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Trial · NCT02488759

Results by group93

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

OutcomeGroupCategoryValueSpreadUnits
Neoadjuvant: Number of Participants With Drug-Related Select Adverse Events (AEs)NeoadjuvantEndocrine AEs3Participants
Neoadjuvant: Number of Participants With Drug-Related Select Adverse Events (AEs)NeoadjuvantGastrointestinal AEs4Participants
Neoadjuvant: Number of Participants With Drug-Related Select Adverse Events (AEs)NeoadjuvantHepatic AEs3Participants
Neoadjuvant: Number of Participants With Drug-Related Select Adverse Events (AEs)NeoadjuvantPulmonary AEs0Participants
Neoadjuvant: Number of Participants With Drug-Related Select Adverse Events (AEs)NeoadjuvantRenal AEs0Participants
Neoadjuvant: Number of Participants With Drug-Related Select Adverse Events (AEs)NeoadjuvantSkin AEs9Participants
Neoadjuvant: Number of Participants With Drug-Related Select Adverse Events (AEs)NeoadjuvantHypersensitivity/Infusion Reaction AEs5Participants
Neoadjuvant: Number of Participants With Drug-Related Serious Adverse Events (SAEs)Neoadjuvant6Participants
Neoadjuvant: Rate of Surgery DelayNeoadjuvantHPV positive SCCHN095% Confidence Interval 0 to 13.7Percentage of participants
Neoadjuvant: Rate of Surgery DelayNeoadjuvantHPV negative SCCHN095% Confidence Interval 0 to 13.7Percentage of participants
Neoadjuvant: Rate of Surgery DelayNeoadjuvantCervical Carcinoma7.795% Confidence Interval 0.2 to 36.0Percentage of participants
Neoadjuvant: Rate of Surgery DelayNeoadjuvantVaginal/Vulvar Carcinoma095% Confidence Interval 0.0 to 26.5Percentage of participants
Neoadjuvant: Rate of Surgery DelayNeoadjuvantMerkel Cell Carcinoma2.795% Confidence Interval 0.1 to 14.2Percentage of participants
Metastatic: Investigator-Assessed Objective Response Rate (ORR)Metastatic MonotherapyEBV positive related gastric cancer14.395% Confidence Interval 1.8 to 42.8Percentage of participants
Metastatic: Investigator-Assessed Objective Response Rate (ORR)Metastatic MonotherapyHPV positive SCCHN11.595% Confidence Interval 2.4 to 30.2Percentage of participants
Metastatic: Investigator-Assessed Objective Response Rate (ORR)Metastatic Combo AHPV positive SCCHN31.095% Confidence Interval 17.6 to 47.1Percentage of participants
Metastatic: Investigator-Assessed Objective Response Rate (ORR)Metastatic Combo CHPV positive SCCHN095% Confidence Interval 0.0 to 36.9Percentage of participants
Metastatic: Investigator-Assessed Objective Response Rate (ORR)Metastatic Combo AOther anogenital HPV associated cancers34.895% Confidence Interval 16.4 to 57.3Percentage of participants
Metastatic: Investigator-Assessed Objective Response Rate (ORR)Metastatic Combo BOther anogenital HPV associated cancers28.695% Confidence Interval 11.3 to 52.2Percentage of participants
Metastatic: Investigator-Assessed Objective Response Rate (ORR)Metastatic Combo DSCCHN I-O naive16.795% Confidence Interval 0.4 to 64.1Percentage of participants

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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