3 versionsRe-verified since Mar 31, 2023, no change to tracked fieldsv26-v28
NotableResults first posted: May 6, 2019
Secondary endpoints: details revised at 1 of 1 entry
Study arms: 1 to 5
Eligibility criteria expanded, about 2 words
v25
NotablePrimary completion date: Dec 2007 to Mar 3, 2017v24Show 4 more changesShow less
Trial status: Active, Not Recruiting to Completed
Enrollment target: estimated 145 to confirmed 68
Study completion date changed from estimate of Nov 2018 to Mar 3, 2017
Start date: Nov 2005 to Nov 15, 2005
MinorPrimary completion date changed from estimate of Nov 2018 to Dec 2007
Study completion date: Nov 2018
v23
NotablePrimary completion date: Nov 2016 to Nov 2018v22
Show 20 earlier versionsHide 20 earlier versions
NotablePrimary completion date: Nov 2015 to Nov 2016
Secondary endpoints: details revised at 1 of 1 entry
v21
NotablePrimary completion date: Nov 2014 to Nov 2015v20
Re-verified, no change to tracked fieldsv19
NotablePrimary endpoint revised
Eligibility criteria expanded, about 8 words
v18
Re-verified, no change to tracked fieldsv17
NotablePrimary completion date: Nov 2012 to Nov 2014v16
Re-verified, no change to tracked fieldsv15
MinorStudy description expanded, about 15 wordsv14
NotablePrimary completion date: Nov 2011 to Nov 2012
Study description shortened, about 118 words
v13
NotablePrimary completion date: Nov 2010 to Nov 2011v12
2 versionsRe-verified since Jul 26, 2010, no change to tracked fieldsv10-v11
NotablePrimary completion date: Dec 2009 to Nov 2010v9Show 5 more changesShow less
Primary endpoint revised
Study completion date: Dec 2009 to not stated
Eligibility criteria shortened, about 16 words
Secondary endpoint revised
Study description shortened, about 144 words
MinorPrimary completion date: Dec 2009
Study completion date: Aug 2009 to Dec 2009
Secondary endpoints: details revised at 1 of 1 entry
v8
NotablePrimary endpoints: 3 to 1v7Show 7 more changesShow less
Trial status: Recruiting to Active, Not Recruiting
Study sites: 2 to 1
Study completion date: Aug 2009
Interventions: dasatinib (BMS-354825) (Drug) to Dasatinib (BMS-354825) (Drug)
Secondary endpoints expanded, about 7 words
Study description expanded, about 124 words
Study arms: 0 to 1
2 versionsRe-verified since Oct 23, 2006, no change to tracked fieldsv5-v6
MinorEnrollment target: 120 to 145
Study description expanded, about 156 words
v4
Re-verified, no change to tracked fieldsv3
MinorInterventions: desatinib (BMS-354825) (Drug) to dasatinib (BMS-354825) (Drug)
Eligibility criteria expanded, about 21 words
Study description revised
Study title expanded, about 2 words
v2
Study First Submitted
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 dasatinib can help to control myeloproliferative disorders. The safety and tolerability of dasatinib will also be studied.