Evaluating the Safety and Immune Response to a Respiratory Syncytial Virus (RSV) Vaccine in Adults, RSV-Seropositive Children, and RSV-Seronegative Infants and Children

PHASE1CompletedINTERVENTIONAL
Enrollment

60

Participants

Timeline

Start Date

August 31, 2011

Primary Completion Date

June 30, 2015

Study Completion Date

August 31, 2015

Conditions
Respiratory Syncytial Virus Infections
Interventions
BIOLOGICAL

RSV MEDI ΔM2-2 vaccine

Given intranasally once at a baseline study visit, at a dose of 10\^5 or 10\^6 plaque-forming units (PFU), depending on study arm.

BIOLOGICAL

Placebo vaccine

Given intranasally once at a baseline study visit

Trial Locations (1)

21205

John Hopkins Center for Immunization Research, Baltimore

All Listed Sponsors
lead

National Institute of Allergy and Infectious Diseases (NIAID)

NIH

NCT01459198 - Evaluating the Safety and Immune Response to a Respiratory Syncytial Virus (RSV) Vaccine in Adults, RSV-Seropositive Children, and RSV-Seronegative Infants and Children | Biotech Hunter | Biotech Hunter