Single-arm, Open-label, Early-stage Clinical Study of UTAA17 Injection in the Treatment of Relapsed/Refractory Multiple Myeloma
The clinical trial was designed as a single-arm, open-label clinical study, with the main purpose of exploring the safety, pharmacokinetics, and best recommended dose (RP2D) of the UTAA17 injection in the treatment of relapsed or refractory multiple myeloma (r/r MM) subjects, and also the efficacy will be observed. Eligible subjects will accept the infusion of UTAA17 injection after pretreatment, and their blood will be collected before and after infusion for evaluation of pharmacokinetics, immunogenicity and safety. This study plans to evaluate efficacy using the revised Evaluation of Efficacy in multiple myeloma -IMWG criteria (2016), which will be evaluated at 4w, 2m, 3m, 6m, and 6 to 24m (at a frequency of Q3m) after cell reinfusion, in addition to the baseline period. Efficacy evaluation continues until one of the following occurs: subject disease progression (PD), acceptance of a new antitumor therapy, death, occurrence of intolerable toxicity, investigator decision, or patient decision to withdraw.
• All subjects or legal representatives must sign an informed consent form approved by the Ethics Committee in person before commencing any screening process.
• ≥18 years old, regardless of gender, diagnosed with relapsed or refractory multiple myeloma according to the Efficacy Evaluation Criteria for multiple myeloma (IMWG), where relapsed or refractory is defined as: Multiple myeloma that has failed or relapsed after at least 3 lines of therapy (including proteasome inhibitor and immunomodulator-based chemotherapy regimen) in which induction chemotherapy, stem cell transplantation, and maintenance therapy given consecutively are considered a treatment regimen if no disease progression occurs during treatment.
• The presence of measurable lesions at the time of screening will be determined according to any of the following criteria:
‣ Monoclonal plasma cells in bone marrow ≥ 10%.
⁃ Serum monoclonal protein (M-protein) level ≥10 g/L.
⁃ Urinary M protein level ≥200 mg/24 hours.
⁃ Light chain multiple myeloma with no measurable lesions in serum or urine: serum immunoglobulin free light chain ≥10 mg/dL and abnormal serum immunoglobulin κb /γ free light chain ratio.
⁃ There are extramedullary lesions.
• BCMA expression on the cell membrane is positive by flow cytometry and/or immunohistochemistry.
• Patients were unable to undergo autologous hematopoietic stem cell transplantation or relapsed after autologous hematopoietic stem cell transplantation and were determined by the investigators to require treatment.
• Patients who have previously received CAR T cell therapy should not be included until at least 3 months after the last CAR T cell infusion and no previously used CAR T cells are detectable in peripheral blood or bone marrow.
• The ECOG score is 0 or 1.
• Expected survival ≥12 weeks.
• Subjects must have appropriate organ function and meet all of the following laboratory test results prior to enrollment
‣ Blood routine: Absolute neutrophil count (ANC) \>0.75×10\^9 /L; Absolute lymphocyte count (ALC) ≥0.3×10\^9 /L; Platelet ≥50×10\^9 /L; Hemoglobin \>60 g/L
⁃ Liver function: alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤2.5 × upper limit of normal (ULN); Serum total bilirubin ≤1.5×ULN, except patients with Gilbert syndrome (patients with Gilbert syndrome ≤3.0 times the upper limit of normal and direct bilirubin ≤1.5 times the upper limit of normal can be included)
⁃ Renal function: serum creatinine ≤2.5×ULN
⁃ Coagulation function: fibrinogen ≥ 1.0g /L; Activated partial thromboplastin time, activated partial thromboplastin time ≤1.5×ULN, and prothrombin time (PT) ≤1.5×ULN
⁃ Must have a minimum level of lung reserve, blood oxygen saturation \> 92%
• Hemodynamically stable and left ventricular ejection fraction (LVEF) ≥ 50% as determined by echocardiography.