BLAINJECTIONSOLUTIONPriority Review
Approved
Aug 2023
Lifecycle
Growth
Competitive Pressure
30/100
Clinical Trials
20
Data completeness
4/8 — Partial
Priority Review
Drug data last refreshed 1h ago · AI intelligence enriched 6d ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
ELREXFIO (elranatamab-bcmm) is a bispecific antibody approved by the FDA in August 2023 for hematologic malignancies. It functions as a B-cell maturation antigen (BCMA)-targeted bispecific T-cell engager, designed to redirect T cells to kill cancer cells expressing BCMA. The drug is administered as an intravenous injection solution.
Growth
Early-stage growth product with moderate competitive pressure (30) signals expanding commercial infrastructure and increasing team hiring in hematology oncology.
Mechanism of Action
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (20)
A Study of Elranatamab Outpatient Administration in Patients With Relapsed/Refractory Multiple Myeloma
Started Aug 2026
46 enrolled
Multiple Myeloma (MM)Multiple Myeloma RefractoryMultiple Myeloma in Relapse+1 more
A Phase 2 Study of Radiotherapy-induced Immune Priming to Enhance Elranatamab (Elra) in Relapsed Refractory Multiple Myeloma (RRMM) With Extramedullary Disease (EMD) and Paramedullary Disease (PMD) "PRIME-EMD-PMD"
Started Mar 2026
34 enrolled
Phase 2Radiotherapy-Induced Immune PrimingElranatamab+4 more
ASPIRE: A Registry Study Of Chinese Patients With TCE-RRMM Treated By Elranatamab
Started Dec 2025
159 enrolled
TCE-RRMM
Frontline T-cell Engager vs Autologous Stem Cell Transplant (ASCT) and Measurable Residual Disease (MRD)-Guided Sequential Intensification thERapy in Multiple Myeloma
Started Aug 2025
100 enrolled
Multiple Myeloma, Newly DiagnosedMultiple Myeloma (MM)
Korean Post Marketing Surveillance for ELREXFIO (Elranatamab).
Started Jun 2025
150 enrolled
Multiple Myeloma
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.