Evaluate the Safety, Tolerability and Immunogenicity Study of GLS-5300 in Healthy Volunteers

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

60

Participants

Timeline

Start Date

August 28, 2018

Primary Completion Date

May 30, 2019

Study Completion Date

April 22, 2020

Conditions
Healthy
Interventions
BIOLOGICAL

GLS-5300

\[Part A\] GLS-5300 0.3 mg at 0, 4, and 12 weeks (N=5) \[Part B\] GLS-5300 0.3 mg at 0, 4, and 12 weeks (N=5) GLS-5300 0.6 mg at 0, 4, and 12 weeks (N=25) GLS-5300 0.6 mg at 0 and 8 weeks (N=25)

DEVICE

Cellectra 2000 Electroporation

GLS-5300 administered ID followed by Cellectra 2000 Electroporation

Trial Locations (2)

Unknown

Seoul National University Bundang Hospital, Seongnam

Seoul National University Hospital, Seoul

Sponsors
All Listed Sponsors
collaborator

Inovio Pharmaceuticals

INDUSTRY

collaborator

International Vaccine Institute

OTHER

lead

GeneOne Life Science, Inc.

INDUSTRY

NCT03721718 - Evaluate the Safety, Tolerability and Immunogenicity Study of GLS-5300 in Healthy Volunteers | Biotech Hunter | Biotech Hunter