About this trial
The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics, and efficacy of ponatinib in children aged 1 to \< 18 years with advanced leukemias, lymphomas, and solid tumors.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Karnofsky performance status ≥ 40% for participants ≥ 16 years old or Lansky Play Scale ≥ 40% for pediatric participants < 16 years old.
Participants must have recovered to < Grade 2 per the NCI CTCAE v5.0 or to baseline from any non-hematologic toxicities (except alopecia) due to previous therapy.
Willingness to avoid pregnancy or fathering children.
Immunosuppressive therapy (including post stem cell transplant regimens) within 14 days before the first dose of ponatinib.
Disqualifiers
None
Trial design
Single group
Treatments tested in this trial
Ponatinib
DrugPonatinib administered as a tablet or age-appropriate formulation for pediatric participants according to age-based cohort assignment.
Treatment groups
Trial outcomes
Primary outcomes
Phase 1: Number of dose-limiting toxicities
Defined as the occurrence of any protocol-defined toxicities occurring after dosing and up to and including Day 28, except those toxicities with a clear alternative explanation.
Phase 2: Efficacy of ponatinib assessed by major cytogenetic response (MCyR) in participants with chronic-phase chronic myeloid leukemia (CP-CML)
Defined as complete cytogenetic response (CCyR) or partial cytogenetic response (PCyR) as assessed by conventional cytogenetics or fluorescence in situ hybridization (FISH).
Phase 2: Efficacy of ponatinib assessed by major hematologic response (MaHR) or major molecular response (MMR) in participants with BCR-ABL-positive leukemias
Assessed by polymerase chain reaction (PCR).
Phase 2: Efficacy of ponatinib assessed by complete response (CR) in participants with leukemias other than BCR-ABL-positive leukemias to determine the efficacy of ponatinib
Secondary outcomes
Phase 1: Number of treatment-emergent adverse events
Phase 1: Tmax of ponatinib
Time to maximum concentration.
Phase 1: AUCss,0-24 of ponatinib
Area under the steady-state plasma or serum concentration-time curve from Hour 0 to 24.
Phase 1: t½ of ponatinib
Apparent terminal-phase disposition half-life.
Sponsors and contacts
Click on the lead sponsor to view all of their trials.