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Trial · NCT03117309

Results by group15

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

OutcomeGroupCategoryValueSpreadUnits
1-year Progression Free Survival (PFS) Rate for ccRCC PatientsCohort A Part A: Nivolumab Monotherapy in Clear Cell RCCPD-L1 0%34.695% Confidence Interval 24.3 to 45.1Percentage of participants
1-year Progression Free Survival (PFS) Rate for ccRCC PatientsCohort A Part A: Nivolumab Monotherapy in Clear Cell RCCPD-L1 1-5%53.895% Confidence Interval 24.8 to 76.0Percentage of participants
1-year Progression Free Survival (PFS) Rate for ccRCC PatientsCohort A Part A: Nivolumab Monotherapy in Clear Cell RCCPD-L1 5-20%33.395% Confidence Interval 0.9 to 77.4Percentage of participants
1-year Progression Free Survival (PFS) Rate for ccRCC PatientsCohort A Part A: Nivolumab Monotherapy in Clear Cell RCCPD-L1 > 20%7595% Confidence Interval 31.5 to 93.1Percentage of participants
Objective Response Rate for ccRCC Patients Treated With Nivolumab MonotherapyCohort A Part A: Nivolumab Monotherapy in Clear Cell RCCPD-L1 0%26.995% Confidence Interval 17.5 to 38.2Percentage of participants
Objective Response Rate for ccRCC Patients Treated With Nivolumab MonotherapyCohort A Part A: Nivolumab Monotherapy in Clear Cell RCCPD-L1 1-5%53.895% Confidence Interval 25.1 to 80.8Percentage of participants
Objective Response Rate for ccRCC Patients Treated With Nivolumab MonotherapyCohort A Part A: Nivolumab Monotherapy in Clear Cell RCCPD-L1 5-20%33.395% Confidence Interval 0.8 to 90.6Percentage of participants
Objective Response Rate for ccRCC Patients Treated With Nivolumab MonotherapyCohort A Part A: Nivolumab Monotherapy in Clear Cell RCCPD-L1 > 20%7595% Confidence Interval 34.9 to 96.8Percentage of participants
Objective Response Rate (ORR) for ccRCC Patients Treated With Nivolumab and IpilimumabCohort A Part B: Nivolumab and Ipilimumab in Clear Cell RCCPD-L1 0%7.795% Confidence Interval 0.9 to 25.1Percentage of participants
Objective Response Rate (ORR) for ccRCC Patients Treated With Nivolumab and IpilimumabCohort A Part B: Nivolumab and Ipilimumab in Clear Cell RCCPD-L1 1-5%66.795% Confidence Interval 9.4 to 99.2Percentage of participants
Objective Response Rate (ORR) for ccRCC Patients Treated With Nivolumab and IpilimumabCohort A Part B: Nivolumab and Ipilimumab in Clear Cell RCCPD-L1 5-20%095% Confidence Interval NA to NAPercentage of participants
Clinical Activity for nccRCC PatientsCohort B Part A: Nivolumab Monotherapy in Non Clear Cell RCC60Percentage of participants
1-year Progression Free Survival (PFS) Rate for nccRCC PatientsCohort B Part A: Nivolumab Monotherapy in Non Clear Cell RCC25.495% Confidence Interval 14.3 to 45Percentage of participants
Number of Participants With Adverse EventsCohort A: Nivolumab and Salvage Nivolumab/Ipilimumab in Clear Cell RCC128Participants
Number of Participants With Adverse EventsCohort B: Nivolumab and Salvage Nivolumab/Ipilimumab in Non-clear Cell RCC35Participants

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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