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 @ 4:49 PM
Ignite Modification Date:
2025-12-24 @ 4:49 PM
NCT ID:
NCT02518750
Eligibility Criteria:
Inclusion Criteria:
* Participants must have relapsed or refractory acute lymphoblastic leukemia or lymphoma (ALL):
* Stratum I: T-cell lymphoblastic leukemia or lymphoma in first relapse or refractory to one or two courses of frontline induction therapy.
* Stratum II: B-cell or T-cell lymphoblastic leukemia or lymphoma in second or third relapse or refractory to 2 or 3 induction or re-induction attempts. Patients with Ph+ ALL must be refractory or relapsed after treatment with regimen that included a tyrosine kinase inhibitor (TKI).
* Relapse in ALL is defined as the reappearance (in a patient who has previously achieved remission) of leukemic blasts in the bone marrow.
* Should flow cytometric analyses suggest relapse (by the reappearance of a similar immunophenotype to the original leukemia) in the presence of \<5% blasts morphologically, a repeat bone marrow test is recommended to confirm relapse.
* Molecular or genetic relapse is characterized by the reappearance of a cytogenetic or molecular abnormality.
* Age is ≤ 21 years (participant has not yet reached 22nd birthday).
* Able to swallow capsules.
* Karnofsky or Lansky performance score is ≥ 60%. The Lansky performance score should be used for participants \< 16 years and the Karnofsky performance score for participants ≥ 16 years.
* Prior therapy:
* There is no waiting period for participants who relapse while receiving therapy if they are free from side effects attributable to such therapy.
* Emergent radiation therapy, one dose of intrathecal chemotherapy and up to 7 days of steroids or hydroxyurea are permitted before start of treatment in participants who relapse after completion of frontline therapy. Other circumstances must be cleared by PI or medical designee.
* At least 90 days have elapsed since bone marrow transplant and participant is off immune suppression for ≥ 2 weeks, if applicable.
* Adequate renal function defined as glomerular filtration rate ≥ 60 cc/min/1.73m\^2 or serum creatinine based on age as follows:
* If age is 1 to 2 years, then maximum serum creatinine (mg/dL) is 0.6 for males or females.
* If age is 2 to 6 years, then maximum serum creatinine (mg/dL) is 0.8 for males or females.
* If age is 6 to 10 years, then maximum serum creatinine (mg/dL) is 1 for males or females.
* If age is 10 to \<13 years, then maximum serum creatinine (mg/dL) is 1.2 for males or females.
* If age is 13 to 16 years, then maximum serum creatinine (mg/dl) is 1.5 for males or 1.4 for females.
* If age is \> 16 years, then maximum serum creatinine (mg/dl) is 1.7 for males or 1.4 for females.
* Adequate hepatic function defined as:
* Direct bilirubin ≤ 1.4 mg/dL (if total bilirubin \> 1.4 mg/dL) AND
* AST and ALT \< 5 x ULN for age.
* Adequate cardiac function defined as shortening fraction of ≥ 27% or ejection fraction ≥ 45%.
* Lymphoma participants without bone marrow involvement must have:
* Absolute neutrophil count (ANC) \>1,000/mm3, AND
* Platelet count ≥50,000/mm\^3 (without transfusion support)
* NOTE: These criteria are waived for participants with leukemia or lymphoma participants with bone marrow involvement.
* Written, informed consent and assent following Institutional Review Board, NCI, FDA and OHRP guidelines.
Exclusion Criteria:
* Prior histone deacytylases (HDAC), DAC, HSP90 inhibitors or valproic acid for treatment of cancer.
* Patients who will need valproic acid for any medical condition during the study or within 5 days prior to first panobinostat treatment.
* Impaired cardiac function or clinically significant cardiac diseases, history of arrhythmia (including ventricular fibrillation or torsade de pointes), bradycardia \<50 bpm, screening ECG with prolonged QTc or uncontrolled hypertension.
* Impairment of gastrointestinal (GI) function or GI disease that may significantly alter the absorption of panobinostat.
* Patients with diarrhea \> CTCAE grade 2.
* Other concurrent severe and/or uncontrolled medical conditions (e.g., uncontrolled diabetes or active or uncontrolled infection) including abnormal laboratory values, that could cause unacceptable safety risks or compromise compliance with the protocol.
* Patients using medications that have a relative risk of prolonging the QT interval or inducing torsade de pointes if treatment cannot be discontinued or switched to a different medication prior to starting treatment.
* Patients who have received targeted agents within 2 weeks or within 5 half-lives of the agent and active metabolites (whichever is longer) and who have not recovered from side effects of those therapies.
* Patients who have undergone major surgery ≤ 4 weeks prior to starting treatment or who have not recovered from side effects of such therapy.
* Patients with known positivity for human immunodeficiency virus (HIV) or hepatitis B/C.
* Inability to swallow capsules.
* Active, uncontrolled infection or severe concurrent medical disease, including but not limited to congestive heart failure, cardiac arrhythmias, or psychiatric illness.
* Isolated extramedullary relapse (leukemia) or isolated CNS lymphoma.
* Pregnant or lactating (female participant of childbearing potential must have negative serum or urine pregnancy test required within 7 days prior to start of treatment). Male or female of reproductive potential has agreed to use effective contraception method for duration of study treatment.
* Down syndrome.
* Inability or unwillingness or research participant or legal guardian/representative to give written informed consent.
Healthy Volunteers:
False
Sex:
ALL
Maximum Age:
21 Years
Study:
NCT02518750
Study Brief:
Protocol Section:
NCT02518750