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OncoMatch/Clinical Trials/NCT05900882

SVRd for the Treatment of Newly Diagnosed Multiple Myeloma Patients Presenting With Extramedullary Disease

Is NCT05900882 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies multiple treatments including Selinexor and Bortezomib for multiple myeloma.

Phase 2RecruitingThe First Affiliated Hospital with Nanjing Medical UniversityNCT05900882Data as of Jun 2026Location: China

Treatment: Selinexor · Bortezomib · Lenalidomide · DexamethasoneThe purpose of this study is to evaluate the efficacy and safety of SVRd in NDMM patients presenting with extramedullary disease.

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Extracted eligibility criteria

Treatments studied

Targeted therapy

SelinexorBortezomib

Endocrine / hormonal

Lenalidomide

Other

Dexamethasone

Cancer type

Multiple Myeloma

Demographics

Ages ≤ 75

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Lab requirements

Blood counts

ANC ≥ 1.0×10^9/L, HGB ≥ 75×10^9/L, PLT ≥ 50×10^9/L (≥50% of bone marrow nucleated cells are plasma cells)

Kidney function

creatinine clearance ≥ 30 ml/min

Liver function

ALT and AST < 3 times the upper limit of normal (ULN); serum bilirubin < 1.5 × ULN

Cardiac function

No active, unstable cardiovascular dysfunction: symptomatic ischemia; uncontrolled, clinically significant conduction abnormalities (except antiarrhythmic ventricular tachycardia); NYHA Class III-IV or LVEF <40%; myocardial infarction within 3 months before C1D1

ANC≥1.0*10^9/L, HGB≥75*10^9/L, PLT≥50*10^9/L (≥50% of bone marrow nucleated cells are plasma cells). Significant hepatic dysfunction (ALT and AST ≥ 3 times the upper limit of normal (ULN)). Serum bilirubin≥1.5 × ULN. creatinine clearance <30 ml/min. Active, unstable cardiovascular dysfunction: a. symptomatic ischemia; b. Uncontrolled, clinically significant conduction abnormalities (except antiarrhythmic ventricular tachycardia), but patients with first-degree atrioventricular block or asymptomatic left anterior bundle/right fascicular block cannot be excluded. c. New York Heart Association (NYHA) Class III - IV or left ventricular ejection fraction (LVEF) <40%; d. Myocardial infarction Within 3 months before C1D1.

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT05900882 currently recruiting?

Yes, this trial is currently recruiting patients.

Can patients have received prior systemic therapy?

No. This trial requires treatment-naive patients — prior systemic therapy is an exclusion criterion.

Is there an age limit?

Yes. Patients must be 75 years or younger.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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