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Trial · NCT04117945

Adverse event totals12

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityArm A (Regorafenib)412
Total, all-cause mortalityArm B (Cetuximab, Panitumumab, Irinotecan)610
Total, all-cause mortalityCrossover From Arm A24
Total, all-cause mortalityCrossover From Arm B68
Total, other adverse eventsArm A (Regorafenib)1212
Total, other adverse eventsArm B (Cetuximab, Panitumumab, Irinotecan)910
Total, other adverse eventsCrossover From Arm A44
Total, other adverse eventsCrossover From Arm B78
Total, serious adverse eventsArm A (Regorafenib)612
Total, serious adverse eventsArm B (Cetuximab, Panitumumab, Irinotecan)410
Total, serious adverse eventsCrossover From Arm A14
Total, serious adverse eventsCrossover From Arm B18

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
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
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this list from software.

Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT04117945/event-totals