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Comparison · NCT04865289-e227ecb4

Lenvatinib + Pembrolizumab vs Paclitaxel + Carboplatin: Number of Participants Experiencing an Adverse Event (AE)

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: Number of Participants Experiencing an Adverse Event (AE). Trial comparisons, record NCT04865289-e227ecb4. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04865289-e227ecb4

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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 10.9860.9260.998wilson
Risk in group 210.9361wilson
Risk difference, group 1 minus group 2-0.0137-0.07360.0515newcombe hybrid score
Risk ratio, group 1 over group 20.9860.961.01log
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zero
Number needed to treat, for one fewer participant with the outcome on Lenvatinib + Pembrolizumab than on Paclitaxel + Carboplatin73from 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 1Lenvatinib + PembrolizumabParticipants received lenvatinib daily and pembrolizumab once at the start of each 3-week treatment cycle.7273OG000
Group 2Paclitaxel + CarboplatinParticipants received paclitaxel and carboplatin once at the start of each 3-week treatment cycle.5656OG001

Outcome

Type
SECONDARY
Title
Number of Participants Experiencing an Adverse Event (AE)
Description
An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of study intervention, whether or not considered related to the study intervention.
Time frame
From first dose date to 120 days after last dose date (up to approximately 58 months)
Population
All Chinese participants who were randomized to the global study (NCT03884101) and to the extension portion and received at least one dose of the study intervention were analyzed

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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