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Comparison · NCT04865289-sae

Lenvatinib + Pembrolizumab vs Paclitaxel + Carboplatin: 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. Lenvatinib + Pembrolizumab vs Paclitaxel + Carboplatin: serious adverse events. Trial comparisons, record NCT04865289-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04865289-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 10.5480.4340.657wilson
Risk in group 20.3040.1990.433wilson
Risk difference, group 1 minus group 20.2440.07180.395newcombe hybrid score
Risk ratio, group 1 over group 21.81.152.83log
Odds ratio, group 1 over group 22.781.345.79log
Number needed to harm, for one more participant with a serious adverse event on Lenvatinib + Pembrolizumab than on Paclitaxel + Carboplatin4.092.5313.9from the risk difference interval

Groups2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Lenvatinib + PembrolizumabParticipants received lenvatinib daily and pembrolizumab once at the start of each 3-week treatment cycle.4073EG000
Group 2Paclitaxel + CarboplatinParticipants received paclitaxel and carboplatin once at the start of each 3-week treatment cycle.1756EG001

Harm

What it counts
Total, serious adverse events
Time frame
From randomization to the date of death or last participant data collection (up to approximately 61 months).

Source ClinicalTrials.gov

Trial

Title
Pembrolizumab (MK-3475) Plus Lenvatinib (E7080/MK-7902) Versus Chemotherapy for Endometrial Carcinoma (ENGOT-en9 / MK-7902-001) - China Extension Study
NCT number
NCT04865289
Phases
PHASE3
Conditions
Endometrial Neoplasms
Interventions
Lenvatinib, Pembrolizumab, Paclitaxel, Carboplatin
Lead sponsor
Merck Sharp & Dohme LLC
Results first posted
2024-10-18

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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