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Trial · NCT02546375

Outcomes19

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYPercentage of Participants With Cumulative Complete Haematological Response (CHR)Baseline up to 5.5 years
All enrolled participants with Philadephia chromosome positive CML in chronic phase received at least 1 dose of Bosutinib. Here, number of participants analyzed (N) signifies those participants who were evaluable for this outcome measure.
percentage of participantsNUMBER
PRIMARYPercentage of Participants With Cumulative Partial Haematological Response (PHR)Baseline up to 5.5 years
All enrolled participants with Philadephia chromosome positive CML in chronic phase received at least 1 dose of Bosutinib. Here, N signifies those participants who were evaluable for this outcome measure.
percentage of participantsNUMBER
PRIMARYPercentage of Participants With Cumulative Complete Cytogenetic Response (CCyR)Baseline up to 5.5 years
All enrolled participants with Philadephia chromosome positive CML in chronic phase received at least 1 dose of Bosutinib. Here, N signifies those participants who were evaluable for this outcome measure.
percentage of participantsNUMBER
PRIMARYPercentage of Participants With Cumulative Minor Cytogenetic Response (MCyR)Baseline up to 5.5 years
All enrolled participants with Philadephia chromosome positive CML in chronic phase received at least 1 dose of Bosutinib. Here, N signifies those participants who were evaluable for this outcome measure.
percentage of participantsNUMBER
PRIMARYPercentage of Participants With Cumulative Minimal Cytogenetic Response (mCyR)Baseline up to 5.5 years
All enrolled participants with Philadephia chromosome positive CML in chronic phase received at least 1 dose of Bosutinib. Here, N signifies those participants who were evaluable for this outcome measure.
percentage of participantsNUMBER
PRIMARYPercentage of Participants With Cumulative Partial Cytogenetic Response (PCyR)Baseline up to 5.5 years
All enrolled participants with Philadephia chromosome positive CML in chronic phase received at least 1 dose of Bosutinib. Here, N signifies those participants who were evaluable for this outcome measure.
percentage of participantsNUMBER
PRIMARYPercentage of Participants With Cumulative Complete Molecular Response 4.0 (MR4.0)Baseline up to 5.5 years
All enrolled participants with Philadephia chromosome positive CML in chronic phase received at least 1 dose of Bosutinib. Here, N signifies those participants who were evaluable for this outcome measure.
percentage of participantsNUMBER
PRIMARYPercentage of Participants With Cumulative Complete Molecular Response 4.5 (MR4.5)Baseline up to 5.5 years
All enrolled participants with Philadephia chromosome positive CML in chronic phase received at least 1 dose of Bosutinib. Here, N signifies those participants who were evaluable for this outcome measure.
percentage of participantsNUMBER
PRIMARYPercentage of Participants With Cumulative Major Molecular Response (MMR)/Molecular Response 3.0 (MR3.0)Baseline up to 5.5 years
All enrolled participants with Philadephia chromosome positive CML in chronic phase received at least 1 dose of Bosutinib. Here, N signifies those participants who were evaluable for this outcome measure.
percentage of participantsNUMBER
SECONDARYPercentage of Participants With Treatment Related Adverse Events (AEs)Baseline up to 5.5 yearsAll enrolled participants with Philadephia chromosome positive CML in chronic phase received at least 1 dose of Bosutinib.percentage of participantsNUMBER
SECONDARYPercentage of Participants With Treatment Related Adverse Events (AEs) Greater Than or Equal to Grade 3Baseline up to 5.5 yearsAll enrolled participants with Philadephia chromosome positive CML in chronic phase received at least 1 dose of Bosutinib.percentage of participantsNUMBER
SECONDARYProgression-free Survival (PFS)Year 1, 2, 3All enrolled participants with Philadephia chromosome positive CML in chronic phase received at least 1 dose of Bosutinib.yearsMEDIAN
SECONDARYOverall Survival (OS)From baseline up to 1 Year, baseline up to Year 2, baseline up to Year 3All enrolled participants with Philadephia chromosome positive CML in chronic phase received at least 1 dose of Bosutinib.yearsMEDIAN
SECONDARYPercentage of Participants With Disease ProgressionYear 1, 2, 3
All enrolled participants with Philadephia chromosome positive CML in chronic phase received at least 1 dose of Bosutinib. Here, N signifies those participants who were evaluable for this outcome measure and number analyzed (n) signifies those participants who were evaluable at specified time points only.
percentage of participantsNUMBER
SECONDARYPercentage of Participants With Permanent Discontinuation From Bosutinib TherapyBaseline up to 5.5 yearsAll enrolled participants with Philadephia chromosome positive CML in chronic phase received at least 1 dose of Bosutinib.percentage of participantsNUMBER
SECONDARYCross-Intolerance Between Bosutinib and Previous TherapyBaseline up to 5.5 yearsAll enrolled participants with Philadephia chromosome positive CML in chronic phase received at least 1 dose of Bosutinib.percentage of participantsNUMBER
SECONDARYMean Dose of Bosutinib at Initiation of TreatmentBaseline up to 5.5 yearsAll enrolled participants with Philadephia chromosome positive CML in chronic phase received at least 1 dose of Bosutinib.milligram per dayMEAN
SECONDARYRelative Bosutinib Dose IntensityBaseline up to 5.5 yearsAll enrolled participants with Philadephia chromosome positive CML in chronic phase received at least 1 dose of Bosutinib.percentage of daily doseNUMBER
SECONDARYDuration of Bosutinib TherapyBaseline up to 5.5 yearsAll enrolled participants with Philadephia chromosome positive CML in chronic phase received at least 1 dose of Bosutinib.monthsMEDIAN

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.

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