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OncoMatch/Clinical Trials/NCT06209606

Pilot Study Using Changes in Serum BCMA to Determine Disease Progression in Multiple Myeloma

Is NCT06209606 recruiting? Yes, currently enrolling (May 2026). This Early Phase 1 trial studies multiple treatments including Ruxolitinib Oral Tablet [Jakafi] and Lenalidomide for multiple myeloma.

Early Phase 1RecruitingOncotherapeuticsNCT06209606Data as of May 2026

Treatment: Ruxolitinib Oral Tablet [Jakafi] · Lenalidomide · MethylprednisoloneThis is a phase 1, multicenter, open-label study evaluating the safety and efficacy of ruxolitinib, steroids and lenalidomide among MM patients who currently show progressive disease using BCMA to test progression.

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Extracted eligibility criteria

Cancer type

Multiple Myeloma

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

Min 2 prior lines

Must have received: lenalidomide (lenalidomide)

has received at least 2 prior regimens including lenalidomide, a proteasome inhibitor, and an anti-CD38 antibody

Must have received: proteasome inhibitor

has received at least 2 prior regimens including lenalidomide, a proteasome inhibitor, and an anti-CD38 antibody

Must have received: anti-CD38 antibody

has received at least 2 prior regimens including lenalidomide, a proteasome inhibitor, and an anti-CD38 antibody

Cannot have received: JAK inhibitor (ruxolitinib)

JAK inhibitor including ruxolitinib

Cannot have received: chemotherapy

Chemotherapy within 3 weeks of study drugs

Cannot have received: corticosteroid

Exception: ≤20 mg/daily prednisone or equivalent allowed

Corticosteroids (>20 mg/daily prednisone or equivalent) within 3 weeks of study drugs

Cannot have received: immunotherapy

Immunotherapy, antibody therapy, immunomodulatory drugs, or proteasome inhibitors within 3 weeks of study drugs

Cannot have received: antibody therapy

Immunotherapy, antibody therapy, immunomodulatory drugs, or proteasome inhibitors within 3 weeks of study drugs

Cannot have received: immunomodulatory drug

Immunotherapy, antibody therapy, immunomodulatory drugs, or proteasome inhibitors within 3 weeks of study drugs

Cannot have received: proteasome inhibitor

Immunotherapy, antibody therapy, immunomodulatory drugs, or proteasome inhibitors within 3 weeks of study drugs

Cannot have received: extensive radiation therapy

Exception: localized radiation therapy allowed

Extensive radiation therapy within 28 days before study drugs. Receipt of localized radiation therapy does not preclude enrollment.

Cannot have received: experimental drug or therapy

Use of any other experimental drug or therapy within 28 days of study drugs

Lab requirements

Blood counts

Absolute neutrophil count ≥ 1.5 x 10^9/L (≥ 1.0 x 10^9/L if BM ≥ 70% plasma cells); Platelet count ≥ 75 x 10^9/L (≥ 50 x 10^9/L if BM ≥ 70% plasma cells; if CrCl < 60 mL/min, platelets > 150 x 10^9/L); Hemoglobin ≥ 8.0 g/dL

Kidney function

Calculated or measured CrCl > 60 mL/minute per Cockcroft-Gault

Liver function

Total bilirubin levels ≤ 2.0 mg/dL; AST (SGOT) and ALT (SGPT) ≤ 2 x ULN

Cardiac function

No impaired cardiac function or clinically significant cardiac diseases, including: MI within 6 months, NYHA Class II+ heart failure, uncontrolled angina, significant pericardial disease, severe uncontrolled ventricular arrhythmias, LVEF below institutional normal, ECG evidence of acute ischemia or active conduction system abnormalities

Laboratory test results within these ranges at Screening and confirmed at enrollment prior to drug dosing on Cycle 1, Day 1: Absolute neutrophil count ≥ 1.5 x 10^9/L... Platelet count ≥ 75 x 10^9/L... Hemoglobin ≥ 8.0 g/dL... Calculated or measured CrCl > 60 mL/minute... Total bilirubin levels ≤ 2.0 mg/dL... AST (SGOT) and ALT (SGPT) ≤ 2 x ULN... Serum potassium 3.0 - 5.5 mEq/L

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

US trial sites

  • Berenson Cancer Center · West Hollywood, California

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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