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Comparison · NCT04214860-deaths

Cohort 1 vs Cohort 2: 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. Cohort 1 vs Cohort 2: deaths from any cause. Trial comparisons, record NCT04214860-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04214860-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 110.611wilson
Risk in group 20.6050.4560.736wilson
Risk difference, group 1 minus group 20.395-0.01660.544newcombe hybrid score
Risk ratio, group 1 over group 21.651.32.11log
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zero
Number needed to harm, for one more death from any cause on Cohort 1 than on Cohort 22.53from 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 1Cohort 1APR-246 4.5 g/day~APR-246: APR-246 4.5 g/day~Venetoclax: Venetoclax 400 mg once daily66EG000
Group 2Cohort 2APR-246 4.5 g/day~APR-246: APR-246 4.5 g/day~Venetoclax: Venetoclax 400 mg once daily~Azacitidine: Subcutaneous injection, or intravenous infusion2643EG001

Harm

What it counts
Total, all-cause mortality
Time frame
18 months

Source ClinicalTrials.gov

Trial

Title
APR-246 in Combination With Venetoclax and Azacitidine in TP53-Mutant Myeloid Malignancies
NCT number
NCT04214860
Phases
PHASE1
Conditions
Myeloid Malignancy
Interventions
APR-246, Venetoclax, Azacitidine
Lead sponsor
Aprea Therapeutics
Results first posted
2025-02-21

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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