A Study of INO-A002 in Healthy Dengue Virus-naive Adults

PHASE1CompletedINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

February 7, 2019

Primary Completion Date

October 3, 2022

Study Completion Date

October 3, 2022

Conditions
Healthy Volunteers
Interventions
BIOLOGICAL

INO-A002

Participants will receive one or two 1 ml IM injections (in different arms) into the deltoid region at day 0 (all groups), and in addition on day 3 (in the 2 mg and 4 mg cohorts).

DEVICE

CELLECTRA® 2000

Inoculation will be followed by electroporation with the CELLECTRA® 2000 device.

DEVICE

Dengue Fever Antibodies (IgG)

To determine if the subject is Dengue seronegative at baseline

Trial Locations (1)

19104

University of Pennsylvania, Philadelphia

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Inovio Pharmaceuticals

INDUSTRY

lead

University of Pennsylvania

OTHER

NCT03831503 - A Study of INO-A002 in Healthy Dengue Virus-naive Adults | Biotech Hunter | Biotech Hunter