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OncoMatch/Clinical Trials/NCT06997081

ERd Combination Treatment in Newly Diagnosed Multiple Myeloma

Is NCT06997081 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including Lenalidomide and Dexamethasone for multiple myeloma.

Phase 2RecruitingUniversity of MiamiNCT06997081Data as of May 2026

Treatment: Lenalidomide · Dexamethasone · ElranatamabThe purpose of this study is to determine the effects that Elranatamab in combination with Lenalidomide and Dexamethasone has on participants that have been newly diagnosed with Multiple Myeloma.

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Extracted eligibility criteria

Cancer type

Multiple Myeloma

Performance status

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

Prior therapy

Max 1 prior line

Cannot have received: multiple myeloma therapy

Exception: ≤1 cycle of prior treatment allowed; see protocol for permitted exceptions

Participants receiving >1 cycle of prior treatment or concurrent systemic treatment for MM with the following exceptions: ... Patients with measurable disease who received up to one cycle of any therapy within 60 days with a washout period of 2 weeks from last dose (on a trial or outside a trial) are eligible

Cannot have received: carfilzomib (carfilzomib)

Exception: only for patients with Smoldering Multiple Myeloma (SMM)

Patients with Smoldering Multiple Myeloma (SMM) previously treated with carfilzomib are excluded

Lab requirements

Blood counts

ANC >1.0 K/μL (0.5-1.0 K/μL allowed at investigator discretion if chronic/ethnic neutropenia and no complications); Platelet count >75 K/μL; Hemoglobin >8 g/dL (transfusions allowed if anemia not due to myeloma)

Kidney function

GFR ≥30 mL/min (MDRD or other accepted method) or creatinine clearance measured by 24-hour urine collection

Liver function

Total bilirubin <1.5 X ULN (isolated total bilirubin ≥1.5 X ULN with conjugated [direct] bilirubin <1.5 X ULN is allowed for Gilbert's syndrome); AST/ALT ≤2.5 X ULN

Participants must have adequate organ and marrow function ≤45 days as defined below: ANC >1.0 K cells/μL; Platelet count >75 K cells/μL; Hemoglobin >8 g/dL; Total bilirubin <1.5 X ULN; AST/ALT ≤2.5 X ULN; GFR ≥30 mL/min

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

US trial sites

  • University of Miami · Miami, Florida

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