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Comparison · NCT01830621-sae

BBI608 vs Placebo: 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. BBI608 vs Placebo: serious adverse events. Trial comparisons, record NCT01830621-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01830621-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 10.2940.2240.376wilson
Risk in group 20.2010.1440.274wilson
Risk difference, group 1 minus group 20.0927-0.008370.192newcombe hybrid score
Risk ratio, group 1 over group 21.460.9632.22log
Odds ratio, group 1 over group 21.650.9542.86log
Number needed to harm, for one more participant with a serious adverse event on BBI608 than on Placebo10.8from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1BBI608BBI608 480 mg two times daily (960 mg total daily dose)+ Best Supportive Care~BBI608~Best Supportive Care~At risk patients included only patients who received at least one dose of BBI60840136EG000
Group 2PlaceboPlacebo two times daily + Best Supportive Care~Placebo~Best Supportive Care~At risk patients included only patients who received at least one dose of placebo29144EG001

Harm

What it counts
Total, serious adverse events
Time frame
36 months

Source ClinicalTrials.gov

Trial

Title
BBI608 and Best Supportive Care vs Placebo and Best Supportive Care in Pretreated Advanced Colorectal Carcinoma
NCT number
NCT01830621
Phases
PHASE3
Conditions
Colorectal Carcinoma
Interventions
BBI608, Placebo, Best Supportive Care
Lead sponsor
NCIC Clinical Trials Group
Results first posted
2019-03-11

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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