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Study on a Live-attenuated Respiratory Syncytial Virus Vaccine for Assessment of Safety, Transmissibility, and Genetic Stability of the Vaccine Virus Among Close Contacts in Infants and Toddlers 6 to < 24 Months of Age in Puerto Rico (USA)

Completed · Phase 1, Phase 2 · NCT05687279

Conditions: Respiratory Syncytial Virus Infection

At a glance

Research payments reported, 2025
$147,404
U.S. investigators named
5
Sites paid
4
Planned or actual enrollment
80

About the trial

Sponsor
Sanofi Pasteur, a Sanofi Company
Tested
RSVt Vaccine (biological), Control Group (other)
Dates
Started 2023-02-06; completion 2024-12-27
Results posted
Yes

The primary purpose of the study is to assess the shedding, transmission, and genetic stability of the live-attenuated RSVt vaccine after each intranasal vaccination (56 days apart) in infants and toddlers 6 to \< 24 months of age.

From ClinicalTrials.gov, last updated 2026-01-26. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Sanofi Pasteur Inc. reported $147,404 in research payments for this study in 2025 (10 payments).

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

  • Clinical Research Investigator Group Llc $52,874
  • Clinical Research Puerto Rico,inc $45,449
  • Velocity Clinical Research,inc $32,000
  • Caribbean Medical Research Center Llc $17,081

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.