Elranatamab

ELREXFIO®

Overview

Elranatamab is a B-cell Maturation Antigen (BCMA)-CD3 bispecific antibody being tested in multiple myeloma.

SparkCures ID 302
Developed By Pfizer
Brand Name Elrexfio®
Generic Name Elranatamab
Additional Names PF-06863135
Treatment Classifications
Treatment Targets
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Clinical Trials

All Clinical Trials

View all active clinical trials around the US.

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Untreated / Newly Diagnosed Multiple Myeloma

The following is a listing of clinical trials for patients with multiple myeloma who have been newly diagnosed or have not yet received treatment.

Early Relapse Multiple Myeloma

The following is a listing of clinical trials for patients with multiple myeloma who have received one to two prior lines of therapy.

Late Relapse Multiple Myeloma

The following is a listing of clinical trials for patients with multiple myeloma who have received three or more prior lines of therapy.

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Smoldering Myeloma
Monoclonal Gammopathy of Undetermined Significance (MGUS)

Published Results

Elranatamab Shows Activity, Safety as Compassionate Use in R/R Multiple Myeloma

August 13, 2024

Real-world data presented at the 2024 EHA Congress revealed at a median follow-up of 15.5 months (range, 3.4-18.8), a heavily pretreated population of patients with relapsed/refractory multiple myeloma administered elranatamab (n = 101) achieved an overall response rate (ORR) of 51.5%, including a very good partial response (VGPR) or better rate of 42%. Notably, 22% of patients experienced a VGPR or better after 1 cycle of treatment.

Additional data showed the median duration of response (DOR) was 11 months (95% CI, 8–not applicable), and 1-year DOR rate was 48% (95% CI, 31.1%-64%). The median overall survival (OS) was 10.1 months (95% CI, 6.79-13), and the 1-year OS rate was 41.9% (95% CI, 31.7%-52.1%).

Regarding safety, the rates of grade 1 and 2 cytokine release syndrome (CRS) were 35% and 10%, respectively, and no instances of grade 3 or higher CRS were reported. Grade 1, grade 2, and grade 5 immune effector cell–associated neurotoxicity syndrome occurred in 1 patient (1%) each. The rates of any-grade infections and serious grade 3 or higher infections were 49% and 24%, respectively.

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