Study of a Respiratory Syncytial Virus Candidate Encapsulated in a Lipid Nanoparticle Based Formulation in Adults Aged 18 to 50 Years and 60 Years and Older

Last updated:
2026-09-12
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View trial details

Overview

Official protocol title:

A PHASE I/II, RANDOMIZED, PLACEBO-CONTROLLED MULTI-ARM DOSE-FINDING STUDY TO EVALUATE THE SAFETY AND IMMUNOGENICITY OF A RESPIRATORY SYNCYTIAL VIRUS (RSV) MRNA VACCINE CANDIDATE WITH EITHER LNP CL-0059 OR LNP CL0137 IN ADULT PARTICIPANTS 18 TO 50 YEARS OF AGE IN A SENTINEL COHORT AND 60 YEARS AND OLDER IN MAIN AND BOOSTER COHORTS

Intervention/treatment:
569 - RESPIRATORY SYNCYTIAL VIRUS MRNA VACCINE (MRT5600 AND MRT5601)
Medical condition:
RESPIRATORY SYNCYTIAL VIRUS
Protocol code:
VAE00010
Control number:
269245
Status:
Closed
Approved:
December 01, 2022
Date Completed:
Trial phase:
Phase 1, Phase 2
For more information:
ClinicalTrials.gov - NCT05639894
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
18 Years and older
Accepts healthy volunteers: Yes

Contacts and locations

Contact
Name
Trial Transparency Team
Organization
Sanofi Pasteur
Phone:
800-633-1610
Extension 6#
Sponsor
SANOFI PASTEUR INC

Results

See the results from the trial NCT05639894. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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