CompletedPhase 1NCT04093076

Dose-ranging Study: Safety, Tolerability and Immunogenicity of INO-4500 in Healthy Volunteers in Ghana

Studying Lassa fever

Last synced from ClinicalTrials.gov

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Key facts

Sponsor
Inovio Pharmaceuticals
Principal Investigator
Bonaventure Orizu, MD
Inovio Pharmaceuticals
Intervention
INO-4500(drug)
Enrollment
220 enrolled
Eligibility
18-50 years · All sexes
Timeline
20212022

Study locations (1)

Collaborators

Coalition for Epidemic Preparedness Innovations

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 NCT04093076 on ClinicalTrials.gov

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