CELL INTELLIGENCE · 肿瘤细胞治疗研究

Inclusion Criteria:

1. 18 to 70 years old, male or female;
2. Newly diagnosed as high-risk multiple myeloma:

   * Revised Multiple Myeloma International Staging System (R-ISS) stage 3;
   * Double-hit or triple-hit according to FISH test.
3. Presence of measurable lesions during screening according to any of the following criteria:

   * The proportion of primitive naive or monoclonal plasma cells ≥ 5% by bone marrow cytology, bone marrow biopsy histology or flow cytometry;
   * Serum monoclonal protein (M-protein) level: M protein ≥10 g/L for IgG type, M protein ≥5g/L for IgA, IgD, IgM, and IgE type;
   * Urine M protein level ≥200 mg/24 hours;
   * Light chain multiple myeloma without measurable lesions in serum or urine: the affected serum free light chain ≥100 mg/L with abnormal serum κ/λ free light chain ratio;
4. ECOG score of 0 or 1;
5. Expected survival time ≥ 12 weeks;
6. Subjects must have appropriate organ functions and meet all the following laboratory test requirements before enrollment:

   * Hematology: Absolute neutrophil count (ANC) ≥ 1×10\^9/L (prior growth factor support is allowed, but supportive treatment within 7 days before laboratory test is not allowed); Absolute lymphocyte count (ALC) )≥0.3×10\^9/L; platelets≥75×10\^9/L (blood transfusion support within 7 days before laboratory test is not allowed); hemoglobin ≥60 g/L (without red blood cell \[RBC\] transfusion within 7 days before laboratory test; recombinant human erythropoietin is allowed);
   * Liver function: Alanine aminotransferase (ALT) and aspartate aminotransferase (AST)≤2.5×upper limit of normal (ULN); serum total bilirubin≤1.5×ULN;
   * Renal function: creatinine clearance calculated according to Cockcroft-Gault formula≥ 40 ml/min.
   * Coagulation function: fibrinogen ≥1.0 g/L; activated partial thromboplastin time≤1.5×ULN, prothrombin time (PT)≤1.5×ULN;
   * Blood oxygen saturation\>91%;
   * Left ventricular ejection fraction (LVEF) ≥50%;
7. Subjects and their spouses agree to take effective tools or contraceptive measures (safe period contraception is not included) from the time the subject signs the informed consent form until one year after the CAR-T cell infusion.

Exclusion Criteria:

1. Patient who needs chronic use of immunosuppressive agents;
2. Patient with hypertension that cannot be controlled by medication;
3. Severe heart disease: including but not limited to unstable angina, myocardial infarction (within 6 months before screening), congestive heart failure (New York Heart Association \[NYHA\] classification ≥ grade III), severe arrhythmia;
4. Unstable systemic diseases judged by the investigator: including but not limited to severe liver, kidney or metabolic diseases that require drug treatment;
5. Patients with malignant tumors other than multiple myeloma within 5 years before screening, excluding fully treated cervical carcinoma in situ, basal cell or squamous cell skin cancer, local prostate cancer after radical resection, and those after radical resection Ductal carcinoma in situ of breast;
6. Patient with a history of solid organ transplantation;
7. Patient who is suspected with or with symptoms of central nervous system invasion by plasma cell tumors;
8. Multiple myeloma patients with plasma cell leukemia;
9. Positive hepatitis B surface antigen (HBsAg) or hepatitis B core antibody (HBcAb) and detectable hepatitis B virus (HBV) DNA in peripheral blood; hepatitis C virus (HCV) antibody positive and peripheral blood hepatitis C virus ( HCV) RNA positive; human immunodeficiency virus (HIV) antibody positive; cytomegalovirus (CMV) DNA test positive; syphilis test positive;
10. Women who are pregnant or breastfeeding;
11. Patient with mental illness or disturbance of consciousness or central nervous system disease;
12. Major surgery history within 2 weeks before entering the study, or scheduled surgery during the study period or within 2 weeks after the study treatment;
13. Other situations considered unsuitable by the investigator.

主要终点：Proportion of Minimal Residual Disease (MRD)-negative subjects · The proportion of subjects who achieve MRD-negativity after CT103A infusion. · Up to 2 years after CT103A infusion；Median progression-free survival (mPFS) · The median time from the date of CT103A infusion to the date of first disease progression or death from any cause. · Up to 2 years after CT103A infusion
次要终点：Best overall response (BOR)；Median survival (mOS)；Event-free survival (EFS)；Duration of response (DOR)；Safety endpoint；Pharmacokinetic(PK) endpoint；PK endpoint - Tmax；PK endpoint - AUC 0 to 28d and AUC 0 to 90d

• CT103A in Newly Diagnosed Subjects With High-risk Multiple Myeloma · EXPERIMENTAL · Fully Human BCMA Chimeric Antigen Receptor Autologous T Cell Injection（CT103A）will be infused at 1.0 x 10\^6 CAR+ T cells/kg in newly diagnosed subjects with high-risk multiple myeloma

This study is a multi-center, single-arm clinical study to evaluate the efficacy, safety, pharmacokinetics and pharmacodynamic characteristics of CT103A as the first-line treatment in newly diagnosed high-risk multiple myeloma subjects with induction chemotherapy as bridging therapy.