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Trial · NCT03138512

Results by group274

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

OutcomeGroupCategoryValueSpreadUnits
Disease-Free Survival (DFS) by BICR - Treatment Part A and BTreatment Part A: Nivo + IpiNA95% Confidence Interval NA to NAMonths
Disease-Free Survival (DFS) by BICR - Treatment Part A and BTreatment Part A: PlaceboNA95% Confidence Interval 65.58 to NAMonths
Disease-Free Survival (DFS) by BICR - Treatment Part A and BTreatment Part B: PlaceboNA95% Confidence Interval NA to NAMonths
Disease-Free Survival (DFS) by BICR - Treatment Part A and BTreatment Part B: NivoNA95% Confidence Interval NA to NAMonths
Overall Survival (OS) - Treatment Part A and BTreatment Part A: Nivo + IpiNA95% Confidence Interval NA to NAMonths
Overall Survival (OS) - Treatment Part A and BTreatment Part A: PlaceboNA95% Confidence Interval NA to NAMonths
Overall Survival (OS) - Treatment Part A and BTreatment Part B: PlaceboNA95% Confidence Interval NA to NAMonths
Overall Survival (OS) - Treatment Part A and BTreatment Part B: NivoNA95% Confidence Interval NA to NAMonths
Overall Survival (OS) Rate (5 Years) - Treatment Part A and BTreatment Part A: Nivo + Ipi85.095% Confidence Interval 80.8 to 88.3Percent of participants
Overall Survival (OS) Rate (5 Years) - Treatment Part A and BTreatment Part A: Placebo87.295% Confidence Interval 82.8 to 90.5Percent of participants
Disease-Free Survival (DFS) Per BICR in Contemporaneously Randomized Combination and Monotherapy Participants - Treatment Part BTreatment Part B: Nivo + IpiNA95% Confidence Interval 36.17 to NAMonths
Disease-Free Survival (DFS) Per BICR in Contemporaneously Randomized Combination and Monotherapy Participants - Treatment Part BTreatment Part B: NivoNA95% Confidence Interval NA to NAMonths
Overall Survival (OS) in the Contemporaneously Randomized Combination and Monotherapy Participants - Treatment Part BTreatment Part B: Nivo + IpiNA95% Confidence Interval NA to NAMonths
Overall Survival (OS) in the Contemporaneously Randomized Combination and Monotherapy Participants - Treatment Part BTreatment Part B: NivoNA95% Confidence Interval NA to NAMonths
The Number of Participants With Adverse Events up to 30 Days After Last Dose of Study Therapy - Treatment Part ATreatment Part A: Nivo + IpiAny Grade AE392Participants
The Number of Participants With Adverse Events up to 30 Days After Last Dose of Study Therapy - Treatment Part ATreatment Part A: PlaceboAny Grade AE362Participants
The Number of Participants With Adverse Events up to 30 Days After Last Dose of Study Therapy - Treatment Part ATreatment Part A: Nivo + IpiGrade 3-4 AE154Participants
The Number of Participants With Adverse Events up to 30 Days After Last Dose of Study Therapy - Treatment Part ATreatment Part A: PlaceboGrade 3-4 AE44Participants
The Number of Participants With Adverse Events up to 30 Days After Last Dose of Study Therapy - Treatment Part ATreatment Part A: Nivo + IpiGrade 5 AE1Participants
The Number of Participants With Adverse Events up to 30 Days After Last Dose of Study Therapy - Treatment Part ATreatment Part A: PlaceboGrade 5 AE0Participants

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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GET https://conductscience.org/api/trials/v1/NCT03138512/results