Diffuse Large B-cell LymphomaEpcoRealNCT06830759
Real-World Study to Assess Subcutaneous Epcoritamab in Adult Participants With Diffuse Large B-Cell and Follicular Lymphoma
An observational study of Diffuse Large B-cell Lymphoma and Follicular Lymphoma, run by AbbVie at 73 sites in 13 countries.
Trial summary
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. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Diffuse Large B-cell Lymphoma, Follicular Lymphoma
- How many people
- 700 participants
- Where
- 73 sitesin 13 countries
- Study dates
- 28 Mar 2025to Sep 2031
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Adult participants who are being treated with epcoritamab for Diffuse Large B-Cell and Follicular Lymphoma
Who may be able to join
- 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.
Who cannot join
- 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.
Trial locations and contacts
73 sites in 13 countries. Contact the study team or a site near you to ask about taking part.
73 sites in 13 countries
Spain12 sites, 12 recruiting
- Recruiting
Complejo Hospitalario Universitario A Coruña /ID# 272040
A Coruña, A Coruna, 15006
- Recruiting
Institut Català d'Oncologia (ICO) - Badalona /ID# 272043
Badalona, Barcelona, 08916
- Recruiting
Hospital Universitario De Burgos /ID# 272066
Burgos, 09006
- Recruiting
Hospital Universitario Reina Sofia /ID# 272051
Córdoba, Cordoba, 14004
- Recruiting
Hospital de Manises /ID# 272046
Manises, Valencia, 46940
- Recruiting
Hospital Costa del Sol /ID# 272431
Marbella, Malaga, 29603
- Recruiting
Hospital General Universitario Morales Meseguer /ID# 272466
Murcia, 30008
- Recruiting
Hospital Universitario de Navarra /ID# 272041
Pamplona, Navarre, 31008
- Recruiting
Hospital Universitari Parc Tauli /ID# 272044
Sabadell, Barcelona, 08208
- Recruiting
Hospital Universitario Nuestra Señora de Candelaria /ID# 272413
Santa Cruz de Tenerife, 38010
- Recruiting
Hospital Universitario de Valme /ID# 272050
Seville, Sevilla, 41014
- Recruiting
Hospital Clinico Universitario de Valladolid /ID# 272042
Valladolid, 47003
Greece11 sites, 11 recruiting
- Recruiting
University General Hospital of Alexandroupoli /ID# 272737
Alexandroupoli, Evros, 68100
- Recruiting
Evangelismos Hospital /ID# 272736
Athens, Attica, 10676
- Recruiting
General Hospital of Athens Laiko /ID# 272758
Athens, Attica, 11527
Site Coordinator, +30 213 2061702
- Recruiting
University General Hospital Attikon /ID# 272738
Athens, Attica, 12462
- Recruiting
University Hospital of Ioannina /ID# 272739
Ioannina, 45500
- Recruiting
Agios Andreas Hospital Patras /ID# 273629
Pátrai, Achaia, 26335
Site Coordinator, +30 2613601130
- Recruiting
Metaxa Cancer Hospital Of Piraeus /ID# 273623
Piraeus, Attica, 18537
Site Coordinator, +30 213 2079100
- Recruiting
AHEPA University General Hospital of Thessaloniki /ID# 273633
Thessaloniki, 54636
Site Coordinator, +30 231 330 3110
- Recruiting
General Hospital of Thessaloniki Hippokrateio /ID# 273635
Thessaloniki, 54642
Site Coordinator, +30 2313312672
- Recruiting
Papageorgiou General Hospital /ID# 272735
Thessaloniki, 56429
- Recruiting
General Hospital Of Thessaloniki G. Papanikolaou /ID# 275323
Thessaloniki, 57010
Belgium9 sites, 9 recruiting
- Recruiting
Centre Hospitalier Epicura - Hornu /ID# 273406
Boussu, Hainaut, 7301
- Recruiting
Algemeen Ziekenhuis klina /ID# 273405
Brasschaat, Antwerpen, 2930
- Recruiting
Grand Hôpital De Charleroi - Notre Dame /ID# 273728
Charleroi, Hainaut, 6000
- Recruiting
Ziekenhuis Oost-Limburg, Campus St.-Jan /ID# 273729
Genk, Limburg, 3600
- Recruiting
Universitair Ziekenhuis Brussel /ID# 273403
Jette, Brussels Capital, 1090
- Recruiting
Helora /ID# 273726
La Louvière, Hainaut, 7100
- Recruiting
Groupe Sante CHC - Clinique du MontLegia /ID# 273407
Liège, Liege, 4000
- Recruiting
AZ Oostende /ID# 273714
Ostend, West-Vlaanderen, 8400
- Recruiting
Vitaz /Id# 273408
Sint-Niklaas, Oost-Vlaanderen, 9100
United Kingdom8 sites, 8 recruiting
- Recruiting
