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NCT05127434 A Study to Evaluate the Safety and Efficacy of mRNA-1345 Vaccine Targeting Respiratory Syncytial Virus (RSV) in Adults ≥60 Years of Age Status COMPLETED Phase PHASE2/PHASE3
NCT04978337 A Study of Rilematovir (JNJ-53718678) in Adult Outpatients With Respiratory Syncytial Virus (RSV) Infection Status TERMINATED Phase PHASE2
NCT04528719 A Dose Escalation Study to Evaluate Safety, Reactogenicity, and Immunogenicity of mRNA-1345 in Healthy Adults and in Children Who Are Respiratory Syncytial Virus (RSV)-Seropositive Status COMPLETED Phase PHASE1
NCT04221412 Pre-Approval Access to JNJ-53718678 for the Treatment of Respiratory Syncytial Virus (RSV) Infection in (a) Immunocompromised Adult and Pediatric Participants Status NO_LONGER_AVAILABLE Phase N/A
NCT04196101 A Study to Assess EDP-938 for the Treatment of Acute Upper Respiratory Tract Infection With Respiratory Syncytial Virus in Adult Subjects Status COMPLETED Phase PHASE2
NCT03606512 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 Status COMPLETED Phase PHASE1/PHASE2
NCT03524118 Safety, Tolerability, and Pharmacokinetics of Clesrovimab (MK-1654) in Infants (MK-1654-002) Status COMPLETED Phase PHASE1/PHASE2
NCT03049488 Dose, Safety, Tolerability and Immunogenicity of a Stabilized Prefusion RSV F Subunit Protein Vaccine, VRC-RSVRGP084-00-VP (DS-Cav1), Alone or With Alum Adjuvant, in Healthy Adults Status COMPLETED Phase PHASE1
NCT02707523 Prospective Pilot Clinical Trial of Azithromycin Treatment In Respiratory Syncytial Virus (RSV)- Induced Respiratory Failure In Children Status COMPLETED Phase PHASE2
NCT02508194 A Study to Evaluate the Efficacy of MEDI7510 in Older Adults Status TERMINATED Phase PHASE2
NCT02472548 A Study to Evaluate the Safety and Reactogenicity of DPX-RSV(A), a Respiratory Syncytial Virus Vaccine Status COMPLETED Phase PHASE1
NCT02290340 A Phase 1b/2a Randomized, Double-Blind, Placebo-controlled, Dose-escalation Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of MEDI8897, a Monoclonal Antibody With an Extended Half-life Against Respiratory Syncytial Virus, in Healthy Preterm Infants Status COMPLETED Phase PHASE1
NCT02254408 Presatovir in Hematopoietic Cell Transplant Recipients With Respiratory Syncytial Virus Infection of the Upper Respiratory Tract Status COMPLETED Phase PHASE2
NCT02133092 A Study in Belgian Children Hospitalized With Respiratory Syncytial Virus Related Acute Respiratory Infections Status COMPLETED Phase N/A
NCT02132923 A Study in Japanese Children Hospitalized With Respiratory Syncytial Virus Related Lower Respiratory Tract Infections Status COMPLETED Phase N/A
NCT01995175 A Prospective, Epidemiological Study to Assess the Disease Burden of Respiratory Syncytial Virus Associated, Suspected Lower Respiratory Tract Infections in Newborns, From 0 to 2 Years of Age and Risk of Development of Wheeze and Asthma From 0 to 6 Years of Age Status COMPLETED Phase NA