BLASUBCUTANEOUSINJECTABLEPriority Review
Approved
May 2023
Lifecycle
Growth
Competitive Pressure
30/100
Data completeness
4/8 — Partial
Priority Review
EPKINLY (epcoritamab-bysp) by Genmab is cd20-directed antibody interactions [moa]. Approved for diffuse large b-cell lymphoma, follicular lymphoma. First approved in 2023.
Drug data last refreshed 23h ago · AI intelligence enriched 1w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
EPKINLY (epcoritamab-bysp) is a bispecific CD20-directed CD3 T cell engager approved by the FDA on May 19, 2023, for relapsed or refractory diffuse large B-cell lymphoma (DLBCL) and follicular lymphoma (FL). It works by simultaneously binding to CD20 on B-cell lymphoma cells and CD3 on T cells, redirecting T-cell killing activity against malignant B cells. The drug is administered subcutaneously, offering a practical delivery advantage over IV agents.
Growth
EPKINLY is in early growth phase post-approval with moderate competitive pressure (30%), creating opportunities for team expansion across commercial and clinical operations functions.
Mechanism of Action
CD20-directed Antibody Interactions
Pharmacologic Class:
Bispecific CD20-directed CD3 T Cell Engager
Indications (2)
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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.