A Clinical Study to Evaluate the Safety and Preliminary Efficacy of QI-019B in Patients With Relapsed/Refractory Multiple Myeloma.

Prior treatment

• 1.During screening, participants who have received other anticancer treatments (based mainly on investigator judgment):
  • Received targeted therapy, epigenetic therapy, other investigational drugs, or treatment using invasive research medical devices within 5 half-lives;
  • Received immune/non-immune-directed systemic therapy within 1 week;
  • Received cytotoxic therapy within 2 weeks;
  • Received proteasome inhibitors within 2 weeks;
  • Received immunomodulatory therapy within 1 week.
  • Received radiotherapy within 4 weeks (if the radiotherapy covered ≤5% of bone marrow reserve, the subject is eligible regardless of the radiotherapy end date);
• 2\. Received allogeneic hematopoietic stem cell transplantation within 6 months or autologous hematopoietic stem cell transplantation within 3 months before infusion;
• 3\. Had malignancies other than MM before screening, except for: malignancies treated with curative intent, with no known active disease ≥2 years prior to enrollment; or adequately treated non-melanoma skin cancer with no evidence of disease currently;
• 4\. Received any treatment using vesicular stomatitis virus G (VSVG) pseudotyped virus;
• 6\. Within 6 months before infusion, tested positive for hepatitis B surface antigen (HBsAg) or hepatitis B core antibody (HBcAb) with peripheral blood HBV DNA levels above the normal range; tested positive for hepatitis C virus (HCV) antibody with peripheral blood HCV RNA levels above the normal range; tested positive for human immunodeficiency virus (HIV) antibody; or tested positive for syphilis;
• 7\. Had symptomatic heart failure or other serious cardiac diseases such as severe arrhythmias:
  • New York Heart Association (NYHA) class III or IV congestive heart failure;
  • Experienced myocardial infarction or underwent coronary artery bypass graft (CABG) or coronary stent implantation within 6 months prior to signing the ICF;
  • Had clinically significant ventricular arrhythmias, or a history of unexplained syncope (excluding cases caused by vasovagal response or dehydration);
  • Had a history of severe non-ischemic cardiomyopathy;
• 8\. Other clinically significant diseases, including:
  • Primary immunodeficiency;
  • Stroke or seizure within 6 months prior to screening;
  • Clear clinical evidence of dementia or altered mental status;
  • Parkinson's disease or Parkinsonian movement disorders or history thereof;
• 9\. Undergoing surgery within 2 weeks of administration or planned surgery within 2 weeks after administration, except for surgeries under local anesthesia;
• 10\. Administration of live attenuated vaccines within 1 month before dosing;

Other illness

• 5\. Had severe, uncontrolled infection symptoms (bacterial, viral, fungal, etc.) during the screening period;
• 11\. Known severe allergic reaction to QI-019B or any of its formulation components;
• 12\. Known severe allergic reaction to tocilizumab;
• 14\. Other conditions deemed by the investigator to be unsuitable for participation in this study.

Other

• 13\. Unsuitable for establishing intravenous access;

• 1\. Age ≥ 18 years, any gender;
• 2\. Diagnosed with multiple myeloma (MM) according to IMWG diagnostic criteria;
• 3\. Have received at least 2 lines of anti-MM treatment, with at least one full treatment cycle per line, and experienced disease progression during the most recent anti-myeloma treatment or within 12 months after it, confirmed by available clinical evidence; or deemed by the investigator to be refractory to both immunomodulatory agents and proteasome inhibitors, with disease progression during the most recent anti-myeloma treatment or within 2 months after it (according to IMWG diagnostic criteria);
• 4\. Disease must be measurable at screening, meeting one or more of the following criteria:
  • Serum M protein level ≥ 0.5 g/dL;
  • Or urine M protein level ≥ 200 mg/24h;
  • Or involved serum free light chain ≥ 10 mg/dL with abnormal serum free light chain κ/λ ratio;
• 5\. ECOG performance status 0-2, with an expected survival of ≥ 3 months;
• 6\. Bone marrow function test results (from screening or within 2 months prior) meet the following requirements:
  • Hemoglobin ≥ 6 g/dL (no red blood cell transfusion within 1 week before screening), recombinant human erythropoietin allowed; for patients meeting the ≥ 6 g/dL hemoglobin requirement at screening, red blood cell transfusions are allowed to maintain hemoglobin ≥ 6 g/dL;
  • Absolute neutrophil count (ANC) ≥ 600/μL (no use of granulocyte colony-stimulating factor (G-CSF) within 1 week before screening or pegylated G-CSF within 2 weeks before screening);
  • Platelet count ≥ 50,000/μL;
  • Lymphocyte count ≥ 500/μL;
• 7\. Normal renal function: Creatinine clearance (CrCl) (Cockcroft-Gault formula) ≥45 mL/min;
• 8\. Liver function must meet the following criteria:
  • Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤3.0× the upper limit of normal (ULN);
  • Total bilirubin (TBIL) and alkaline phosphatase (AKP or ALP) ≤2.0× ULN (except for congenital hyperbilirubinemia, e.g., Gilbert's syndrome, direct bilirubin ≤1.5× ULN);
  • Albumin ≥3 g/dL;
• 9\. Cardiac function must meet the following criteria:
  • Left ventricular ejection fraction ≥50% (by echocardiography or MUGA scan);
  • No clinically significant pericardial effusion;
  • No clinically significant electrocardiogram abnormalities;
• 10\. Pulmonary function must meet the following criteria:
  • Blood oxygen saturation ≥90% without oxygen supplementation;
• 11\. Women of childbearing potential must have a negative pregnancy test at screening and before drug infusion and must not be breastfeeding.
• 12\. Men and women of childbearing potential must agree to use effective contraception from the time of signing the informed consent until 1 year after the use of the study drug;
• 13\. Men and women of childbearing potential must agree not to donate sperm or eggs (oocytes) or other reproductive cells from the time of signing the informed consent until 1 year after the use of the study drug;
• 14\. The subject or their legal guardian agrees to participate in this clinical trial and signs the informed consent form (ICF), indicating that they understand the purpose and procedures of this clinical trial and are willing to participate in the study.