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Comparison · NCT04979442-sae

Milademetan vs Trabectedin: serious adverse events

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. Milademetan vs Trabectedin: serious adverse events. Trial comparisons, record NCT04979442-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04979442-sae

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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 10.360.2670.466wilson
Risk in group 20.4810.3740.589wilson
Risk difference, group 1 minus group 2-0.121-0.2640.0295newcombe hybrid score
Risk ratio, group 1 over group 20.7490.5211.08log
Odds ratio, group 1 over group 20.6080.3261.13log
Number needed to treat, for one fewer participant with a serious adverse event on Milademetan than on Trabectedin8.3from 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 1Milademetanmilademetan 260 mg once daily orally on Days 1 to 3 and Days 15 to 17 of each 28-day cycle3186EG000
Group 2Trabectedintrabectedin 1.5 mg/m2 body surface area as a 24-hour IV infusion, every 3 weeks3879EG001

Harm

What it counts
Total, serious adverse events
Time frame
From the first dose date to 30 days after the last dose date or the primary study completion date whichever came first; up to 26.6 months.

Source ClinicalTrials.gov

Trial

Title
Treatment of Milademetan Versus Trabectedin in Patient With Dedifferentiated Liposarcoma
NCT number
NCT04979442
Phases
PHASE3
Conditions
Dedifferentiated Liposarcoma
Interventions
RAIN-32, Trabectedin
Lead sponsor
Rain Oncology Inc
Results first posted
2025-01-14

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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