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Trial · NCT02506153

Results by group276

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

OutcomeGroupCategoryValueSpreadUnits
Overall Survival (OS)FDA Approved Regimen (SOC)7695% Confidence Interval 73 to 80percentage of participants
Overall Survival (OS)MK-3475 (Pembrolizumab)8295% Confidence Interval 78 to 84percentage of participants
Relapse-free Survival (RFS)FDA Approved Regimen (SOC)4995% Confidence Interval 45 to 53percentage of participants
Relapse-free Survival (RFS)MK-3475 (Pembrolizumab)5895% Confidence Interval 54 to 62percentage of participants
Overall Survival (OS) in Participants Who Are PD-L1 PositiveFDA Approved Regimen (SOC)7995% Confidence Interval 74 to 82percentage of participants
Overall Survival (OS) in Participants Who Are PD-L1 PositiveMK-3475 (Pembrolizumab)8395% Confidence Interval 80 to 86percentage of participants
Relapse-free Survival (RFS) in Participants Who Are PD-L1 PositiveFDA Approved Regimen (SOC)5195% Confidence Interval 46 to 55percentage of participants
Relapse-free Survival (RFS) in Participants Who Are PD-L1 PositiveMK-3475 (Pembrolizumab)6095% Confidence Interval 56 to 64percentage of participants
Number of Participants With Gr 3 Through 5 Adverse Events That Are Related to Study DrugsFDA Approved RegimenAbdominal pain6Participants
Number of Participants With Gr 3 Through 5 Adverse Events That Are Related to Study DrugsMK-3475 (Pembrolizumab)Abdominal pain2Participants
Number of Participants With Gr 3 Through 5 Adverse Events That Are Related to Study DrugsFDA Approved RegimenAcidosis1Participants
Number of Participants With Gr 3 Through 5 Adverse Events That Are Related to Study DrugsMK-3475 (Pembrolizumab)Acidosis2Participants
Number of Participants With Gr 3 Through 5 Adverse Events That Are Related to Study DrugsFDA Approved RegimenAcute kidney injury2Participants
Number of Participants With Gr 3 Through 5 Adverse Events That Are Related to Study DrugsMK-3475 (Pembrolizumab)Acute kidney injury2Participants
Number of Participants With Gr 3 Through 5 Adverse Events That Are Related to Study DrugsFDA Approved RegimenAdrenal insufficiency9Participants
Number of Participants With Gr 3 Through 5 Adverse Events That Are Related to Study DrugsMK-3475 (Pembrolizumab)Adrenal insufficiency4Participants
Number of Participants With Gr 3 Through 5 Adverse Events That Are Related to Study DrugsFDA Approved RegimenAlanine aminotransferase increased44Participants
Number of Participants With Gr 3 Through 5 Adverse Events That Are Related to Study DrugsMK-3475 (Pembrolizumab)Alanine aminotransferase increased19Participants
Number of Participants With Gr 3 Through 5 Adverse Events That Are Related to Study DrugsFDA Approved RegimenAlkaline phosphatase increased3Participants
Number of Participants With Gr 3 Through 5 Adverse Events That Are Related to Study DrugsMK-3475 (Pembrolizumab)Alkaline phosphatase increased0Participants

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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