Epcoritamab - Genmab/AbbVie
Alternative Names: ABBV-GMAB-3013; Anti-CD3 anti-CD20 bispecific antibody - Genmab/AbbVie; Duobody-CD3-CD20; DuoBody-CD3xCD20; Epcoritamab-bysp; EPKINLY; GEN-3013; TEPKINLYLatest Information Update: 05 Dec 2025
At a glance
- Originator Genmab
- Developer AbbVie; Genmab
- Class Antineoplastics; Bispecific antibodies; Immunotherapies
- Mechanism of Action Antibody-dependent cell cytotoxicity; Cytotoxic T lymphocyte stimulants
-
Orphan Drug Status
Yes - Follicular lymphoma
Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.
- New Molecular Entity Yes
Highest Development Phases
- Marketed Diffuse large B cell lymphoma
- Registered Follicular lymphoma
- Phase II Non-Hodgkin's lymphoma
- Phase I/II B-cell lymphoma; Chronic lymphocytic leukaemia; Haematological malignancies; Richter's syndrome
Most Recent Events
- 05 Dec 2025 Phase I development is still underway for B-cell lymphoma (In infants, In children, In adolescents, In adults, Second-line therapy or greater) in Belgium, USA, Australia, Canada, France, Czech Republic, Germany, Israel, Italy, Japan, South Korea, Netherlands, Russia, Spain, Taiwan and Turkey
- 18 Nov 2025 Registered for Follicular lymphoma (Combination therapy, Second-line therapy or greater) in USA (SC), Puerto Rico (SC)
- 18 Nov 2025 Adverse events and efficacy data from a phase III EPCORE FL-1 trial in Follicular lymphoma released by AbbVie