5 versionsRe-verified since Apr 24, 2018, no change to tracked fieldsv18-v22
NotableResults first posted: Aug 21, 2013
Primary endpoint revised
v17
MinorEligibility criteria expanded, about 15 words
Study description shortened, about 99 words
v16
MinorTrial status: Active, Not Recruiting to Completed
Enrollment target: estimated 25 to confirmed 17
Primary and study completion dates changed from estimate of Aug 2013 to Nov 2012
v15
Re-verified, no change to tracked fieldsv14
Show 12 earlier versionsHide 12 earlier versions
NotablePrimary and study completion dates: Aug 2012 to Aug 2013v13
Re-verified, no change to tracked fieldsv12
NotablePrimary and study completion dates: Aug 2011 to Aug 2012v11
Re-verified, no change to tracked fieldsv10
NotablePrimary and study completion dates: Aug 2010 to Aug 2011
Study site revised
v9
Re-verified, no change to tracked fieldsv8
MinorTrial status: Recruiting to Active, Not Recruiting
Site details revised
v7
NotablePrimary completion date: Aug 2008 to Aug 2010
Primary endpoint revised
Study completion date: Jul 2009 to Aug 2010
Secondary endpoints shortened, about 7 words
v6
MinorStudy description shortened, about 43 wordsv5
NotablePrimary endpoints: 7 to 1v4Show 5 more changesShow less
Primary completion date: Aug 2008
Study completion date: Jul 2009
Secondary endpoints expanded, about 7 words
Study description expanded, about 86 words
Study arms: 0 to 1
Study Status, Oversight, Study Description, Conditions, Study Design, Eligibility, Contacts/Locationsv3
MinorEligibility criteria expanded, about 64 words
Study description shortened, about 83 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 Chronic Lymphocytic Leukemia (CLL). The safety of the drug will also be studied.
Optional Procedures: You will be asked to have additional blood samples drawn. These samples will be used to see how the disease is responding to the drug.