Tepkinly

epcoritamab · AbbVie Deutschland GmbH & Co. KG
CONDITIONAL APPROVAL AUTHORISED IN THE EU

What Tepkinly is used for

Tepkinly as monotherapy is indicated for the treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) after two or more lines of systemic therapy. Tepkinly in combination with lenalidomide and rituximab is indicated for the treatment of adult patients with relapsed or refractory follicular lymphoma (FL). Tepkinly as monotherapy is indicated for the treatment of adult patients with relapsed or refractory follicular lymphoma (FL) after two or more lines of systemic therapy.

Approved use, as published by the European Medicines Agency.

What the labels mean

  • Conditional approval: approved on less complete data because the need is high; more data must follow.

Key facts

Brand
Tepkinly
Active substance
epcoritamab
Disease area
Lymphoma, Large B-Cell, Diffuse
Medicine group
Antineoplastic agents
ATC code
L01FX27
Marketing authorisation holder
AbbVie Deutschland GmbH & Co. KG
Authorised in the EU since
2023

Official information

In the USA

Same active substance: Epkinly

Specialist medicine: started and supervised by a specialist doctor or hospital. This page is a plain-language summary of public official information, not medical advice; follow your doctor and the official product information.

Common questions

What is Tepkinly used for?

Tepkinly as monotherapy is indicated for the treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) after two or more lines of systemic therapy. Tepkinly in combination with lenalidomide and rituximab is indicated for the treatment of adult patients with relapsed or refractory follicular lymphoma (FL). Tepkinly as monotherapy is indicated for the treatment of adult patients with relapsed or refractory follicular lymphoma (FL) after two or more lines of systemic therapy.

What is the active substance in Tepkinly?

Tepkinly contains epcoritamab.

Who makes Tepkinly?

The EU marketing authorisation holder is AbbVie Deutschland GmbH & Co. KG.

Source: European Medicines Agency medicines data (ema.europa.eu), reproduced with acknowledgement of the source. Page made 5 November 2026 by Satya Babu.

← All specialty medicines, EU

For information only, not medical advice. This page is a plain-language summary written from standard prescribing information and the public guides linked below. Brands sometimes change their formula, so always check the composition printed on the pack. Doses here are typical adult doses; yours may differ. Do not start, stop or change a medicine without your doctor or pharmacist, and keep all medicines away from children. In an emergency, call 112 (India) or your local emergency number.