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 @ 11:57 PM
Ignite Modification Date:
2025-12-24 @ 11:57 PM
NCT ID:
NCT00070551
Eligibility Criteria:
Inclusion Criteria:
* Histologically confirmed acute myeloid leukemia according to the WHO classification
* Relapsed or refractory disease, meeting 1 of the following criteria:
* Unresponsive to initial treatment
* Recurrent disease after treatment with prior conventional or high-dose chemotherapy with or without stem cell support
* CNS involvement allowed provided there are no residual leukemic cells detected in the cerebrospinal fluid after intrathecal or radiation chemotherapy
* Performance status - ECOG 0-2
* At least 4 weeks
* Bilirubin no greater than 2 times upper limit of normal\* (ULN) (unless due to Gilbert's syndrome)
* AST and ALT no greater than 3 times ULN\*
* Creatinine no greater than 1.5 mg/dL\*
* No symptomatic congestive heart failure
* No unstable angina pectoris
* No cardiac arrhythmia
* Resting ejection fraction at least 50%\*
* Not pregnant or nursing
* Negative pregnancy test
* Fertile patients must use effective contraception
* No prior allergy to study medications
* No ongoing or active infection requiring IV antibiotics
* No other concurrent uncontrolled illness
* No serious medical or psychiatric illness that would preclude giving informed consent
* More than 4 weeks since prior chemotherapy (except hydroxyurea) (6 weeks for nitrosoureas or mitomycin)
* No other concurrent chemotherapy
* No concurrent hormonal therapy except steroids for adrenal failure and hormones for non-disease-related conditions (e.g., insulin for diabetes)
* More than 4 weeks since prior radiotherapy
* No concurrent palliative radiotherapy
* Prior therapy with antisense oligonucleotides allowed provided no toxic effects were experienced that were directly attributable to the antisense agents
* No other concurrent investigational agents
* No other concurrent anticancer therapy
* No concurrent chronic systemic anticoagulant therapy for medical conditions (e.g., prior deep vein thrombosis or atrial fibrillation)
* Concurrent heparin to maintain central line patency (i.e., catheter flush) is allowed
* No concurrent combination antiretroviral therapy for HIV-positive patients
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT00070551
Study Brief:
Protocol Section:
NCT00070551