- Eligibility
- 21-65 years · All sexes
- Timeline
- 2020 – 2022
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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