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BCMA/CD3 BsAb in the Treatment of High-risk Smoldering Multiple Myeloma

RecruitingNAAges 18 Years - 78 YearsAllInstitute of Hematology & Blood Diseases Hospital…
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In plain words

What the trial is, and whether it could suit you

The purpose of this study is to evaluate the safety and efficacy of CM-336, which is a BCMA/CD3 BiTE, in the treatment of high risk smoldering multiple myeloma.

Sign in to get the eligibility rules as simple questions to take to your doctor.

📋 Eligibility rules (as published)
Inclusion Criteria: 1. Know and voluntarily sign an informed consent form (ICF). 2. Age ≥18 years. 3. Definite diagnosis of SMM: According to IMWG Criteria 10, the patient must have histologically or cytologically confirmed smoldering multiple myeloma (SMM), including: 1. Serum M protein ≥3 g /dL and/or BMPCs≥10%(but not more than 60%) 2. No anemia: hemoglobin ≥10 g /dL 3. No renal failure: serum creatinine ≥2.0 mg/dL 4. No hypercalcemia: calcium ≥10.5 mg/dL 5. dissolving bone lesions without radiographic indications: X-ray, CT, or positron emission tomography (PET)/CT without dissolving bone lesions, with no more than 1 lesion on whole-body MRI (Note: In the investigator's judgment, whole-body CT or PET/CT may replace MRI for patients with contraindications or for whom MRI is not available). 6. FLC ratio \<100 (unless light chain ≤10 mg /dL is involved) Note: Anemia, renal failure and hypercalcemia are allowed if there is evidence that anemia, renal failure, hypercalcemia or bone lesions are not associated with multiple myeloma (MM). 4. High-risk SMM are defined as meeting one or more of the three criteria in the following part: (i) Mayo 2018, (ii) IMWG 2020 and (iii) evolving pattern. (i)Mayo 2018 * M protein \> 2 g/dL ② The ratio of affected to unaffected FLC was \> 20 ③BMPC \> 20% of the 3 items meet any 2 or more (ii) IMWG 2020 * FLC ratio 0-10: 0 points 10-25: 2 points 25-40: 3 points \>40: 5 points ②M protein (g/dL) 0-1.5: indicates 0 points 1.5-3: 3 points \>3: 4 points ③BMPC (%) 0-15: 0 points 15-20: 2 points 20-30: 3 points 30-40: 5 points \>40: 6 points ④FISH \* : Yes: 2 points None: 0 points The sum of the four points is greater than or equal to 9 (iii)Progression model * Necessary condition: BMPC\>10% ② Sufficient conditions: a. Serum M protein \>3 g/dL b. IgA type SMM c. Immune paralysis (reduction of two uninvolved homologous immunoglobulins) d. The proportion of free light chain (FLC) in serum that is affected/not affected \> 8 (but \<100) e.M protein level increased (SMM type increased; Serum M protein level was increased by ≥25% twice in 6 months. F.BMPC: 50%-59% g. Abnormal plasma cell immunophenotype (95% + of cloned BMPC) and reduction of one or more uninvolved immunoglobulin types. h.≥5% of cells had chromosomal abnormalities (t (4,14) or del 17 p or 1 q acquisition i. Increased circulating plasma cells (PCs\>5×106/L or 5%) j. Merri indicates diffuse abnormalities or 1 focal lesion, and/or increased uptake of focal lesion in PET-CT class without underlying osteolytic osteopathy. Meet the necessary conditions, 1 or more sufficient conditions. \*FISH exceptions are defined as the presence of any of the following: t (4,14), t (14,16), 1 q amplification, del 13 qt, t (4,20) 5. ECOG physical status score ≤2 points. 6. Meeting the following laboratory indicators within 28 days prior to study participation: a. neutrophils absolute value (ANC) \>1000/ml b. Platelet count (PLC)\> 75,000 /ml c. Total bilirubin ≤2 mg/dL d. Glutamic oxalic aminotransferase (AST) \<2.5 times the conventional upper limit (ULN) e. Alanine aminotransferase (ALT) \<2.5 times the upper limit of normal (ULN) f. Estimated creatinine clearance (CLcr)≥60 mL/min. 7. Non-childbearing women meet the entry requirements; Female patients of childbearing age must have a negative serum (beta-human chorionic gonadotropin) or urine pregnancy test at the time of screening. 8. Men, women of childbearing age, and their partners voluntarily use contraception deemed effective by investigators during treatment and for at least three months after CAR T cell transfusion. 9. Male patients must agree not to donate sperm from the initial screening period until 90 days after the last medication. 10. Patients must be willing and able to complete study procedures and follow-up examinations. Note: Fertile women are all women who have begun menstruating and are not in late menopause and who have not undergone surgical sterilization (e.g., hysterectomy, bilateral tubal ligation, bilateral oophorectomy). Postmenopause is defined as more than 12 consecutive months of amenorrhea for an unspecified reason. Women who are using mechanical birth control methods such as oral contraceptives or intrauterine devices should be considered fertile. Male subjects (including those who have undergone vasectomy) must consent to the use of condoms during sex with women of childbearing age and must not plan to impregnate the woman during the study drug use period from the date of signing the informed consent form and within 3 months after the last study drug receipt. Exclusion Criteria: 1. Diagnosis of symptomatic multiple myeloma: refer to the Chinese Guidelines for Diagnosis and Treatment of multiple myeloma (revised in 2022); 2. Along with other tumors that must be treated. 3. Previously received immunotherapy against BCMA targets. 4. The researchers judged that BCMA/CD 3 dual antibody therapy is not suitable, such as severe cardiopulmonary disease and other conditions that are not suitable for BCMA/CD 3 dual antibody therapy. 5. Received SMM treatment within six months. 6. Known intolerance, allergy or contraindications to BCMA/CD 3 dual anti-active ingredients. 7. Patients with unstable or active cardiovascular and cerebrovascular diseases meet any of the following criteria: 1. Unstable angina pectoris, symptomatic myocardial ischemia, myocardial infarction, or coronary artery reconstruction had occurred within 180 days prior to initial administration. 2. Uncontrolled hypertension (\>140/90 MMHG, with a blood pressure fluctuation of more than 180/100 MMHG over 6 months); 3. Uncontrolled and clinically significant conduction abnormalities (e.g., patients with ventricular arrhythmias controlled by antiarrhythmic drug therapy), not excluding patients with first-degree AV block or asymptomatic left anterior bundle branch block/right bundle branch block (LAFB/RBBB);
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What it tests

  • CM336
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Where

1 site
Institute of Hematology and Blood Diseases Hospital Chinese Academy of Medical Sciences
Tianjin, China
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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