Phase 1/2 Study of CD19 Chimeric Antigen Receptor T-cell (CD19 CAR-T; PL001) for Relapsed or Refractory B-cell Lymphoma

Prior treatment

• Prior CD19 targeted therapy, such as CAR-T, Bi-specific T-cell engagers (BiTE), or monoclonal antibody.
• History of autologous HSCT within 3 months prior to consent.
• Received any investigational product within 4 weeks prior to consent.
• Systemic anticancer therapy within 3 weeks prior to apheresis.
• Long-term use of systemic corticosteroids, defined as daily use \>10 mg of prednisolone or equivalent, within 2 weeks prior to leukapheresis.
  • Exception examples:
  • Nasal, ophthalmic, inhaled, intra-articular, and topical steroid preparation.
  • Short term systemic steroid for drug, contrast, or blood transfusion allergic reaction management.
  • Low dose maintenance steroid therapy for other conditions (e.g., asthma).
• Use of long-acting and short-acting myeloid growth factor within 2 weeks, 5 days prior to leukapheresis, respectively.
• Received anti-thymocyte globulin within 4 weeks prior to consent.
• Intrathecal chemotherapy within 1 week prior to leukapheresis.
• Uncontrolled acute life-threatening bacterial, viral, or fungal infection (e.g., the need for intravenous therapeutic antibiotics, blood culture positive ≤72 hours prior to apheresis).
  • 21\. Any medical conditions which might compromise the patient's safety from leukapheresis, lymphodepletion chemotherapy, or CAR-T therapy and anticipated AEs, according to the Investigator's evaluation.
  • 22.Patients with insufficient leukapheresis cells.
  • Screening 2:
• Use of long-acting and short-acting myeloid growth factor within 12 days, 2 days prior to lymphodepletion therapy, respectively.
• Uncontrolled acute life-threatening bacterial, viral, or fungal infection (e.g. the need for intravenous therapeutic antibiotics, blood culture positive ≤72 hours prior to lymphodepletion).

Other illness

• History of cancers (includes myelodysplastic syndrome) other than non-melanoma skin cancer or carcinoma in situ (e.g., cervix, bladder, breast) unless disease-free without active treatment for at least 3 years.
• History of allogeneic HSCT.
• Active hepatitis B virus (HBV) infection defined as detectable HBV DNA (Patients with positive anti-hepatitis B core antibody \[HBcAb\] must consent to regular monitoring of HBV DNA, and anti-HBV prophylaxis with oral anti-viral agent (such as entecavir) is mandatory until End-of-Study visit \[Visit 15\].)
• Active hepatitis C virus (HCV) infection defined as positive anti- HCV antibody plus detectable HCV RNA.
• Positive for human immunodeficiency virus (HIV) or human T-cell lymphotropic virus (HTLV) infection.
• Long-term use of systemic corticosteroids, defined as daily use \>10 mg of prednisolone or equivalent.
  • Exception examples:
  • Nasal, ophthalmic, inhaled, intra-articular, and topical steroid preparation.
  • Short term systemic steroid for drug, contrast, or blood transfusion allergic reaction management.
  • Low dose maintenance steroid therapy for other conditions (e.g., asthma).
• Any medical condition which might compromise the patient's safety because of lymphodepletion chemotherapy or CAR-T therapy and anticipated AEs, according to the Investigator's opinion.

Lab values

• Inadequate major organ functions at Screening, which were defined as any of below:
  • absolute neutrophil count (ANC) \<500/µL
  • Absolute lymphocyte count (ALC) \<300/µL, excluding leukemic cells.
  • Hemoglobin (Hb) \<8.0 g/dL
  • Platelet count \<75,000/µL without transfusion support within 3 days
  • e. Baseline O2 saturation \<92% by pulse oximetry at room air
  • Significant CNS diseases such as dementia, major stroke, seizure while under antiepileptic drug
  • Aspartate aminotransferase (AST) \>5 × upper limit of normal (ULN) and alanine aminotransferase (ALT) \>5 × ULN, or total bilirubin \>2 × ULN (except for constitutional jaundice)
  • Serum creatinine \> 1.5 × ULN and estimated glomerular filtration rate (eGFR) \< 60 mL/min/1.73 m², as calculated by the Cockcroft-Gault formula.
  • Significant cardiac disease including but not limited to: left ventricular ejection fraction (LVEF) \<50%, QTc(the corrected QT interval) \> 480 msec based on Fredericia's formula, clinically significant arrhythmias, history of myocardial infarction or unstable angina within 3 months prior to consent.
• Inadequate major organ functions at Screening which were defined as any of below:
  • ANC \<500/µL
  • Hb \<8.0 g/dL
  • Platelet count \<50,000/µL, without transfusion support within 3 days
  • Baseline O2 saturation \<92% by pulse oximetry on room air
  • AST \>5 × ULN and ALT\>5 × ULN, or total bilirubin \>2 × ULN (except for constitutional jaundice)
  • Significant CNS diseases such as dementia, major stroke, seizure while under antiepileptic drug
  • Serum creatinine \> 1.5 × ULN and estimated glomerular filtration rate (eGFR) \< 60 mL/min/1.73 m², as calculated by the Cockcroft-Gault formula.

Other

• Screening 1:
• Chronic lymphocytic leukemia with Richter's transformation.
• Primary CNS lymphoma. (Non-primary CNS lymphoma with CNS involvement is eligible).
• Primary intra-ocular lymphoma.

• Screening 1:
• Patient is ≥14 years of age, inclusive, at the time of signing the informed consent.
• Histologically confirmed diagnosis of diffuse large B-cell lymphoma (DLBCL), primary mediastinal large B-cell lymphoma (PMLBCL), large B-cell lymphoma transformed from follicular lymphoma (FL), or grade 3a or 3b FL.
• On-site documentation of CD19 on the dominant population of cancer cells.
• Disease status should meet any one of the below:
  • Patients with previous autologous-hematopoietic stem cell transplantation (auto HSCT) have relapsed, progressive, or refractory disease (defined as having not achieved a CR) after transplantation regardless of lines of systemic therapy.
  • Patients without previous HSCT have relapsed, progressive, or refractory disease (defined as having not achieved a CR) after at least 2 lines of systemic therapy, including anti-CD20 antibody and anthracycline.
• Have no available effective systemic therapy as judged by the Investigator.
• At least one measurable non-CNS (central nervous system) lesion based on Lugano classification for lymphoma.
• Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2.
• Life expectancy of at least 3 months.
• Patient is male or female.
• A male patient must agree to use a highly effective contraception as detailed in Section 10.4 (Appendix 4) during the treatment period and for at least 2 years after the dose of PL001 and refrain from donating sperm during this period.
  • Female Patients:
• A female patient is eligible to participate if she is not pregnant (Section 10.4; Appendix 4), not breastfeeding, and at least one of the following conditions applies:
  • Not a woman of childbearing potential (WOCBP) as defined in Section 10.4 (Appendix 4).
  • OR
  • A WOCBP who agrees to follow the contraceptive guidance in Section 10.4 (Appendix 4) during the treatment period and for at least 2 years after the dose of PL001 and refrain from donating ova during this period.
• Patient/patient's parent/legal guardian is capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in this protocol.
  • Screening 2:
• Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2.
• CAR-T is successfully manufactured and ready for use, from cells harvested by non mobilized leukapheresis.
• WOCBP who have a negative serum pregnancy test at Screening 2.