A Clinical Study of ONCT-808 in Subjects With Relapsed or Refractory B-Cell Malignancies

This is an interventional treatment trial for Relapsed/Refractory Aggressive B-Cell Malignancies focused on measuring Lymphoma, Lymphoma, B-Cell, Lymphoma, Large B-Cell, Diffuse, Lymphoma, Mantle Cell, Lymphoproliferative Disorders, Lymphatic Diseases, Immunoproliferative Disorders, Immune System Diseases, Lymphoma, Non-Hodgkin, ROR1, CAR-T cell therapy, Autologous CAR-T cell therapy, Adoptive cellular therapy, Cellular immunotherapy Read More

Key Inclusion Criteria:

• Over 18 years old

• Histologically confirmed aggressive B-cell NHL, including:

  • MCL, with diagnosis confirmed by cyclin D1 overexpression or evidence of t (11;14) translocation

  • LBCL, including:

    • DLBCL NOS
    • Primary mediastinal LBCL
    • High-grade BCL
    • DLBCL arising from follicular lymphoma
    • Follicular lymphoma grade 3B
    • Richter's syndrome
• Availability of archival tissue for immunohistology, or willing to undergo baseline biopsy if not available

• R/R with no available therapy. Subject must have:

  • Received prior systemic therapy that has included an alkylating agent, anthracycline, and an anti-CD20 mAb
  • Received and progressed after autologous hematopoietic stem cell transplant (HSCT) or is ineligible for or has refused to receive HSCT
  • Received prior approved CD19 CAR T-cell therapy or is ineligible for or has refused CD19 CAR-T

• Minimum washout period between previous systemic therapy and leukapheresis includes:

  • Chemotherapy: at least 14 days or 5 half-lives, whichever is shorter
  • Autologous HSCT: at least 3 months
  • CD19 CAR T-cell therapy: at least 6 months
• ≥1 measurable lesion per Lugano criteria (Cheson, 2014)
• Subject has Fluorodeoxyglucose (FDG)-avid disease.
• Subject has an ECOG performance status of 0 or 1.

• Subject has adequate organ function:

  • ALC ≥100/uL
  • ANC ≥1000/uL (≥500/uL if due to lymphoma; growth factors allowed)
  • Hgb ≥8 g/dL (transfusion allowed)
  • Platelets ≥75,000/uL (≥50,000/uL if due to lymphoma; transfusion allowed)
  • CrCL ≥50 ml/min; AST/ALT ≤2.5x ULN, T. bili ≤1.5 mg/dl (except Gilbert's)
  • EF ≥50% by ECHO/MUGA; NCS ECG, NCS pleural effusion; O2 sat >92%
• Subject has an estimated life expectancy of >12 weeks

Key Exclusion Criteria:

• Prior ROR1-targeted therapy
• Current or anticipated systemic immunosuppressive therapy (e.g., prednisone >5 mg) from LD chemo until Day 28 post ONCT-808 dosing
• If receiving anticoagulation therapy, subject is unable to hold therapy for 3 days prior and 28 days following ONCT-808 administration
• Known CNS involvement by malignancy within 6 months
• H/o or current CNS disorder (e.g., seizure, CVA, dementia, cerebellar disease, cerebral edema, posterior reversible encephalopathy syndrome or any autoimmune disease with CNS involvement) within 6 months of study entry
• Clinically significant cardiovascular disease (e.g., MI, UA, CABG, or CHF grade ≥2 NYHA within 12 months of planned ONCT-808 dosing) or serious arrhythmia requiring medication
• Evidence of HIV infection or active HBV, HCV
• Systemic fungal infection requiring medication in the last 12 months
• H/o Covid-19 infection with residual lung infiltrate/fibrosis
• H/o other malignancy except non-melanoma skin cancer or carcinoma in situ not in remission for ≥2 years
• H/o autoimmune disease resulting in end organ injury or require systemic immunosuppression within last 2 years
• H/o allogeneic HSCT or organ transplant