Phase 1/2 Study of Respiratory Syncytial Virus and Human Metapneumovirus (RSV+HMPV) Vaccine Candidate in Adults 60 Years of Age and Older
Recruiting
Phase 1
Phase 2
Interventional Study
Respiratory Syncytial Virus Immunization
Human Metapneumovirus Immunization
Healthy Volunteers
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 60 and older
- Sex
- Any
- Trial phase
- Phase 1/2
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 2,400 (estimated)
- Sponsor
- Sanofi · Industry
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About This Trial
This study is a Phase 1/2, randomized, observer-blind, active and placebo-controlled, multi-center study to be conducted in approximately 2400 adults 60 years of age and older. The aim of the study is to evaluate the immunogenicity and safety of an RSV+HMPV vaccine candidate for the prevention of RSV and HMPV disease among adults 60 years of age and older. While there are 3 FDA approved/licensed R…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Aged 60 years or older on the day of inclusion
* Non-childbearing potential (ie, post-menopausal for at least 1 year or surgically sterile)
Exclusion Criteria:
* History of laboratory-confirmed RSV and/or laboratory-confirmed HMPV infection affecting the participant and/or t…
Contacts
Trial Transparency email recommended (Toll free for US & Canada)
800-633-1610
CONTACT