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NCT03106779 · OUTCOME

Time to Complete Cytogenetic Response Rate (CCyR) Among Participants Who Achieved CCyR

Study of Efficacy of CML-CP Patients Treated With ABL001 Versus Bosutinib, Previously Treated With 2 or More TKIs · Source last updated 2026-08-18

Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.

Measure
MEDIAN
Unit
Weeks
Interval / dispersion
Full Range
Time frame
216 Weeks

What was measured

Time to CCyR was defined as the time from the date of randomization to the date of the first documented CCyR.

Analysis population: CCyR responder set was a subset of FAS and included patients who did not have CCyR at baseline and achieved CCyR at any time on randomized treatment. FAS comprised of all randomized participants.

Groups in this outcome

Asciminib

Participants randomized to asciminib 40mg BID

Bosutinib

Participants randomized to bosutinib 500mg QD

Group identifiers and denominators belong to this outcome only. They may differ in another outcome or in safety reporting.

Analysis denominator · Participants

GroupSource count
Asciminib52
Bosutinib22

Reported measurements

Source class 1
Values in Weeks · Interval/dispersion: Full Range
GroupValueSpreadLowerUpperComment
Asciminib24.3Not reported23216Not reported
Bosutinib24.3Not reported1253Not reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        lower Limit
        23
        upper Limit
        216
        value
        24.3
      2. group Id
        OG001
        lower Limit
        12
        upper Limit
        53
        value
        24.3
denoms
  1. counts
    1. group Id
      OG000
      value
      52
    2. group Id
      OG001
      value
      22
    units
    Participants
description
Time to CCyR was defined as the time from the date of randomization to the date of the first documented CCyR.
dispersion Type
Full Range
groups
  1. description
    Participants randomized to asciminib 40mg BID
    id
    OG000
    title
    Asciminib
  2. description
    Participants randomized to bosutinib 500mg QD
    id
    OG001
    title
    Bosutinib
param Type
MEDIAN
population Description
CCyR responder set was a subset of FAS and included patients who did not have CCyR at baseline and achieved CCyR at any time on randomized treatment. FAS comprised of all randomized participants.
reporting Status
POSTED
time Frame
216 Weeks
title
Time to Complete Cytogenetic Response Rate (CCyR) Among Participants Who Achieved CCyR
type
SECONDARY
unit Of Measure
Weeks

Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0

Preserved source evidence · Not medical advice