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Trial · NCT01018563

Results by group18

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

OutcomeGroupCategoryValueSpreadUnits
Duration of Ovarian Tumor Marker (Cancer Antigen 125 [CA125]) ResponseFarletuzumab 62.5 mg/m^2Participant 1 (dose group: 62.5 mg/m^2)-C77.2months
Duration of Ovarian Tumor Marker (Cancer Antigen 125 [CA125]) ResponseFarletuzumab 62.5 mg/m^2Participant 2 (dose group: 62.5 mg/m^2)-C73.3months
Duration of Ovarian Tumor Marker (Cancer Antigen 125 [CA125]) ResponseFarletuzumab 100 mg/m^2Participant 3 (dose group: 100 mg/m^2)18.0months
Progression-Free Survival (PFS) by GCIGFarletuzumab 62.5 mg/m^2Participant 1 (dose group: 62.5 mg/m^2)-C: GCIG77.8months
Progression-Free Survival (PFS) by GCIGFarletuzumab 62.5 mg/m^2Participant 2 (dose group: 62.5 mg/m^2)-C: GCIG75.8months
Progression-Free Survival (PFS) by GCIGFarletuzumab 100 mg/m^2Participant 3 (dose group: 100 mg/m^2): GCIG25.1months
Overall Survival (OS)Farletuzumab 62.5 mg/m^2Participant 1 (dose group: 62.5 mg/m^2)-C78.3months
Overall Survival (OS)Farletuzumab 62.5 mg/m^2Participant 2 (dose group: 62.5 mg/m^2)-C76.7months
Overall Survival (OS)Farletuzumab 100 mg/m^2Participant 3 (dose group: 100 mg/m^2)59.5months
Duration of Second RemissionFarletuzumab 62.5 mg/m^2Participant 1 (dose group: 62.5 mg/m^2)41.0months
Duration of Second RemissionFarletuzumab 62.5 mg/m^2Participant 2 (dose group: 62.5 mg/m^2)-C74.2months
Duration of Second RemissionFarletuzumab 100 mg/m^2Participant 3 (dose group: 100 mg/m^2)29.5months
Duration of Third RemissionFarletuzumab 62.5 mg/m^237.3months
Duration of Third RemissionFarletuzumab 100 mg/m^225.0months
Number of Participants With Best Overall Response as Evaluated by Response Evaluation Criteria in Solid Tumors (RECIST) V.1.0 CriteriaFarletuzumab 62.5 mg/m^2CR1Participants
Number of Participants With Best Overall Response as Evaluated by Response Evaluation Criteria in Solid Tumors (RECIST) V.1.0 CriteriaFarletuzumab 100 mg/m^2CR1Participants
Number of Participants With Best Overall Response as Evaluated by Response Evaluation Criteria in Solid Tumors (RECIST) V.1.0 CriteriaFarletuzumab 62.5 mg/m^2SD1Participants
Number of Participants With Best Overall Response as Evaluated by Response Evaluation Criteria in Solid Tumors (RECIST) V.1.0 CriteriaFarletuzumab 100 mg/m^2SD0Participants

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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