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Comparison · NCT01198067-sae

Cohort 2 vs Cohort 3: 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. Cohort 2 vs Cohort 3: serious adverse events. Trial comparisons, record NCT01198067-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01198067-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 110.4391wilson
Risk in group 20.1670.03010.564wilson
Risk difference, group 1 minus group 20.8330.1460.97newcombe hybrid score
Risk ratio, group 1 over group 26135.9log
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zero
Number needed to harm, for one more participant with a serious adverse event on Cohort 2 than on Cohort 31.21.036.86from 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 1Cohort 22mg Pomolidomide per day per Cycle (Cycle = 28 days)33EG000
Group 2Cohort 31mg Pomolidomide per day per Cycle (Cycle = 28 days)16EG001

Harm

What it counts
Total, serious adverse events
Time frame
All Adverse Events were collected through Study Completion (Avg. 1 Year)

Source ClinicalTrials.gov

Trial

Title
Pomalidomide in Treating Patients With Relapsed or Refractory Waldenstrom Macroglobulinemia
NCT number
NCT01198067
Phases
PHASE1
Conditions
Recurrent Waldenstrom Macroglobulinemia, Refractory Waldenstrom Macroglobulinemia
Interventions
Pomalidomide
Lead sponsor
M.D. Anderson Cancer Center
Results first posted
2025-09-04

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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