Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 4:44 PM
Ignite Modification Date:
2025-12-24 @ 4:44 PM
NCT ID:
NCT00852566
Eligibility Criteria:
Inclusion Criteria:
* Patients are able to provide written informed consent
* Patients must have CML in CP which is defined by the presence of all of the following criteria:
* \< 15% blasts in peripheral blood (PB) and BM.
* \< 30% blasts plus promyelocytes in PB and BM.
* \< 20% basophils in the PB.
* ≥ 100 x 109/L platelets.
* No evidence of extramedullary leukemia apart from hepatosplenomegaly
* Ph+ or variants must be demonstrated by BM cytogenetics, FISH or PCR.
* Previously untreated CML in CP, with the exception of hydroxyurea or anagrelide
* Patients must be enrolled in this study within 90 days after the date of first being diagnosed with CML
* ECOG Performance Status (PS) Score 0 - 1 (see Appendix 2)
* Adequate hepatic function defined as: total bilirubin ≤ 2.0 times the institutional upper limit of normal (ULN) in absence of Gilbert type unconjugated hyperbilirubinemia; alanine aminotransferase (ALAT≤ 2.5 times the institutional ULN.
* Adequate renal function defined as serum creatinine ≤ 2 times the institutional ULN.
* Men and women, ages 18 years and older.
* Adequate BM aspiration sample before the start of study treatment (i.e sample is sufficient for stem cell analysis)
* Potentially fertile women must use an adequate method of contraception to avoid pregnancy throughout the study.
* Potentially fertile women must have a negative serum or urine pregnancy test
Exclusion Criteria:
* Fertile women who are unwilling or unable to use an acceptable method to avoid pregnancy for the entire study
* Women who are pregnant or breastfeeding.
* Men with fertile sexual partners who can or will not use an acceptable contraception method for the entire study
* A serious uncontrolled medical disorder or active infection that would impair the ability of the subject to receive protocol therapy.
* Known pleural effusion at baseline.
* Uncontrolled or significant cardiovascular disease
* History of significant bleeding disorder unrelated to CML, including:
* Prior chemotherapy for peripheral stem cell mobilization.
* Inadequate BM aspiration sample due to marrow fibrosis or other reasons
* Prior or concurrent malignancy
* Severe psychiatric illness, imprisonment or mental impairment inflicting on ability to give informed consent
* Abuse of alcohol, prescribed or illicit drugs
* Evidence of digestive dysfunction that would prevent administration of study therapy by mouth.
* Prohibited Treatments and/or Therapies
* Any prior treatment with interferon
* Any prior treatment with dasatinib
* Any prior treatment with imatinib
* Any other prior systemic treatments, with anti-CML activity \[except for anagrelide, or hydroxyurea (HU)\].
* Patients currently taking drugs that are generally accepted to have a risk of causing Torsades de Pointes as described in Appendix 3.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT00852566
Study Brief:
Protocol Section:
NCT00852566