ALL, Adult B Cell, ALL, Childhood, B-cell Leukemia, B-cell Lymphoma, CLL/SLL, DLBCL - Diffuse Large B Cell Lymphoma, NHL, Relapsed, Adult
Conditions
Brief summary
This study is a multi-center study to evaluate the safety of KUR-502 in subjects with refractory/relapsed B-cell NHL or leukemia (ALL or CLL).
Detailed description
KUR-502 will be manufactured from leukapheresis products from healthy donors. Subjects will be enrolled into 2 parallel cohorts (Cohort A \[non-ALL\] and Cohort B \[ALL\]). Each cohort will undergo dose escalation independently. Three (3) dose levels will be evaluated in the ANCHOR and ANCHOR2 studies combined (1×107/m2, 3×107/m2, 1×108/m2). Dose levels are defined based on the number of transduced KUR-502 cells. Body surface area (BSA) will be capped at 2.4 m2. Subjects will receive \<1×104 allogeneic T cells/kg at any dose level. The MTD will be determined once dose escalation is completed, and all subjects are evaluable for DLT. If there is no DLT that determines an MTD, a maximum dose level will be declared. Dose escalation will stop when 6 subjects have been treated at the MTD or highest dose level.
Interventions
GENETICKUR-502
KUR-502 (CD19.CAR-aNKT cells) consists of transduced allogeneic natural killer T cells (aNKT) genetically modified with additional features to enhance their anti-tumor activity against CD19+ B-cell malignancies. Following intravenous (IV) infusion, the product is expected to kill CD19+ tumor cells by direct interaction with the chimeric antigen receptor (CAR), and activation of the NKT cells to kill tumor through their innate cell killing.
Sponsors
Athenex, Inc.
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
Phase 1 dose escalation
Eligibility
Sex/Gender
ALL
Age
3 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
Subjects must meet all of the following criteria to be included in this study: 1. Signed written informed consent. 2. Diagnosis of CD19+ B-cell lymphoma or leukemia (ALL or CLL). * Subjects who previously received CD19-directed therapy must have biopsy or flow cytometry-confirmed CD19+ tumor following the CD19-directed therapy; may be performed by local laboratory. 3. The disease is: Cohort A (non-ALL subjects): * Relapsed or refractory after ≥2 lines of therapy, including a CD20 antibody, if an indolent lymphoma. * Relapsed or refractory after ≥2 lines of therapy, including ibrutinib and venetoclax, if CLL. * Relapsed or refractory after ≥2 lines of therapy, including a CD20 antibody and an anthracycline, and the subject is ineligible for autologous stem cell transplantation, if an aggressive or highly aggressive lymphoma. * Ineligibility for autologous stem cell transplantation includes non-responsive disease after salvage therapy and failure to mobilize stem cells for transplant. Cohort B (ALL subjects): * Relapsed or refractory after ≥2 lines of therapy. 4. Measurable disease by current criteria (Lugano criteria for lymphomas, IWG criteria for CLL, and detectable disease for ALL). 5. Age 3 to 75 years; subjects \<18 years old will not be enrolled as the first subject on any dose level. 6. BSA ≤2.4 m2. 7. Bilirubin \<2 times the upper limit of normal (ULN) (3 times if the subject has Gilbert syndrome). 8. Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) \<5 times ULN. 9. Estimated glomerular filtration rate (GFR) ≥50 mL/min. 10. Pulse oximetry ≥90% on room air. 11. Karnofsky or Lansky score ≥70. 12. Recovered from the acute toxic effects of all prior chemotherapy based on the enrolling physician's assessment (if some effects of chemotherapy are expected to last long term, for example, residual neuropathy, anemia, or alopecia, subject is eligible if meets other eligibility criteria). 13. Life expectancy \>12 weeks.
Exclusion criteria
Subjects who meet any of the following criteria will be excluded from this study: 1. Females who are breastfeeding or pregnant at Screening (as documented by a positive urine or serum pregnancy test; may be performed by local laboratory). 2. Females of childbearing potential who: * Had unprotected sexual intercourse within 30 days before study entry and who do not agree to use a highly effective method of contraception (eg, total abstinence, an intrauterine device, a double-barrier method \[such as condom plus diaphragm with spermicide\], a contraceptive implant, an oral contraceptive, or have a vasectomized partner with confirmed azoospermia) through the Day 365 visit or for 30 days after study drug discontinuation. * Are currently abstinent, and do not agree to use a double-barrier method (as described above) or refrain from sexual activity through the Day 365 visit or for 30 days after study drug discontinuation. * Are using hormonal contraceptives but are not on a stable dose of the same hormonal contraceptive product for at least 4 weeks before dosing and who do not agree to use the same contraceptive through the Day 365 visit or for 30 days after study drug discontinuation. 3. Males who have not had a successful vasectomy (confirmed azoospermia) or they and their female partners do not meet the criteria above (ie, not of childbearing potential or practicing highly effective contraception through the Day 365 visit or for 30 days after study drug discontinuation). No sperm donation is allowed through the Day 365 visit or for 30 days after study drug discontinuation. 4. Currently receiving any investigational agents or received any cellular therapies within the previous 6 weeks prior to the KUR-502 infusion. 5. History of Grade 2 to 4 GvHD. 6. History of hypersensitivity reactions to murine protein-containing products. 7. Active infection with human immunodeficiency virus (HIV) or human T cell lymphotropic virus (HTLV). 8. Active infection with hepatitis B virus (HBV) or hepatitis C virus (HCV). 9. Uncontrolled active bacterial, fungal, or other viral infection.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Dose limiting toxicity (DLT) rate and grade of single dose of Kur-502 | 4 weeks post T cell infusion | Incidence rate and the grade (severity) of dose-limiting toxicities (DLTs) based on adverse events (AEs) reported according to the National Cancer Institute (NCI) - Common Terminology Criteria for Adverse Events (CTCAE) v5.0 |
Countries
United States
Contacts
Primary ContactDan Lang, MD, PhD
Outcome results
None listed