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Comparison · NCT02152631-sae

Abemaciclib vs Erlotinib: 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. Abemaciclib vs Erlotinib: serious adverse events. Trial comparisons, record NCT02152631-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02152631-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 10.4230.3650.483wilson
Risk in group 20.2460.1880.315wilson
Risk difference, group 1 minus group 20.1770.0870.26newcombe hybrid score
Risk ratio, group 1 over group 21.721.282.31log
Odds ratio, group 1 over group 22.251.473.43log
Number needed to harm, for one more participant with a serious adverse event on Abemaciclib than on Erlotinib5.653.8411.5from 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 1Abemaciclib200 mg abemaciclib administered, orally, every 12 hours plus BSC on Days 1 to 28 (28 day cycles).112265EG000
Group 2Erlotinib150 mg erlotinib administered, orally, every 24 hours plus BSC on Days 1 to 28 (28 day cycles).43175EG001

Harm

What it counts
Total, serious adverse events
Time frame
From Baseline to End of Study (Up to 47 Months)

Source ClinicalTrials.gov

Trial

Title
A Study of Abemaciclib (LY2835219) in Participants With Previously Treated KRAS Mutated Lung Cancer
NCT number
NCT02152631
Phases
PHASE3
Conditions
Non Small Cell Lung Cancer
Interventions
Abemaciclib, Erlotinib
Lead sponsor
Eli Lilly and Company
Results first posted
2018-12-12

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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GET https://conductscience.org/api/comparisons/v1/NCT02152631-sae