A Trial to Evaluate the Optimal Dose of MV-LASV (V182-001)

PHASE1CompletedINTERVENTIONAL
Enrollment

60

Participants

Timeline

Start Date

September 26, 2019

Primary Completion Date

March 13, 2020

Study Completion Date

January 15, 2021

Conditions
Lassa Virus Infection
Interventions
BIOLOGICAL

MV-LASV

The MV-LASV vaccine candidate is a recombinant live attenuated viral vectored vaccine, based on the backbone of the measles Schwarz virus strain for prophylaxis of Lassa infection and will be administered in two different dose levels by intra muscular (i.m.) injection.

OTHER

Placebo

A sterile physiological saline solution will be used as placebo to ensure blinding of the treatment with low dose MV-LASV and placebo within treatment group A. Additionally, the Placebo will be used as a control arm to enable comparison of treatment reactions within treatment groups B and C.

Trial Locations (1)

Unknown

University of Antwerpen, Centre for the Evaluation of Vaccination (CEV), Antwerp

Sponsors
All Listed Sponsors
collaborator

Coalition for Epidemic Preparedness Innovations

OTHER

collaborator

Harmony Clinical Research BVBA

OTHER

collaborator

Assign Data Management and Biostatistics GmbH

OTHER

lead

Themis Bioscience GmbH

INDUSTRY