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Active, not recruiting Phase 1

Safety/PK Study of Gene Modified Donor T Cell Infusion in Children With Recurrent Hem Malignancies After Allo Transplant

NCT03459170 · tracked via the Priya Life Science Italy tracker
Phase
Phase 1
Started
2018-02-01
Last updated
2022-07-12

Condition(s) studied

Hematologic Malignancy

Investigational drug(s) / intervention(s)

BPX-501 T cells →rimiducid →

BPX-501 T cells: Biological: T cells transduced with CaspaCIDe® safety switch

rimiducid: administered to eliminate BPX-501 cells in the event of GVHD

Study summary

Phase I, open-label, non-randomized study of safety, pharmacokinetics and efficacy of donor BPX-501 T cell infusion in children with recurrent or minimal residual disease (MRD) hematologic malignancies post-allogeneic transplant. The study will consist of the Main Study and an optional Pharmacokinetics (PK) Sub-Study.

Eligibility

Sex
ALL
Min age
1 Year
Max age
18 Years
Healthy volunteers
No
Inclusion Criteria: * Patients aged \< 18 * Clinical diagnosis of one of the following pediatric hematological malignancies: * High-risk Acute Leukemia (Acute lymphoblastic leukemia \[ALL\] or acute myeloid leukemia \[AML\]) in any CR * Acute Leukemia that is minimal residual disease (MRD) positive at \> 1copy per 1 x 10,000 reference copies pre-HSCT * Myelodysplastic Syndrome (MDS) * Hodgkin or Non-Hodgkin lymphomas * Other high-risk hematological malignancy in CR eligible for stem cell transplantation per institutional standard * Patients with a hematological malignancy who have received a prior allogeneic HSCT * Patients with on-treatment relapse of AML within 6 months of initial CR * Patients relapsing within 6 months of initial diagnosis of hematological malignancy. * Planned or previous treatment of hematological malignancy with one of the following: * Matched related HSCT * Mismatched related HSCT * For patients who have received a transplant, occurrence of one of the following \> 30 days post-HSCT: * Minimal residual disease (MRD) positive at \> 1 copy per 1 x 10,000 reference copies post-HSCT * Decreasing donor chimerism detected on two bone marrow biopsies or peripheral blood analyses at a \> 7-day interval * Recurrent disease * Life expectancy \>10 weeks; * Signed donor and patient/guardian informed consent; * For mismatched related donor recipients, a minimum genotypic identical match of 5/10 is required, as determined by high resolution typing, at least one allele of each of the following genetic loci must be matched: HLA-A, HLA-B, HLA-C, HLA- DRB1, and HLA-DQB1. * Performance status: Karnofsky/Lansky score \> 70%. * Adequate organ function as measured by: * High-risk Acute Leukemia (Acute lymphoblastic leukemia \[ALL\] or acute myeloid leukemia \[AML\]) in any CR * High-risk Acute Leukemia (Acute lymphoblastic leukemia \[ALL\] or acute myeloid leukemia \[AML\]) in any CR * Hepatic: direct bilirubin ≤ 3x ULN, or AST/ALT ≤ 5x ULN. * Bone marrow; * \> 25% donor T cell chimerism * ANC \>1 x 10\^9/L. * Cardiac: LVEF at rest \>45%. * Pulmonary: FEV 1, FVC, DLCO (diffusion capacity for CO) \> 50% predicted (corrected for hemoglobin); for children who are unable to perform pulmonary function tests due to age or developmental ability, there must be no evidence of dyspnea or no need for supplemental oxygen as evidenced by 02 saturation ≥ 92% on room air. * Hepatic: direct bilirubin ≤ 3x ULN, or AST/ALT ≤ 5x ULN. * Renal: creatinine clearance ≤ 2x of ULN for age Exclusion Criteria: ≥ Grade II acute GVHD or moderate to severe chronic GVHD due to a previous allograft at the time of screening; * Active CNS involvement by malignant cells (\< 2 months prior to time of consent); * Current uncontrolled bacterial, viral or fungal infection (currently taking medication with evidence of progression of clinical symptoms or radiologic findings). * Positive HIV serology or viral RNA; * Pregnancy (positive serum βHCG test) or breast-feeding female; * Patients of reproductive age unwilling to use effective forms of birth control or abstinence for a year after BPX-501 T cell infusion.

Primary outcome measure(s)

  • BPX-501 Safety — Month 24
    Incidence of treatment emergent adverse events of 2 stratified dose levels of BPX-501 T cell infusions based on patient-donor match in pediatric subjects with hematologic malignancies
  • Mean plasma concentration — pre-dose, 30 min, 2 hours and 8 hours after start of infusion
    Measure plasma concentrations of rimiducid (AP1903) at two doses (Arm 1: 0.04mg/kg; Arm 2: 0.4mg/kg) in pediatric subjects, during and after a 2-hour infusion

Trial sites (3)

FacilityCityRegionStatus
San Matteo Hospital Pavia Italy
IRCCS Ospedale Pediatrico Bambino Gesù Rome Italy
Ospedale Infantile Regina Margherita Turin Italy
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03459170 on ClinicalTrials.gov ↗ ← All trials in Italy