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Trial · NCT02470585

Results by group180

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

OutcomeGroupCategoryValueSpreadUnits
Progression-Free Survival (PFS) in the BRCA-deficient Population (Arm 3 vs Arm 1)Placebo + Carboplatin + Paclitaxel -> Placebo22.095% Confidence Interval 17.8 to 29.1months
Progression-Free Survival (PFS) in the BRCA-deficient Population (Arm 3 vs Arm 1)Veliparib + Carboplatin + Paclitaxel -> Placebo21.195% Confidence Interval 17.0 to 25.5months
Progression-Free Survival (PFS) in the BRCA-deficient Population (Arm 3 vs Arm 1)Veliparib + Carboplatin + Paclitaxel -> Veliparib34.795% Confidence Interval 31.8 to NAmonths
Progression-Free Survival (PFS) in the Homologous Recombination Deficiency Cohort (Arm 3 vs Arm 1)Placebo + Carboplatin + Paclitaxel -> Placebo20.595% Confidence Interval 17.8 to 22.8months
Progression-Free Survival (PFS) in the Homologous Recombination Deficiency Cohort (Arm 3 vs Arm 1)Veliparib + Carboplatin + Paclitaxel -> Placebo18.195% Confidence Interval 16.4 to 22.7months
Progression-Free Survival (PFS) in the Homologous Recombination Deficiency Cohort (Arm 3 vs Arm 1)Veliparib + Carboplatin + Paclitaxel -> Veliparib31.995% Confidence Interval 25.8 to 38.0months
Progression-Free Survival (PFS) in the Intention-to-treat Population (Arm 3 vs Arm 1)Placebo + Carboplatin + Paclitaxel -> Placebo17.395% Confidence Interval 15.1 to 19.1months
Progression-Free Survival (PFS) in the Intention-to-treat Population (Arm 3 vs Arm 1)Veliparib + Carboplatin + Paclitaxel -> Placebo15.295% Confidence Interval 14.1 to 17.3months
Progression-Free Survival (PFS) in the Intention-to-treat Population (Arm 3 vs Arm 1)Veliparib + Carboplatin + Paclitaxel -> Veliparib23.595% Confidence Interval 19.3 to 26.3months
Progression-Free Survival (PFS) in the BRCA-deficient Population (Arm 2 vs Arm 1)Placebo + Carboplatin + Paclitaxel -> Placebo22.095% Confidence Interval 17.8 to 29.1months
Progression-Free Survival (PFS) in the BRCA-deficient Population (Arm 2 vs Arm 1)Veliparib + Carboplatin + Paclitaxel -> Placebo21.195% Confidence Interval 17.0 to 25.5months
Progression-Free Survival (PFS) in the BRCA-deficient Population (Arm 2 vs Arm 1)Veliparib + Carboplatin + Paclitaxel -> Veliparib34.795% Confidence Interval 31.8 to NAmonths
Progression-Free Survival (PFS) in the Homologous Recombination Deficiency Cohort (Arm 2 vs Arm 1)Placebo + Carboplatin + Paclitaxel -> Placebo20.595% Confidence Interval 17.8 to 22.8months
Progression-Free Survival (PFS) in the Homologous Recombination Deficiency Cohort (Arm 2 vs Arm 1)Veliparib + Carboplatin + Paclitaxel -> Placebo18.195% Confidence Interval 16.4 to 22.7months
Progression-Free Survival (PFS) in the Homologous Recombination Deficiency Cohort (Arm 2 vs Arm 1)Veliparib + Carboplatin + Paclitaxel -> Veliparib31.995% Confidence Interval 25.8 to 38.0months
Progression-Free Survival (PFS) in the Intention-to-treat Population (Arm 2 vs Arm 1)Placebo + Carboplatin + Paclitaxel -> Placebo17.395% Confidence Interval 15.1 to 19.1months
Progression-Free Survival (PFS) in the Intention-to-treat Population (Arm 2 vs Arm 1)Veliparib + Carboplatin + Paclitaxel -> Placebo15.295% Confidence Interval 14.1 to 17.3months
Progression-Free Survival (PFS) in the Intention-to-treat Population (Arm 2 vs Arm 1)Veliparib + Carboplatin + Paclitaxel -> Veliparib23.595% Confidence Interval 19.3 to 26.3months
Overall Survival (OS) in the BRCA-deficient PopulationPlacebo + Carboplatin + Paclitaxel -> Placebo89.595% Confidence Interval 83.3 to NAmonths
Overall Survival (OS) in the BRCA-deficient PopulationVeliparib + Carboplatin + Paclitaxel -> PlaceboNA95% Confidence Interval 69.3 to NAmonths

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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