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Trial · NCT01227421

Outcomes15

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYTime to Resolution of All Clinical Symptoms of Influenza as Reported by the SubjectsUp to 28 days624 patients were enrolled based on inclusion/exclusion criteria. The primary efficacy analysis was conducted on the 257 patients with laboratory confirmed influenza.HoursMEDIAN
SECONDARYTime to Resolution of Each Individual Symptom of Influenza as Reported by the Subjectsat least 28 days624 patients were enrolled based on inclusion/exclusion criteria. Secondary efficacy analyses were conducted on the 257 patients with laboratory confirmed influenza.HoursMEDIAN
SECONDARYMean Change (Standard Deviation)in 50% Tissue Culture Infective Dose (TCID50) Viral Titer From Baseline7 daysAnalysis conducted on 113 patients from intensive virologic follow up group with laboratory confirmed influenzaLOG10 TiterMEAN
SECONDARYMean Change in RT-PCR (Reverse Transcription Polymerase Chain Reaction) Viral Titer From Baseline7 daysAnalysis conducted on 113 patients from the intensive virologic follow up group with laboratory confirmed influenzaLOG10 RNA copiesMEAN
SECONDARYTime to Cessation of Viral Shedding Measure by 50% Tissue Culture Infective Dose (TCID50)28 daysAnalysis performed on 107 patients from the intensive virologic follow up population with laboratory confirmed influenzaHoursMEDIAN
SECONDARYTime to Return to Normal Daily Activities28 daysAnalysis conducted on 257 patients with laboratory confirmed influenzaHoursMEDIAN
SECONDARYSymptom Severity Score Hours28 daysAnalysis conducted for 257 patients with laboratory confirmed influenzasymptom score *hourMEAN
SECONDARYTime Loss From Work28 daysAnalysis conducted on 241 patients with laboratory confirmed influenza excluding those who are unemployeddaysMEAN
SECONDARYComplications of Influenza28 daysAll patients who received at least one dose of study medicationParticipantsNUMBER
SECONDARYInfluenza Antibody Response Titer Change: Influenza A 2009 H1N128 daysMember of the intensive virologic follow up group with laboratory confirmed Influenza A 2009 H1N1Fold change in antibody titerMEDIAN
SECONDARYInfluenza Antibody Response: Influenza A H3N228 daysMembers of the intensive virologic follow up group with laboratory confirmed influenza A H3N2Fold change in antibody titerMEDIAN
SECONDARYInfluenza Antibody Response: Influenza B28 daysMembers of intensive virologic follow up group with laboratory confirmed Influenza BFold change in antibody titerMEDIAN
SECONDARYInfluenza Antibody Response: Seroprotection and Seroconversion for Patients With Influenza A 2009 H1N128 daysMembers of intensive virologic follow up group with laboratory confirmed Influenza A 2009 H1N1ParticipantsNUMBER
SECONDARYInfluenza Antibody Response: Seroprotection and Seroconversion for Patients With Influenza A H3N228 daysMembers of intensive virologic follow up group with laboratory confirmed Influenza A H3N2ParticipantsNUMBER
SECONDARYInfluenza Antibody Response: Seroprotection and Seroconversion for Influenza B28 daysMembers of intensive virologic follow up group with laboratory confirmed Influenza BParticipantsNUMBER

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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