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

Sponsor: AbbVie

NCT ID: NCT06830759

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Health checks and monitoring — no treatment given
Type of study
Observational (no treatment given)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Not specified by the sponsor
How long the study runs
Study runs about 78 months (dates as stated)
About the drug or intervention
Not specified by the sponsor
Patient visit burden
Not specified by the sponsor

In plain English

This study looks at how a medicine called epcoritamab works in real-world care for adults with two types of blood cancer: diffuse large B-cell lymphoma and follicular lymphoma. It is run by AbbVie. People in this study have already had two or more earlier courses of treatment.

Who can take part

  • Adults due to be treated with epcoritamab after two or more earlier courses of treatment for diffuse large B-cell lymphoma or follicular lymphoma.
  • Epcoritamab must be given as set out in the approved medicine information for the country taking part.
  • The doctor must have already decided to treat the person with epcoritamab before they were asked to join the study.

Who may not be able to

  • Any condition listed as a reason not to take epcoritamab in the approved medicine information for that country.
  • Taking part at the same time in another clinical trial that tests a treatment (surveys, registries and observational studies are allowed).

What taking part involves

  • • Not stated — ask the trial team.

Time commitment: Not stated — ask the trial team.

Plain-English summary (AI-generated) from registry data. Not eligibility advice — only the trial team can confirm whether you can take part. Use the eligibility checker to see how your health profile matches this trial.

Type of study
Observing health over time
Ages
18 Years and over
Who
All
Number of participants
700
Started
2025-03-28
Last checked
2026-02

Plain English Summary

What is this study?

  • • Testing a new treatment for diffuse large b-cell lymphoma
  • • Clinical study - 700 participants
  • • 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

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with diffuse large b-cell lymphoma

Where?

  • • Milton Keynes - Milton Keynes Hospital /ID# 272817
  • • Truro - Royal Cornwall Hospital /ID# 272747
  • • Cheltenham - Cheltenham General Hospital /ID# 272746
  • • Portsmouth - Queen Alexandra Hospital /ID# 272744
  • • +4 more UK sites

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

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.

Diffuse Large B-cell LymphomaFollicular Lymphoma

How this trial compares with your answers

Answer 2 more questions to improve match

What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: All genders

What the study is looking for

  • ✓Participants who are scheduled to be treated with epcoritamab for Treatment after two or more previous treatments...
  • ✓Treatment with epcoritamab should be administered in accordance with the approved local label in the participating...
  • ✓The decision to treat the participant should have been made by the clinician prior to, and independently of any...

Who cannot take part

  • ✗Any condition included in the contraindications section of the approved local epcoritamab label in the participating...
  • ✗Participation in a concurrent interventional clinical trial (not including non-interventional/ observational study,...
See the full criteria
Inclusion Criteria: * Participants who are scheduled to be treated with epcoritamab for Treatment after two or more prior lines of therapy 3L+ diffuse large B-cell lymphoma ((D)LBCL) or 3L+ Follicular lymphoma (FL). * Treatment with epcoritamab should be administered in accordance with the approved local label in the participating country. * The decision to treat the participant should have been made by the clinician prior to, and independently of any decision to approach the participant to participate in this study. Exclusion Criteria: * Any condition included in the contraindications section of the approved local epcoritamab label in the participating country. * Participation in a concurrent interventional clinical trial (not including non-interventional/ observational study, PMOS, or registry participation) from enrollment and throughout the study.

Where Is This Study? (8 UK sites)

Milton Keynes Hospital /ID# 272817

Milton Keynes MK6 5LD, United Kingdom

Recruiting
Hospital R&D contact (matched)

Antoanela Colda

Antoanela.colda@mkuh.nhs.uk01908 995119 / 01908 996651

Royal Cornwall Hospital /ID# 272747

Truro TR1 3LQ, United Kingdom

Recruiting
Hospital R&D contact (matched)

Abi Weeks

rch-tr.CornwallResearch@nhs.net01872 25 6424

Cheltenham General Hospital /ID# 272746

Cheltenham GL53 7AN, United Kingdom

Recruiting

Queen Alexandra Hospital /ID# 272744

Portsmouth PO6 3LY, United Kingdom

Recruiting

NHS Lanarkshire /ID# 276471

Airdrie ML6 0JS, United Kingdom

Recruiting

Nottingham City Hospital /ID# 272753

Nottingham NG5 1PB, United Kingdom

Recruiting
Hospital R&D contact (matched)

Alison Lloyd

nuhnt.researchsponsor@nhs.net0115 9249924

The Christie /ID# 272745

Manchester M20 4BX, United Kingdom

Recruiting
Hospital R&D contact (matched)

Research and Innovation Office

the-christie.ri@nhs.net---

The Newcastle Upon Tyne Hospitals NHS Foundation Trust /ID# 272748

Newcastle upon Tyne NE3 3HD, United Kingdom

Recruiting
Hospital R&D contact (matched)

Research and Development

nuth.genericqueries@nhs.net0191 282 4926

How to Get in Touch

Rebekah Taylor

Sponsor contact

CONTACT

(847) 937-8000 rebekah.taylor@abbvie.com
Data sourced from ClinicalTrials.gov · Last verified: 2026-02