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:
2025-12-25 @ 1:27 AM
Ignite Modification Date:
2025-12-25 @ 1:27 AM
NCT ID:
NCT02835794
Eligibility Criteria:
Inclusion Criteria:
* Age \>= 18 years;
* Informed consent;
* Low- and intermediate-risk MDS that has failed to achieve any hematologic improvement after at least 4 cycles of induction therapy or has relapsed after any duration of any hematologic response. Prior therapy with azanucleosides (i.e., azacitidine, decitabine), biologic therapies (i.e., lenalidomide, rigosertib) and hematopoietic cell transplant are permissible;
* Performance status must be Eastern Cooperative Oncology Group (ECOG) 0, 1, or 2;
* Women of child-bearing potential (i.e., women who are pre-menopausal or not surgically sterile) may participate, provided they meet the following conditions:
* Must agree to use physician-approved contraceptive methods throughout the study and for three months following the last dose of omacetaxine and
* Must have a negative serum or urine pregnancy test within 7 days prior to beginning treatment on this trial;
* Males with female partners of child-bearing potential must agree to use physician-approved contraceptive methods throughout the study and should avoid conceiving a child for 6 months following the last dose of omacetaxine.
Exclusion Criteria:
* Subjects who are eligible for hematopoietic stem cell transplant;
* History of atrial fibrillation related to azanucleoside therapy in the past;
* Active, uncontrolled, clinically significant infection;
* Pregnant and nursing patients are excluded because the effects of omacetaxine on a fetus or nursing child are unknown;
* Treatment with any anticancer therapy (standard or investigational) within the previous 14 days prior to the first dose of study drug or less than full recovery from the clinically significant toxic effects of that treatment.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02835794
Study Brief:
Protocol Section:
NCT02835794