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Comparison · NCT03552380-deaths

Phase II, Dose Level 1: Entinostat 5 mg With Nivolumab and Ipilimumab vs Phase II, Dose Level 2: Entinostat 3 mg With Nivolumab and Ipilimumab: deaths from any cause

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Phase II, Dose Level 1: Entinostat 5 mg With Nivolumab and Ipilimumab vs Phase II, Dose Level 2: Entinostat 3 mg With Nivolumab and Ipilimumab: deaths from any cause. Trial comparisons, record NCT03552380-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03552380-deaths

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.60.2310.882wilson
Risk in group 20.5710.250.842wilson
Risk difference, group 1 minus group 20.0286-0.4290.456newcombe hybrid score
Risk ratio, group 1 over group 21.050.4022.75log
Odds ratio, group 1 over group 21.130.10911.6log
Number needed to harm, for one more death from any cause on Phase II, Dose Level 1: Entinostat 5 mg With Nivolumab and Ipilimumab than on Phase II, Dose Level 2: Entinostat 3 mg With Nivolumab and Ipilimumab
35from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Phase II, Dose Level 1: Entinostat 5 mg With Nivolumab and Ipilimumab
Patients received oral entinostat at a dose of 5 mg every 7 days continuously with nivolumab at a dose of 3 mg/kg mg IV every three weeks in combination with ipilimumab at a dose of 1 mg/kg every 3 weeks X 4 doses. Then, nivolumab 480 mg was continued every 4 weeks.
35EG000
Group 2Phase II, Dose Level 2: Entinostat 3 mg With Nivolumab and Ipilimumab
Patients received oral entinostat at a dose of 3 mg every 7 days continuously with nivolumab at a dose of 3 mg/kg mg IV every three weeks in combination with ipilimumab at a dose of 1 mg/kg every 3 weeks X 4 doses. Then, nivolumab 480 mg was continued every 4 weeks.
47EG001

Harm

What it counts
Total, all-cause mortality
Time frame
All-Cause Mortality was monitored up to a maximum of 59 months. Serious Adverse Events and Other (Not Including Serious) Adverse Events were monitored up to 31 months.

Source ClinicalTrials.gov

Trial

Title
Study of Entinostat With Nivolumab Plus Ipilimumab in Previously Treated Renal Cell Carcinoma
NCT number
NCT03552380
Phases
PHASE2
Conditions
Renal Cell Carcinoma
Interventions
Entinostat, Nivolumab, Ipilimumab
Lead sponsor
Roberto Pili
Results first posted
2024-09-03

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
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

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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