Wednesday, July 8, 2026

Drug profile · INN

epcoritamab-bysp

epcoritamab-bysp (EPKINLY) is a b-lymphocyte antigen cd20 binding agent. Route of administration: subcutaneous. Current US regulatory status: approved.

FDA: approved
US status approved
Patents linked 0
Pipeline programs 2
News articles 0
Drug details — epcoritamab-bysp
US status
approved
Class
Route
SUBCUTANEOUS
Patents
0
Programs
2
Data quality
0.84

Quick answer

epcoritamab-bysp (EPKINLY) is a b-lymphocyte antigen cd20 binding agent. Route of administration: subcutaneous. Current US regulatory status: approved.

Key facts

INN epcoritamab-bysp
Brand EPKINLY
Mechanism B-lymphocyte antigen CD20 binding agent
Target B-lymphocyte antigen CD20
Route SUBCUTANEOUS
Formulation INJECTABLE

Mechanism of action

B-lymphocyte antigen CD20 binding agent

Primary target: B-lymphocyte antigen CD20

Approval history

Authority Status Date
FDA approved

Pipeline programs

  1. Epcoritamab Phase 2 · United Therapeutics Europe · Diffuse Large B-Cell Lymphoma, Not Otherwise Specified
  2. Epcoritamab Phase 2 · ADC Therapeutics · Large B-cell Lymphoma

Related & competitor drugs

  1. odronextamab Nervous system (NOT)
  2. ublituximab-xiiy B-lymphocyte antigen CD20 binding agent
  3. glofitamab-gxbm B-lymphocyte antigen CD20 binding agent
  4. mosunetuzumab-axgb B-lymphocyte antigen CD20 binding agent
  5. obinutuzumab Antineoplastic and immunomodulating agents (L01)
  6. ocrelizumab Antineoplastic and immunomodulating agents (L04)

Frequently asked questions

What is epcoritamab-bysp?

epcoritamab-bysp (EPKINLY) is a b-lymphocyte antigen cd20 binding agent. Route of administration: subcutaneous. Current US regulatory status: approved.

What is the brand name for epcoritamab-bysp?

EPKINLY is a marketed brand name for epcoritamab-bysp. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of epcoritamab-bysp?

epcoritamab-bysp has approved status in the United States according to our Drugs@FDA-derived records. Verify on the official FDA label before clinical or commercial decisions.