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Trial · NCT01218516

Results by group18

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Progression-free Survival (PFS)Combination Therapy: Placebo + ChemotherapyPer Primary Analysis Cut-Off Date5.895% Confidence Interval 5.0 to 6.8Months
Progression-free Survival (PFS)Combination Therapy: Farletuzumab + ChemotherapyPer Primary Analysis Cut-Off Date4.795% Confidence Interval 4.2 to 5.6Months
Progression-free Survival (PFS)Combination Therapy: Placebo + ChemotherapyPer Final Analysis Cut-Off Date5.995% Confidence Interval 5.0 to 7.0Months
Progression-free Survival (PFS)Combination Therapy: Farletuzumab + ChemotherapyPer Final Analysis Cut-Off Date4.795% Confidence Interval 4.2 to 5.6Months
Overall Response Rate (ORR)Combination Therapy: Placebo + Chemotherapy37.3Percentage of participants
Overall Response Rate (ORR)Combination Therapy: Farletuzumab + Chemotherapy41.3Percentage of participants
Duration of Response (DR)Combination Therapy: Placebo + Chemotherapy6.795% Confidence Interval 4.1 to 9.4Months
Duration of Response (DR)Combination Therapy: Farletuzumab + Chemotherapy4.195% Confidence Interval 3.0 to 7.0Months
Overall Survival (OS)Combination Therapy: Placebo + Chemotherapy10.595% Confidence Interval 8.3 to 14.0Months
Overall Survival (OS)Combination Therapy: Farletuzumab + Chemotherapy14.195% Confidence Interval 9.5 to 18.6Months
Number of Participants With Treatment-Emergent Adverse Events (TEAEs) and Treatment-Emergent Serious Adverse Events (SAEs)Combination Therapy: Placebo + ChemotherapyTEAEs60Participants
Number of Participants With Treatment-Emergent Adverse Events (TEAEs) and Treatment-Emergent Serious Adverse Events (SAEs)Combination Therapy: Farletuzumab + ChemotherapyTEAEs63Participants
Number of Participants With Treatment-Emergent Adverse Events (TEAEs) and Treatment-Emergent Serious Adverse Events (SAEs)Monotherapy: PlaceboTEAEs30Participants
Number of Participants With Treatment-Emergent Adverse Events (TEAEs) and Treatment-Emergent Serious Adverse Events (SAEs)Monotherapy: FarletuzumabTEAEs25Participants
Number of Participants With Treatment-Emergent Adverse Events (TEAEs) and Treatment-Emergent Serious Adverse Events (SAEs)Combination Therapy: Placebo + ChemotherapyTreatment emergent SAEs27Participants
Number of Participants With Treatment-Emergent Adverse Events (TEAEs) and Treatment-Emergent Serious Adverse Events (SAEs)Combination Therapy: Farletuzumab + ChemotherapyTreatment emergent SAEs27Participants
Number of Participants With Treatment-Emergent Adverse Events (TEAEs) and Treatment-Emergent Serious Adverse Events (SAEs)Monotherapy: PlaceboTreatment emergent SAEs6Participants
Number of Participants With Treatment-Emergent Adverse Events (TEAEs) and Treatment-Emergent Serious Adverse Events (SAEs)Monotherapy: FarletuzumabTreatment emergent SAEs7Participants

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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