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OncoMatch/Clinical Trials/NCT06421675

Outpatient and Intermittent Dosing of Elranatamab in Relapsed/Refractory Multiple Myeloma

Is NCT06421675 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies Elranatamab for refractory multiple myeloma.

Phase 2RecruitingOntario Clinical Oncology Group (OCOG)NCT06421675Data as of May 2026

Treatment: ElranatamabA phase II study of single agent elranatamab in patients with relapsed and/or refractory multiple myeloma (MM) who have previously received at least three classes of therapeutic agents and are refractory to the last line of treatment. The primary objective of this study is to improve the tolerability and safety of elranatamab in patients with relapsed and/or refractory multiple myeloma by evaluating an outpatient and intermittent dosing strategy.

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Extracted eligibility criteria

Cancer type

Multiple Myeloma

Performance status

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

Prior therapy

Min 3 prior lines

Must have received: immunomodulatory drug (lenalidomide, pomalidomide)

An immunomodulatory drug (lenalidomide or pomalidomide)

Must have received: proteasome inhibitor (bortezomib, ixazomib, carfilzomib)

a proteasome inhibitor (bortezomib, ixazomib, carfilzomib)

Must have received: anti-CD38 drug (daratumumab, isatuximab)

an anti-CD38 drug (daratumumab or isatuximab)

Cannot have received: BCMA targeting agent

History of prior treatment with a BCMA targeting agent

Cannot have received: stem cell transplant

Exception: within 12 weeks prior to enrollment or active graft versus host disease

Stem cell transplant within 12 weeks prior to enrollment or active graft versus host disease

Lab requirements

Blood counts

Absolute neutrophil count (ANC) ≤ 1.0 x 10^9 /L; Platelet count ≤ 25 x 10^9 /L; Hemoglobin ≤ 8.0 g/dL

Kidney function

Creatinine clearance < 30 mL/min (according to the Cockcroft Gault formula, by 24-hour urine collection for creatinine clearance, or according to local institutional standard method)

Liver function

Serum AST and ALT > 2.5 x upper limit of normal (ULN); Total bilirubin > 2.0 x ULN (≥ 3.0 unless known to have Gilbert's disease)

Laboratory results ... ANC ≤ 1.0 x 10^9 /L ... Platelet count ≤ 25 x 10^9 /L ... Hemoglobin ≤ 8.0 g/dL ... Serum AST and ALT > 2.5 x ULN ... Creatinine clearance < 30 mL/min ... Total bilirubin > 2.0 x ULN (≥ 3.0 unless known to have Gilbert's disease)

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

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