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: 09 May 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
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Orphan Drug Status
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
- 02 May 2025 Genmab intends to submit supplemental biological application to the US FDA for Epcoritamab in patients with follicular lymphoma (In combination therapy, Second-line therapy or greater) in first half of 2025
- 20 Feb 2025 Registered for Follicular lymphoma (Second-line therapy or greater) in Japan (SC)
- 20 Feb 2025 Efficacy and adverse events data from a phase I/II EPCORE NHL-3 trial in Non-hodgkin's lymphoma released by Genmab