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Comparison · NCT01001377-sae

Cetuximab vs Panitumumab: 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. Cetuximab vs Panitumumab: serious adverse events. Trial comparisons, record NCT01001377-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01001377-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 10.3360.2960.378wilson
Risk in group 20.3040.2660.346wilson
Risk difference, group 1 minus group 20.0315-0.02630.0891newcombe hybrid score
Risk ratio, group 1 over group 21.10.9211.32log
Odds ratio, group 1 over group 21.160.8861.51log
Number needed to harm, for one more participant with a serious adverse event on Cetuximab than on Panitumumab31.7from 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 1CetuximabCetuximab 400 mg/m\^2 as an initial dose, followed by 250 mg/m\^2 intravenously (IV) every 7 days.169503EG000
Group 2PanitumumabPanitumumab 6 mg/kg IV every 14 days.151496EG001

Harm

What it counts
Total, serious adverse events
Time frame
Median time was 117 days for panitumumab arm and 123 days for cetuximab arm.

Source ClinicalTrials.gov

Trial

Title
ASPECCT: A Study of Panitumumab Efficacy and Safety Compared to Cetuximab in Patients With KRAS Wild-Type Metastatic Colorectal Cancer
NCT number
NCT01001377
Phases
PHASE3
Conditions
Metastatic Colorectal Cancer
Interventions
Cetuximab, Panitumumab
Lead sponsor
Amgen
Results first posted
2014-03-24

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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