A Clinical Trial to Evaluate the Safety and Immunogenicity of rVSV∆G-LASV-GPC Vaccine in Adults in Good General Heath

PHASE1Active, not recruitingINTERVENTIONAL
Enrollment

114

Participants

Timeline

Start Date

June 23, 2021

Primary Completion Date

December 19, 2023

Study Completion Date

March 31, 2024

Conditions
Lassa FeverLassa Virus Infection
Interventions
DRUG

rVSV∆G-LASV-GPC

2 × 10\^4 pfu delivered intramuscularly

DRUG

rVSV∆G-LASV-GPC

2 × 10\^5 pfu delivered intramuscularly

DRUG

rVSV∆G-LASV-GPC

2 × 10\^6 pfu delivered intramuscularly

DRUG

rVSV∆G-LASV-GPC

2 × 10\^7 pfu delivered intramuscularly

OTHER

Placebo/Diluent

N/A delivered intramuscularly

Trial Locations (4)

20037

George Washington University, Washington D.C.

96814

East-West Medical Research Institute, Honolulu

02115

Brigham and Women's Hospital, Brookline

Unknown

Redemption Hospital, New Kru Town

Sponsors
All Listed Sponsors
collaborator

George Washington University

OTHER

collaborator

Brigham and Women's Hospital

OTHER

collaborator

Redemption Hospital

UNKNOWN

collaborator

East-West Medical Research Institute

UNKNOWN

lead

International AIDS Vaccine Initiative

NETWORK