UnknownPhase 1NCT02728115

Safety Evaluation of Cellavita HD Administered Intravenously in Participants With Huntington's Disease

Studying Huntington disease

Last synced from ClinicalTrials.gov

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Key facts

Sponsor
Azidus Brasil
Principal Investigator
Joyce Macedo da Silva, MD
Azidus Brasil Scientific Research and Development Ltda
Intervention
Cellavita HD Lower Dose(biological)
Enrollment
6 enrolled
Eligibility
21-65 years · MALE
Timeline
20172023

Study locations (1)

Collaborators

Cellavita Pesquisa Científica Ltda · Azidus Brasil Scientific Research and Development 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.

Open NCT02728115 on ClinicalTrials.gov

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