A Study to Evaluate the Safety, Reactogenicity, and Immunogenicity of Adenovirus Serotype 26 Based Respiratory Syncytial Virus Pre-fusion (Ad26.RSV.Pre-F) Vaccine in RSV-Seronegative Toddlers 12 to 24 Months of Age

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

A RANDOMIZED, CONTROLLED, OBSERVER-BLIND, PHASE 1/2A STUDY TO EVALUATE THE SAFETY, REACTOGENICITY, AND IMMUNOGENICITY OF AD26.RSV.PREF IN RSV-SERONEGATIVE TODDLERS 12 TO 24 MONTHS OF AGE

Intervention/treatment:
JNJ-64400141 (AD26.RSV.PREF)
Medical condition:
RESPIRATORY SYNCYTIAL VIRUS
Protocol code:
VAC18194RSV2002
Control number:
223810
Status:
Closed
Approved:
February 15, 2019
Date Completed:
Trial phase:
Phase 1, Phase 2
For more information:
ClinicalTrials.gov - NCT03606512
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
12 Months to 24 Months
Accepts healthy volunteers: Yes

Contacts and locations

Contact
Name
Clinical Franchise Leader
Organization
Janssen Vaccines & Prevention B.V
Phone:
844-434-4210
Sponsor
JANSSEN INC

Locations

Nova Scotia

Dalhousie University
Halifax, Nova Scotia, B3K 6R8

Ontario

Children's Hospital of Eastern Ontario
Ottawa, Ontario, K1H 8L1

Quebec

CHU de Quebec Universite Laval
Québec, Quebec, G1V 4G2
McGill University Health Centre - Vaccine Study Centre
Pierrefonds, Quebec, H9H 4Y6

Results

See the results from the trial NCT03606512. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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