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 @ 10:29 PM
Ignite Modification Date:
2025-12-24 @ 10:29 PM
NCT ID:
NCT02485535
Eligibility Criteria:
Inclusion Criteria:
* Signed, written informed consent in accordance with federal, local, and institutional guidelines
* Patients underwent allo-SCT with intermediate risk and high risk AML and high risk MDS (defined by American Society for Blood and Marrow Transplantation \[ASBMT\] criteria), who are within 60 to 100 days after allo-SCT
* There is no evidence of disease relapse at the time of screening, and minimal residual disease (MRD) is acceptable
* Eastern Cooperative Oncology Group (ECOG) performance status of =\< 2
* Absolute neutrophil count (ANC) \> 1000 uL
* Platelets \>= 20,000 without platelet transfusion
* Creatinine clearance \> 30 cc/min calculated using the Cockcroft and Gault (1976) formula or measured
* Total bilirubin =\< 2 mg/dl unless high indirect bilirubin is due to a congenital disorder
* Transaminases (aspartate aminotransferase \[AST\] or alanine aminotransferase \[ALT\]) =\< 2.0 x upper limit of normal (ULN)
* Prothrombin time (PT) and partial thromboplastin time (PTT) =\< 2 x ULN
* Willingness and ability to comply with scheduled visits, treatment plans, laboratory tests and other study procedures
* It is important patients understand the need to use birth control while on this study; female patients of child-bearing potential must agree to use dual methods of contraception and have a negative serum pregnancy test at screening (\< 3 days prior to first dose), male patients with partners of childbearing potential must agree to use effective contraception during the study period and a period of 3 months after the last dose of study drug; for both male and female patients, effective methods of contraception must be used throughout the study and for three months following the last dose
Exclusion Criteria:
* Patients with acute GVHD grade II-IV
* Treatment with any investigational agent within three weeks prior to first dose in this study
* Major surgery within 2 weeks of first dose of study drug; patients must have recovered from the effects of any surgery performed greater than 2 weeks previously
* Patient has a concurrent active malignancy under treatment
* Unstable cardiovascular function:
* Symptomatic ischemia, or
* Uncontrolled clinically significant conduction abnormalities (i.e., ventricular tachycardia on antiarrhythmic agents are excluded; 1st degree atrioventricular (AV) block or asymptomatic left anterior fascicular block/right bundle branch block (LAFB/RBBB) will not be excluded), or
* Congestive heart failure (CHF) NYHA class \>= 3, or
* Myocardial infarction (MI) within 3 months
* Uncontrolled infection requiring parenteral antibiotics, antivirals, or antifungals within one week prior to first dose; infections controlled on concurrent anti-microbial agents are acceptable, and anti-microbial prophylaxis per institutional guidelines are acceptable
* Known active hepatitis B virus (HBV) or C virus (HCV) infection; or known to be positive for HCV ribonucleic acid (RNA) or HBsAg (HBV surface antigen)
* Known human immunodeficiency virus (HIV) infection
* Any medical condition which, in the investigator's opinion, could compromise the patient's safety
* Patients unable to swallow tablets or patients with malabsorption syndrome, or any other disease significantly affecting gastrointestinal function
Healthy Volunteers:
False
Sex:
ALL
Study:
NCT02485535
Study Brief:
Protocol Section:
NCT02485535