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Trial · NCT07895394

Registered outcomes13

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryHumoral immune response (neutralizing antibody)1 month after vaccinationGeometric mean fold rise (GMFR) in RSV-A neutralizing antibody titers from pre-vaccination to 1 month after vaccination, compared between lung transplant recipients and immunocompetent adults.
SecondaryHumoral immune response (neutralizing antibody)Prevaccination, 1 month and 12 months after vaccinationGeometric mean titers (GMTs) in RSV-A neutralizing antibody titers
SecondaryHumoral immune response (neutralizing antibody)Prevaccination, 1 month and 12 months after vaccinationGeometric mean titers (GMTs) in RSV-B neutralizing antibody titers
SecondaryHumoral immune response (neutralizing antibody)1 month, 12 months after vaccinationGeometric mean fold rises (GMFRs) in RSV-A neutralizing antibody titers from pre-vaccination levels.
SecondaryHumoral immune response (neutralizing antibody)1 month, 12 months after vaccinationGeometric mean fold rises (GMFRs) in RSV-B neutralizing antibody titers from pre-vaccination levels.
SecondaryHumoral immune response (RSV specific antibody)Prevaccination, 1 month and 12 months after vaccinationGeometric mean concentrations (GMCs) in RSVPreF3-specific IgG
SecondaryHumoral immune response (RSV specific antibody)Prevaccination, 1 month and 12 months after vaccinationGeometric mean concentrations (GMCs) in pan-RSV-specific IgG
SecondaryHumoral immune response (RSV specific antibody)1 month, 12 months after vaccinationGeometric mean fold rises (GMFRs) in RSVPreF3-specific IgG from pre-vaccination levels.
SecondaryHumoral immune response (RSV specific antibody)1 month, 12 months after vaccinationGeometric mean fold rises (GMFRs) in pan-RSV-specific IgG from pre-vaccination levels.
SecondaryHumoral immune response (serologic response rate)1 month, 12 months after vaccinationProportion of participants with a ≥4-fold increase in antibody levels from pre-vaccination levels
SecondaryCell mediated immunity1 month, 12 months after vaccinationFrequency of RSV F-specific CD4+ and CD8+ T cells following stimulation with RSV F peptide pools, measured by flow cytometry.
SecondarySafety (solicited adverse events)7 days, 30 days after vaccinationProportion of participants experiencing solicited local and systemic adverse events following vaccination.
SecondarySafety (unsolicited adverse events, serious adverse events)Up to 12 months after vaccinationProportion of participants experiencing unsolicited adverse events or serious adverse events following vaccination.

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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