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 @ 11:50 AM
Ignite Modification Date:
2025-12-24 @ 11:50 AM
NCT ID:
NCT02499861
Eligibility Criteria:
Inclusion Criteria:
* Age ≥ 2 years of age and \< 21 years of age at time of study enrollment
* Able to swallow genistein or take it with a puree.
* Patients must have a diagnosis of recurrent or refractory solid tumors, including Central Nervous System tumors, lymphoma or leukemia for which standard curative measures do not exist or are no longer effective
* For solid tumors, patients must have either measurable or evaluable disease. For leukemia, patients must have \> 5% blasts in the bone marrow.
* Patients must have fully recovered from the acute toxic effects of all prior anti-cancer therapy.
* Performance level: Karnofsky ≥50% for patients ≥ 16 years of age or Lansky ≥ 50% for patients \< 16 years of age
* Life expectancy at least one month
* Patients must have adequate bone-marrow function
* Patients must have normal organ as defined below: (total bilirubin ≤ 24microM/L), Amylase/pancreatic amylase≤1.5 × institutional upper limit of normal, Aspartate Aminotransferase (AST) /Alanine Aminotransferase (ALT) ≤2.5 × institutional upper limit of normal, creatinine clearance ≥60 mL/min/1.73 m2.
OR creatinine according to age/gender
* Nervous system disorders (CTCAE v4) resulting from prior therapy must be ≤ Grade 2
* Participants of child-bearing potential and men must agree to use adequate contraception for the duration of study treatment, and 4 months after completion of decitabine and genistein administration.
* All patients and/or their parents or legally authorized representatives must sign a written informed consent
Exclusion Criteria:
* Prior decitabine or genistein therapy.
* Patients who are receiving any other investigational agents.
* Nasogastric or gastrostomy (or equivalent) administration of genistein is not allowed.
* Patients with known exclusive non-measurable leptomeningeal disease at enrolment should be excluded from this clinical trial.
* History of allergic reactions attributed to compounds of similar chemical or biologic composition to decitabine and genistein.
* Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection (receiving antibiotics), symptomatic heart or lung disease, or psychiatric illness/social situations that would limit compliance with study requirements.
* Pregnant or breast-feeding women are excluded from this study. All girls of child bearing potential must have a negative pregnant test prior to enrolment.
* Patients who in the opinion of the investigator may not be able to comply with the safety monitoring requirements of the study are not eligible.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
2 Years
Maximum Age:
20 Years
Study:
NCT02499861
Study Brief:
Protocol Section:
NCT02499861