Trial to Evaluate the Immunogenicity of Dose Reduction Strategies of the MVA-BN Monkeypox Vaccine

PHASE2CompletedINTERVENTIONAL
Enrollment

229

Participants

Timeline

Start Date

September 9, 2022

Primary Completion Date

October 12, 2023

Study Completion Date

February 24, 2025

Conditions
Monkeypox
Interventions
BIOLOGICAL

JYNNEOS

JYNNEOS is FDA-approved and licensed as a smallpox and monkeypox vaccine in the United States. JYNNEOS is a live vaccine produced from the strain Modified Vaccinia Ankara-Bavarian Nordic (MVA-BN), an attenuated, non-replicating orthopoxvirus. Each 0.5 mL dose is formulated to contain 0.5 x 10\^8 to 3.95 x 10\^8 infectious units of MVA-BN live virus in 10 mM Tris (tromethamine), 140 mM sodium chloride at pH 7.7. Subcutaneous is administered in the deltoid region, intradermal is administered in the volar aspect (inner side) of the forearm.

Trial Locations (8)

20037

George Washington University Medical Faculty Associates, Washington D.C.

30030

The Hope Clinic of Emory University, Decatur

37212

Vanderbilt University Medical Center, Nashville

92103-8208

University of California, San Diego (UCSD) - Antiviral Research Center (AVRC), San Diego

20892-1504

NIH Clinical Research Center, Investigational Drug Management and Research Section, Bethesda

02115-6110

Brigham and Women's Hospital, Boston

63104-1015

Saint Louis University Center for Vaccine Development, St Louis

77030-3411

Baylor College of Medicine, Houston

All Listed Sponsors
lead

National Institute of Allergy and Infectious Diseases (NIAID)

NIH