NHS Lanarkshire /ID# 276471
Airdrie, North Lanarkshire, ML6 0JS
- Recruiting
Cheltenham General Hospital /ID# 272746
Cheltenham, Gloucestershire, GL53 7AN
- Recruiting
The Christie /ID# 272745
Manchester, M20 4BX
- Recruiting
Milton Keynes Hospital /ID# 272817
Milton Keynes, Buckinghamshire, MK6 5LD
- Recruiting
The Newcastle Upon Tyne Hospitals NHS Foundation Trust /ID# 272748
Newcastle upon Tyne, NE3 3HD
- Recruiting
Nottingham City Hospital /ID# 272753
Nottingham, Nottinghamshire, NG5 1PB
- Recruiting
Queen Alexandra Hospital /ID# 272744
Portsmouth, Hampshire, PO6 3LY
- Recruiting
Royal Cornwall Hospital /ID# 272747
Truro, Cornwall, TR1 3LQ
Argentina6 sites, 6 recruiting
- Recruiting
Hospital Italiano de Buenos Aires /ID# 274418
Buenos Aires, 1181
- Recruiting
Fundacion Argentina contra la Leucemia (FUNDALEU) /ID# 274390
Buenos Aires, 1227
- Recruiting
Hospital Britanico de Buenos Aires /ID# 274419
Ciudad Autonoma de Buenos Aire, Buenos Aires, 1280
- Recruiting
Instituto Alexander Fleming /ID# 277284
Ciudad Autonoma de Buenos Aire, Buenos Aires F.D., 1426
- Recruiting
Hospital Privado Universitario De Córdoba /ID# 274457
Córdoba, Córdoba Province, 5016
- Recruiting
Hospital Universitario Austral /ID# 274393
Pilar, Buenos Aires, 1629
Italy6 sites, 6 recruiting
- Recruiting
I.R.C.C.S Istituto Tumori Giovanni Paolo II /ID# 274217
Bari, 70124
- Recruiting
IRCCS Ospedale San Raffaele /ID# 274789
Milan, Milano, 20132
- Recruiting
Azienda Ospedaliera di Rilievo Nazionale Antonio Cardarelli /ID# 274215
Naples, Napoli, 80131
- Recruiting
Ospedale La Maddalena /ID# 274411
Palermo, 90146
- Recruiting
Azienda Ospedaliera Universitaria Policlinico Tor Vergata /ID# 274572
Rome, Roma, 00133
- Recruiting
A.O.U. CITTA' DELLA SALUTE E DELLA SCIENZA DI TORINO - Ospedale Molinette /ID# 275283
Turin, Piedmont, 10126
Canada5 sites, 5 recruiting
- Recruiting
Cross Cancer Institute /ID# 271504
Edmonton, Alberta, T6G 1Z2
- Recruiting
Health Sciences North /ID# 274738
Greater Sudbury, Ontario, P3E 5J1
- Recruiting
Kingston General Hospital /ID# 272061
Kingston, Ontario, K7L 2V7
- Recruiting
The Moncton Hospital /ID# 277230
Moncton, New Brunswick, E1C 6Z8
- Recruiting
Eastern Health - General Hospital /ID# 272062
St. John's, Newfoundland and Labrador, A1B 3V6
Bulgaria4 sites, 4 recruiting
- Recruiting
University Multiprofile Hospital for Active Treatment Dr. Georgi Stranski /ID# 274893
Pleven, 5800
- Recruiting
Acibadem City Clinic Tokuda University Hospital EAD /ID# 273659
Sofia, 1407
- Recruiting
Specialized Hospital For Active Treatment Of Haematology Diseases /ID# 274955
Sofia, 1756
- Recruiting
Umhat Sveti Ivan Rilsky /ID# 274898
Sofiya, Sofia, 1606
Australia3 sites, 3 recruiting
- Recruiting
Nepean Cancer Centre, Nepean Hospital /ID# 277782
Kingswood, New South Wales, 2747
- Recruiting
Cabrini Hospital Malvern /ID# 277780
Malvern, Victoria, 3144
- Recruiting
Calvary Mater Newcastle /ID# 277783
Waratah, New South Wales, 2298
Israel3 sites, 3 recruiting
- Recruiting
Hadassah Medical Center-Hebrew University /ID# 271616
Jerusalem, 91120
- Recruiting
Rabin Medical Center. /ID# 271614
Petah Tikva, 4941492
- Recruiting
Tel Aviv Sourasky Medical Center /ID# 271615
Tel Aviv, Tel Aviv, 6423906
Austria2 sites, 2 recruiting
- Recruiting
Krankenhaus Der Barmherzigen Brueder Graz /ID# 273288
Graz, Styria, 8020
- Recruiting
Landeskrankenhaus Hochsteiermark, Standort Leoben /ID# 273266
Leoben, Styria, 8700
Mexico2 sites, 2 recruiting
- Recruiting
Hematologica Alta Especialidad /ID# 275279
Huixquilucan de Degollado, 52787
- Recruiting
Centro de Especialidades Hemato-Oncologicas /ID# 275286
Mexico City, 11520
Portugal2 sites, 2 recruiting
- Recruiting
Unidade Local de Saude de Coimbra, EPE /ID# 272720
Coimbra, 3000-075
- Recruiting
Unidade Local de Saúde Trás-os-Montes e Alto Douro /ID# 275404
Vila Real, 5000-185
Site Coordinator, +351259300500
About this study
Official title: EpcoReal: A Multi-country, Prospective Observational Study of Epcoritamab in NHL Comprising Two Patient Cohorts (3L+ (D)LBCL and 3L+ FL)
