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Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.

Contact Information:

Rebekah Taylor (847) 937-8000
rebekah.taylor@abbvie.com


Study Location:

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Be Part of Research - Trial Details - Real-World Study to Assess Subcutaneous Epcoritamab in Adult Participants With Diffuse Large B-Cell and Follicular Lymphoma

Real-World Study to Assess Subcutaneous Epcoritamab in Adult Participants With Diffuse Large B-Cell and Follicular Lymphoma

Recruiting

Open to: ALL

Age: 18.0 - N/A

Medical Conditions

Diffuse Large B-cell Lymphoma
Follicular Lymphoma


This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


Diffuse large B-cell lymphoma (DLBCL) is an aggressive and rare cancer of a type of immune cells (a white blood cell responsible for fighting infections) and the most common type of non-Hodgkin lymphoma. Follicular Lymphoma (FL) is a slow-growing type of non-Hodgkin lymphoma. The purpose of this study is to assess the real-world effectiveness of subcutaneous epcoritamab in adult participants with advanced DLBCL and FL.

Epcoritamab is an investigational drug being developed for treating participants with DLBCL and FL. Approximately 700 participants will be enrolled in approximately 80 sites across 12-20 countries globally.

Participants will receive epcoritamab as prescribed by their physician in accordance with local country label. Participants will be followed for up to 3 years.

There is expected to be no additional burden for participants in this trial. Participants will attend regular visits during the study at a hospital or clinic according to their routine clinical practice.

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

Mar 2025 Sep 2031

OBSERVATIONAL



You can take part if:



You may not be able to take part if:


This is in the inclusion criteria above


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • Milton Keynes Hospital /ID# 272817
    Milton Keynes
    Buckinghamshire
    MK6 5LD
  • Royal Cornwall Hospital /ID# 272747
    Truro
    Cornwall
    TR1 3LQ
  • Cheltenham General Hospital /ID# 272746
    Cheltenham
    Gloucestershire
    GL53 7AN
  • The Newcastle Upon Tyne Hospitals NHS Foundation Trust /ID# 272748
    Newcastle upon Tyne
    NE3 3HD
  • Queen Alexandra Hospital /ID# 272744
    Portsmouth
    Hampshire
    PO6 3LY
  • NHS Lanarkshire /ID# 276471
    Airdrie
    North Lanarkshire
    ML6 0JS
  • Nottingham City Hospital /ID# 272753
    Nottingham
    Nottinghamshire
    NG5 1PB
  • The Christie /ID# 272745
    Manchester
    M20 4BX


The study is sponsored by AbbVie and is in collaboration with Genmab.




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Read full details for Trial ID: NCT06830759
Last updated 12 February 2026

This page is to help you find out about a research study and if you may be able to take part

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