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Elrexfio (elranatamab)

Pfizer · FDA-approved active Monoclonal antibody Verified Quality 74/100

Bispecific antibody binding BCMA on myeloma cells and CD3 on T-cells, causing cytolysis.

Elranatamab-bcmm (ELREXFIO) is a bispecific BCMA-directed T-cell engager approved under accelerated approval for relapsed or refractory multiple myeloma after ≥4 prior lines of therapy. The drug demonstrates dose-proportional pharmacokinetics with a 22-day half-life and 56.2% subcutaneous bioavailability, achieving steady-state exposure by week 48 on biweekly dosing. Key risks include cytokine release syndrome and increased CYP substrate exposure requiring monitoring of narrow-index drugs. Continued approval is contingent upon verification of clinical benefit in confirmatory trials.

At a glance

Generic nameelranatamab
SponsorPfizer
Drug classBispecific antibody
TargetBCMA (B-cell maturation antigen) on plasma cells, plasmablasts, and multiple myeloma cells; CD3 on T-cells
ModalityMonoclonal antibody
Therapeutic areaOncology
PhaseFDA-approved
First approval2023
Annual revenue304

Mechanism of action

Elranatamab-bcmm is a bispecific B-cell maturation antigen (BCMA)-directed T-cell engaging antibody that functions as a bridge between BCMA-expressing multiple myeloma cells and CD3-expressing T-cells. By binding simultaneously to both targets, the drug brings T-cells into close proximity with myeloma cells, leading to T-cell activation and cytolysis of BCMA-expressing cells. The mechanism involves activation of T-cells, proinflammatory cytokine release, and subsequent multiple myeloma cell lysis.

Approved indications

Common side effects

Drug interactions

Primary sources

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SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
SEC EDGARRevenue + earnings

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