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Trial · NCT03036098

Results by group70

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

OutcomeGroupCategoryValueSpreadUnits
Overall Survival (OS) in Cisplatin-ineligible Randomized Participants for Primary StudyTreatment 119.0695% Confidence Interval 13.47 to 22.60Months
Overall Survival (OS) in Cisplatin-ineligible Randomized Participants for Primary StudyTreatment 213.2195% Confidence Interval 11.63 to 15.24Months
Overall Survival (OS) in Programmed Death-Ligand 1 (PD-L1) Positive (≥ 1%) Randomized Participants by Immunohistochemistry (IHC) for Primary StudyTreatment 116.3095% Confidence Interval 11.53 to 21.82Months
Overall Survival (OS) in Programmed Death-Ligand 1 (PD-L1) Positive (≥ 1%) Randomized Participants by Immunohistochemistry (IHC) for Primary StudyTreatment 214.3695% Confidence Interval 10.48 to 17.64Months
Overall Survival (OS) in All Randomized Participants for Primary StudyTreatment 118.7695% Confidence Interval 15.05 to 21.82Months
Overall Survival (OS) in All Randomized Participants for Primary StudyTreatment 214.3295% Confidence Interval 12.22 to 15.87Months
Progression-Free Survival (PFS) by Blinded Independent Central Review (BICR) [Using Response Evaluation Criteria in Solid Tumors (RECIST) 1.1] in Cisplatin-ineligible Randomized Participants for Primary Study
Treatment 15.2995% Confidence Interval 3.78 to 5.95Months
Progression-Free Survival (PFS) by Blinded Independent Central Review (BICR) [Using Response Evaluation Criteria in Solid Tumors (RECIST) 1.1] in Cisplatin-ineligible Randomized Participants for Primary Study
Treatment 25.8895% Confidence Interval 5.62 to 7.59Months
Progression-Free Survival (PFS) by Blinded Independent Central Review (BICR) [Using Response Evaluation Criteria in Solid Tumors (RECIST) 1.1] in Programmed Death-Ligand 1 (PD-L1) Positive (≥ 1%) Participants for Primary Study
Treatment 15.3995% Confidence Interval 3.75 to 7.39Months
Progression-Free Survival (PFS) by Blinded Independent Central Review (BICR) [Using Response Evaluation Criteria in Solid Tumors (RECIST) 1.1] in Programmed Death-Ligand 1 (PD-L1) Positive (≥ 1%) Participants for Primary Study
Treatment 25.7895% Confidence Interval 4.80 to 6.93Months
Progression-Free Survival (PFS) by Blinded Independent Central Review (BICR) [Using Response Evaluation Criteria in Solid Tumors (RECIST) 1.1] in All Randomized Participants for Primary StudyTreatment 15.0395% Confidence Interval 3.94 to 5.98Months
Progression-Free Survival (PFS) by Blinded Independent Central Review (BICR) [Using Response Evaluation Criteria in Solid Tumors (RECIST) 1.1] in All Randomized Participants for Primary StudyTreatment 26.0195% Confidence Interval 5.78 to 7.52Months
Change From Baseline in the European Organization for Research and Treatment of Care Quality-of-Life Questionnaire (EORTC QLQ-C30) Global Health Status Score in All Randomized Participants for Primary Study
Treatment 1Global Health Status - Baseline63.4Standard Deviation 22.55Score on a Scale
Change From Baseline in the European Organization for Research and Treatment of Care Quality-of-Life Questionnaire (EORTC QLQ-C30) Global Health Status Score in All Randomized Participants for Primary Study
Treatment 2Global Health Status - Baseline59.8Standard Deviation 25.05Score on a Scale
Change From Baseline in the European Organization for Research and Treatment of Care Quality-of-Life Questionnaire (EORTC QLQ-C30) Global Health Status Score in All Randomized Participants for Primary Study
Treatment 1Global Health Status - Week 4-1.1Standard Deviation 18.28Score on a Scale
Change From Baseline in the European Organization for Research and Treatment of Care Quality-of-Life Questionnaire (EORTC QLQ-C30) Global Health Status Score in All Randomized Participants for Primary Study
Treatment 2Global Health Status - Week 42.7Standard Deviation 23.21Score on a Scale
Change From Baseline in the European Organization for Research and Treatment of Care Quality-of-Life Questionnaire (EORTC QLQ-C30) Global Health Status Score in All Randomized Participants for Primary Study
Treatment 1Global Health Status - Week 10-0.5Standard Deviation 23.73Score on a Scale
Change From Baseline in the European Organization for Research and Treatment of Care Quality-of-Life Questionnaire (EORTC QLQ-C30) Global Health Status Score in All Randomized Participants for Primary Study
Treatment 2Global Health Status - Week 103.0Standard Deviation 23.55Score on a Scale
Change From Baseline in the European Organization for Research and Treatment of Care Quality-of-Life Questionnaire (EORTC QLQ-C30) Global Health Status Score in All Randomized Participants for Primary Study
Treatment 1Global Health Status - Week 163.6Standard Deviation 22.59Score on a Scale
Change From Baseline in the European Organization for Research and Treatment of Care Quality-of-Life Questionnaire (EORTC QLQ-C30) Global Health Status Score in All Randomized Participants for Primary Study
Treatment 2Global Health Status - Week 163.1Standard Deviation 24.68Score on a Scale

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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