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Study identifier: NCT07158814 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Safety of RSV Preventive Monoclonal Antibody

Condition: Fever · Adverse Event Following Immunisation  ·  Sponsor: Duke University

PhasePhase 4
Planned participants524
Who can joinAll sexes, 6 Weeks to 30 Weeks
Healthy volunteersYes

About this study

This is a prospective, randomized, open-label clinical trial to evaluate the safety of administration of respiratory syncytial virus (RSV) preventive monoclonal antibody and other routine childhood vaccines given simultaneously at Visit 1, as compared to sequential administration of respiratory syncytial virus (RSV) preventive monoclonal antibody and other vaccines at separate visits (Visits 1 and 2).

This description comes directly from the study's public registry record.

Talk to the study team

Michael J Smith, MD  ·  919 684 6335  ·  michael.j.smith@duke.edu

Emily A Randolph, MBA  ·  919 385 5785  ·  emily.randolph@duke.edu

Always discuss trial participation with your own doctor first.

Locations (6)

Kaiser Permanente Northern CaliforniaOakland, California, United StatesRecruiting
Emory UniversityAtlanta, Georgia, United StatesRecruiting
Centers for Disease Control and PreventionAtlanta, Georgia, United StatesActive Not Recruiting
Columbia UniversityNew York, New York, United StatesRecruiting
Duke UniversityDurham, North Carolina, United StatesRecruiting
Cincinnati Children's Hospital Medical CenterCincinnati, Ohio, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07158814