Last updated: August 10, 2022
Sponsor: Samsung Medical Center
Overall Status: Active - Recruiting
Phase
2
Condition
Lymphoproliferative Disorders
Cancer
Multiple Myeloma
Treatment
N/AClinical Study ID
NCT05497102
SMC 2019-12-037
Ages 20-70 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Age 20~70
- Progressive disease after 1st ASCT
- Duration of response after 1st ASCT > 12 months
- Measurable disease (+)
- Serum M-protein ≥ 1 g/dL
- Urine M-protein ≥ 200 mg/24 hr
- Serum Free Light Chain(FLC) assay: involved FLC level ≥10 mg/dL (serum Free LightChain ratio is abnormal)
- Adequate organ function for induction & ASCT
- Absolute Neutrophil Count (ANC) ≥ 1.0 x 109/L
- Platelets ≥ 50 x 109/L (≥ 30 x 109/L if myeloma involvement is > 50% in the bonemarrow)
- Hemoglobin ≥ 8.0 g/dL
- Creatinine clearance ≥ 30 mL/minute
- Serum Bilirubin ≤ 1.5 x upper limit of normal
- Aspartate aminotransferase(AST) and Alanine aminotransferase(ALT) ≤ 3 x upperlimit of normal
- Eastern Cooperative Oncology Group performance scale 0~2
- Survival expectancy > 3 months
- Adequately controlled hepatitis B(HBV) & hepatitis C(HCV)
- Written informed consent
- Optimal contraceptions
Exclusion
Exclusion Criteria:
- Prior refractoriness or intolerance to carfilzomib
- Prior refractoriness or intolerance to lenalidomide/dexamethasone
- Any treatment after progressive disease after 1st ASCT. High-dose dexamethasone orpalliative radiation is permitted.
- Waldenstroem's macroglobulinemia, POEMS syndrome, or plasma cell leukemia
- Pregnant or nursing lactating women
- Myocardial infarct within 6 months, heart failure of New York Heart Association(NYHA)Class III~IV, uncontrolled ventricular arrhythmia, severe coronary arterialobstructive disease
- Uncontrolled hypertension (Defined as an average systolic blood pressure >= 160 mmHgor diastolic >= 100 mmHg) or diabetes
- Grade 3~4 neuropathy
- HIV infection
- Severe or uncontrolled medical conditions, laboratory abnormalities, or psychiatricdisorders that may preclude the participation of the study by the physician'sdiscretion
- Contraindication to any of the required concomitant drugs or supportive treatments,including hypersensitivity to all anticoagulation and antiplatelet options, antiviraldrugs, or intolerance to hydration due to preexisting pulmonary or cardiac impairment
- Diagnosis of other malignant disease other than myeloma within 5 year. Exceptions areproperly treated non-melanomatous skin cancers, cervical intraepithelial neoplasia,prostate cancer that do not require treatment, or properly excised well-differentiatedthyroid cancers
Study Design
Total Participants: 58
Study Start date:
November 08, 2021
Estimated Completion Date:
December 31, 2025
Study Description
Connect with a study center
Samsung Medical Center
Seoul,
Korea, Republic ofActive - Recruiting
Not the study for you?
Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.