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Comparison · NCT01650805-17246cb2

Ponatinib vs Imatinib: Complete Cytogenetic Response (CCyR) Rate

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. Ponatinib vs Imatinib: Complete Cytogenetic Response (CCyR) Rate. Trial comparisons, record NCT01650805-17246cb2. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01650805-17246cb2

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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 110.5661wilson
Risk in group 20.8570.4870.974wilson
Risk difference, group 1 minus group 20.143-0.3070.513newcombe hybrid score
Risk ratio, group 1 over group 21.170.8621.58log
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zero
Number needed to treat, for one more participant with the outcome on Ponatinib than on Imatinib7from 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 1Ponatinibponatinib: 45 mg tablet, taken orally once daily55OG000
Group 2Imatinibimatinib (Gleevec/ Glivec): 400 mg tablet, taken orally once daily67OG001

Outcome

Type
SECONDARY
Title
Complete Cytogenetic Response (CCyR) Rate
Description
The percentage of Ph+ metaphases in bone marrow (peripheral blood may not be used), with a review of a minimum of 20 metaphases. Responses are defined as follows: Complete (CCyR): 0% Ph+ metaphases.
Time frame
12 months after first dose
Population
Patients with 12 month assessment

Source ClinicalTrials.gov

Trial

Title
Ponatinib in Newly Diagnosed Chronic Myeloid Leukemia (CML) (EPIC)
NCT number
NCT01650805
Phases
PHASE3
Conditions
Chronic Myeloid Leukemia
Interventions
ponatinib, imatinib (Gleevec/ Glivec)
Lead sponsor
Ariad Pharmaceuticals
Results first posted
2014-10-21

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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