NotableResults first posted: Jan 15, 2026v63Show 7 more changesShow less
Primary endpoints: 2 to 1
Enrollment target: 156 to 150
Interventions: Dasatinib (Drug), Laboratory Biomarker Analysis (Other), Pharmacological Study (Other), Quality-of-Life Assessment (Other), Questionnaire… to Dasatinib (Drug)
Secondary endpoints expanded, about 14 words
Study description expanded, about 117 words
Study arms: 2 to 1
Eligibility criteria shortened, about 2 words
Re-verified, no change to tracked fieldsv62
MinorTrial status: Active, Not Recruiting to Completed
Primary and study completion dates changed from estimate of Nov 30, 2024 to Mar 14, 2025
v61
6 versionsRe-verified since Dec 6, 2022, no change to tracked fieldsv55-v60
NotablePrimary and study completion dates: Nov 30, 2022 to Nov 30, 2024v54
Show 40 earlier versionsHide 40 earlier versions
NotablePrimary completion date: Nov 30, 2021 to Nov 30, 2022v53
NotablePrimary completion date: Nov 30, 2020 to Nov 30, 2021
Enrollment target: estimated 150 to confirmed 156
Study completion date: Nov 30, 2020 to Nov 30, 2022
v52
NotablePrimary and study completion dates: Nov 30, 2019 to Nov 30, 2020
Eligibility criteria shortened, about 12 words
v51
MinorStudy description revised
Collaborators: 2 to 1
v50
Re-verified, no change to tracked fieldsv49
NotablePrimary endpoints: 1 to 2v48Show 8 more changesShow less
Primary and study completion dates: Nov 2019 to Nov 30, 2019
Start date: Nov 2005 to Nov 8, 2005
Interventions: Dasatinib (BMS-354825) (Drug) to Dasatinib (Drug), Laboratory Biomarker Analysis (Other), Pharmacological Study (Other), Quality-of-Life Assessment (Other), Questionnaire…
Eligibility criteria expanded, about 13 words
Study description shortened, about 112 words
Study site revised
Collaborators: 1 to 2
Study title expanded, about 2 words
Re-verified, no change to tracked fieldsv47
MinorEligibility criteria revisedv46
Re-verified, no change to tracked fieldsv45
NotablePrimary completion date: Nov 2018 to Nov 2019
Study completion date: Nov 2019
v44
Re-verified, no change to tracked fieldsv43
NotablePrimary completion date: Nov 2017 to Nov 2018
Eligibility criteria revised
v42
NotablePrimary completion date: Nov 2016 to Nov 2017
Study completion date: Nov 2016 to not stated
v41
Re-verified, no change to tracked fieldsv40
MinorStudy description revised
Eligibility criteria expanded, about 5 words
v39
3 versionsRe-verified since Sep 11, 2014, no change to tracked fieldsv36-v38
MinorTrial status: Recruiting to Active, Not Recruiting
Study site revised
v35
NotablePrimary and study completion dates: Nov 2015 to Nov 2016v34
MinorStudy description shortened, about 1 wordv33
3 versionsRe-verified since Dec 3, 2013, no change to tracked fieldsv30-v32
MinorStudy description shortened, about 4 wordsv29
NotableTrial status: Active, Not Recruiting to Recruiting
Site details revised
v28
MinorTrial status: Recruiting to Active, Not Recruiting
Site details revised
v27
MinorEligibility criteria revisedv26
NotablePrimary and study completion dates: Nov 2014 to Nov 2015
Eligibility criteria shortened, about 2 words
v25
Re-verified, no change to tracked fieldsv24
MinorEligibility criteria expanded, about 2 wordsv23
MinorEligibility criteria shortened, about 29 wordsv22
Re-verified, no change to tracked fieldsv21
NotablePrimary and study completion dates: Nov 2012 to Nov 2014
Eligibility criteria expanded, about 4 words
v20
2 versionsRe-verified since Nov 4, 2011, no change to tracked fieldsv18-v19
MinorEligibility criteria expanded, about 1 wordv17
MinorEligibility criteria expanded, about 35 words
Study description shortened, about 114 words
v16
NotablePrimary and study completion dates: Nov 2011 to Nov 2012v15
NotablePrimary and study completion dates pushed to Nov 2011v14
Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The goal of this clinical research study is to learn if BMS-354825 (dasatinib) can help to control CML in chronic phase. The safety of this drug will also be studied.