Phase 2 Lymphoma Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People aged 18 or older at the time of giving consent to join the trial
- People who have been diagnosed with a type of B-cell non-Hodgkin's lymphoma (a blood cancer) that has been confirmed by a tissue test
- People whose organs (such as kidneys, liver, and heart) are functioning well enough to meet the trial's requirements
- People whose lymphoma has come back or stopped responding to treatment, in one of the following ways: after at least 2 rounds of treatment (or at least 1 round for certain specific lymphoma types including Burkitt lymphoma, Precursor B-cell lymphoblastic lymphoma, or Mantle cell lymphoma); or the cancer came back or got worse within 12 months of a stem cell transplant using the patient's own cells; or for people who cannot have a stem cell transplant, the cancer did not respond well enough to earlier lines of treatment (confirm with trial site for full details)
- People who have previously received a specific combination of treatments that included both an anti-CD20 antibody therapy (a type of targeted drug) and a chemotherapy regimen containing a drug called an anthracycline
- People whose lymphoma shows up as active on a PET scan (a type of imaging test) based on specific 2014 guidelines
- People who are well enough to carry out basic daily activities, based on a standard health performance scale (scored 0, 1, or 2 out of 5)
- People whose side effects from previous treatments have mostly settled, with symptoms at a mild level (Grade 1 or lower)
Who may not be able to join:
- People who have previously received a cell-based therapy that targeted a protein called CD19
- People with a history of a condition called Richter's transformation, which is a change from a type of blood cancer called chronic lymphocytic leukaemia
- People who have had another separate cancer that has not been in remission for at least 2 years
- People with a history of, or currently living with, a significant condition affecting the brain or spinal cord
- People whose lymphoma has spread to the brain or spinal cord and is getting worse, or where a mass in the brain may soon cause symptoms
- People who have lymphoma actively involving the heart that is not responding to treatment
- People who have had a heart attack, a procedure to open blocked heart arteries, a heart stent placed, unstable chest pain, or another serious heart condition within the past 6 months
- People with an active, uncontrolled infection caused by bacteria, fungi, or a virus (note: people with HIV, hepatitis B, or hepatitis C may still be considered eligible if their infection is being treated and the virus is under control — confirm with trial site)
- People with a history of an autoimmune disease (where the immune system attacks the body) that caused organ damage or required ongoing immune-suppressing medication within the last 2 years
- People who have had a serious allergic reaction to any of the medicines used in this trial, including the preparatory chemotherapy drugs
- People with a blood clot in a vein or a clot that has travelled to the lungs, if it is not being managed on a stable blood-thinning treatment
- People who have had a stem cell transplant using their own cells within the 3 months before giving consent to join the trial
- People who have had a stem cell transplant using someone else's cells, if they are experiencing a complication called graft-versus-host disease that still requires treatment with steroids or other specific medications within the past 12 weeks
- People who have received a live vaccine within 3 months before the planned start of the preparatory treatment for the trial
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Pei Wang, PhD, Eureka Therapeutics Inc.
Phone: 925-949-9314
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
To assess the Dose Limiting Toxicities of EB103.; Incidence rates of Treatment-Emergent Adverse Events of EB103.; Incidence rates Treatment-Emergent Laboratory Abnormalities reported for EB103.; To determine the Recommended Phase II Dose (RP2D) of EB103.
Can't join this trial?
Data last synced from ClinicalTrials.gov: 6 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.