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.
Read more
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.
- Conditions
- Diffuse Large B-cell Lymphoma, Follicular Lymphoma
- Keywords
- Diffuse large B-cell lymphoma, Follicular Lymphoma, Epcoritamab
- Medical subject headings
- Lymphoma, Large B-Cell, Diffuse, Lymphoma, Follicular
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Epcoritamab | Participants will receive epcoritamab as prescribed by their physician according to local label. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Percentage of Participants Achieving Overall Response (OR)
Defined as the percentage of participants who achieve best overall response of complete response (CR) or partial response (PR) determined by Lugano criteria
Measured: Up to approximately 3 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 Feb 2025
- Study start28 Mar 2025
- Primary completionSep 2031 (estimated)
- Study completionSep 2031 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Diffuse Large B-cell LymphomaStudies of the same condition, open and under way.
- More trials run by AbbVieThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 700 participants (estimated)
Sponsor and investigators
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06830759
- Sponsor's protocol ID
- P24-903
- Acronym
- EpcoReal
- Status last verified
- Feb 2026
- First submitted
- 12 Feb 2025
- Last updated
- 17 Feb 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 17 Feb 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- EpcoReal: A Multi-country, Prospective Observational Study of Epcoritamab in NHL Comprising Two Patient Cohorts (3L+ (D)LBCL and 3L+ FL)
- ClinicalTrials.gov ID
- NCT06830759
- Acronym / sponsor ID
- EpcoReal / P24-903
- Conditions
- Diffuse Large B-cell Lymphoma, Follicular Lymphoma
- Keywords
- Diffuse large B-cell lymphoma, Follicular Lymphoma, Epcoritamab
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 700 participants (estimated)
- Lead sponsor
- AbbVieIndustry (pharma, biotech, devices)
- Collaborators
- Genmab
- Study start
- 28 Mar 2025 (actual)
- Primary completion
- Sep 2031 (estimated)
- Study completion
- Sep 2031 (estimated)
- First posted
- 17 Feb 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Epcoritamab | – | –Participants will receive epcoritamab as prescribed by their physician according to local label. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Adult participants who are being treated with epcoritamab for Diffuse Large B-Cell and Follicular Lymphoma
Key inclusion criteria (3 listed)
- 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.
Key exclusion criteria (2 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Percentage of Participants Achieving Overall Response (OR)
Time frame: Up to approximately 3 years
Defined as the percentage of participants who achieve best overall response of complete response (CR) or partial response (PR) determined by Lugano criteria
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 17 Feb 2026.
- Individual participant dataSharing planned: Undecided
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The CARDIOPROTECT Trial
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
ABBVIE INC. study director
AbbVie
73 sites in 13 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Diffuse Large B-cell Lymphoma and Follicular Lymphoma, run by AbbVie at 73 sites in 13 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 17 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 73 sites in Spain, Greece, Belgium, United Kingdom, Argentina and 8 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Rebekah Taylor ((847) 937-8000, rebekah.taylor@abbvie.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Percentage of Participants Achieving Overall Response (OR) (time frame: Up to approximately 3 years). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Feb 2026.