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Trial · NCT02915523

Results by group37

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

OutcomeGroupCategoryValueSpreadUnits
Phase 2: Progression Free Survival (PFS), as Determined by the Local Investigator Using Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST 1.1)Phase 2: Avelumab + Placebo1.5195% Confidence Interval 1.45 to 2.50months
Phase 2: Progression Free Survival (PFS), as Determined by the Local Investigator Using Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST 1.1)Phase 2: Avelumab + Entinostat1.6495% Confidence Interval 1.41 to 2.69months
Phase 1b: Number of Participants With at Least One Dose Limiting Toxicity (DLT) Adverse Event (AE)Phase 1B: Avelumab + Entinostat (3 mg)0Participants
Phase 1b: Number of Participants With at Least One Dose Limiting Toxicity (DLT) Adverse Event (AE)Phase 1B: Avelumab + Entinostat (5 mg)1Participants
Phase 1b: Recommended Phase 2 Dose (RP2D)Phase 1B: Avelumab + Entinostat5mg
Phase 2: PFS, as Determined by the Local Investigator Using Immune Response RECIST (irRECIST)Phase 2: Avelumab + Placebo2.1095% Confidence Interval 1.45 to 2.79months
Phase 2: PFS, as Determined by the Local Investigator Using Immune Response RECIST (irRECIST)Phase 2: Avelumab + Entinostat1.7795% Confidence Interval 1.45 to 2.69months
Phase 2: Objective Response Rate (ORR), as Assessed Using RECIST 1.1Phase 2: Avelumab + Placebo4.8895% Confidence Interval 0.60 to 16.53percentage of participants
Phase 2: Objective Response Rate (ORR), as Assessed Using RECIST 1.1Phase 2: Avelumab + Entinostat5.8895% Confidence Interval 1.94 to 13.20percentage of participants
Phase 2: ORR, as Assessed Using irRECISTPhase 2: Avelumab + Placebo2.4495% Confidence Interval 0.06 to 12.86percentage of participants
Phase 2: ORR, as Assessed Using irRECISTPhase 2: Avelumab + Entinostat4.7195% Confidence Interval 1.30 to 11.61percentage of participants
Phase 2: Clinical Benefit Rate (CBR), as Assessed Using RECIST 1.1Phase 2: Avelumab + Placebo9.7695% Confidence Interval 2.72 to 23.13percentage of participants
Phase 2: Clinical Benefit Rate (CBR), as Assessed Using RECIST 1.1Phase 2: Avelumab + Entinostat11.7695% Confidence Interval 5.79 to 20.57percentage of participants
Phase 2: CBR, as Assessed Using irRECISTPhase 2: Avelumab + Placebo9.7695% Confidence Interval 2.72 to 23.13percentage of participants
Phase 2: CBR, as Assessed Using irRECISTPhase 2: Avelumab + Entinostat9.4195% Confidence Interval 4.15 to 17.71percentage of participants
Phase 2: Overall SurvivalPhase 2: Avelumab + Placebo10.5595% Confidence Interval 6.41 to 16.72months
Phase 2: Overall SurvivalPhase 2: Avelumab + Entinostat12.8595% Confidence Interval 9.53 to 18.37months
Phase 2: Duration of ResponsePhase 2: Avelumab + Placebo6.8395% Confidence Interval 4.14 to NAmonths
Phase 2: Duration of ResponsePhase 2: Avelumab + Entinostat4.2195% Confidence Interval 2.17 to 16.59months
Phase 2: Time to ResponsePhase 2: Avelumab + Placebo2.1095% Confidence Interval 1.38 to 2.83months

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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