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 to 75 years old (inclusive)
- People who have been diagnosed with a type of B-cell non-Hodgkin lymphoma (a blood cancer) that has been confirmed by laboratory testing to carry a marker called CD19
- People whose lymphoma has come back or stopped responding to treatment — either after at least 2 previous treatments for any B-cell lymphoma type, or after failing first-line treatment for certain aggressive types, or after a stem cell transplant using their own cells (confirm specific disease history with trial site)
- People whose doctors estimate they have more than 3 months to live
- People who are well enough to carry out basic daily activities, based on a standard medical fitness scale (ECOG score of 0–2)
- People who have at least one measurable area of lymphoma visible on a CT or MRI scan, meeting specific size requirements
- People who are willing to provide a tissue sample (either a fresh biopsy or preserved tumour tissue slides)
- People whose heart, kidneys, liver, lungs, and blood counts meet minimum function levels as tested before joining (confirm specific values with trial site)
- Women of childbearing age whose pregnancy test comes back negative, and all participants who agree to use effective contraception during treatment and for 1 year afterward
- People whose side effects from previous cancer treatments have largely resolved to mild or acceptable levels
- People with no significant inherited genetic conditions
- People who are willing and able to understand and follow the trial requirements, and who sign informed consent
Who may not be able to join:
- People who have lymphoma that has spread to the brain or spinal cord, or who have a significant history of neurological conditions such as epilepsy or stroke-related disease
- Women who are pregnant or breastfeeding, or anyone unwilling to use effective contraception during treatment and for 1 year afterward
- People who have previously had a stem cell transplant using donor cells, or an organ transplant
- People with another active cancer that is not currently in remission
- People with a primary immune deficiency or an autoimmune condition that requires immune-suppressing medication
- People who received radiation therapy within 3 months before joining
- People who received certain immunotherapy drugs (such as PD-1, PD-L1, or CD19/CD3 bispecific antibodies) within 4 weeks before joining
- People who received any immune cell-based therapy within 6 months before joining
- People whose blood tests show a positive reaction to a specific component used in the trial's cell treatment (anti-CD19 scFv)
- People who have participated in another clinical trial within 4 weeks before joining
- People with uncontrolled infections or serious illnesses, including HIV, active hepatitis B or C, heart failure, unstable chest pain, or irregular heartbeat
- People with large uncontrolled fluid build-up around the lungs or in the abdomen
- People who have had a stroke or bleeding in the brain within 3 months before joining
- People who have had major surgery or a serious injury within 28 days before joining, or who have not yet recovered from its effects
- People who received donated immune cells (such as donor lymphocyte infusion) within 6 weeks before joining
- People with a known allergy to any ingredient in the trial's cell treatment
- People with a mental or physical condition that, in the treating doctor's opinion, would prevent safe or meaningful participation in the trial
- People who are unable or unwilling to understand and sign the informed consent form
- People considered unsuitable by the trial investigators for any other reason
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
Phone: +86-010-55499341
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
Phase 1: Incidence of Adverse Events (AEs); Phase 1: Incidence of Dose-Limiting Toxicities (DLTs); Phase 1: Recommended phase 2 dose (RP2D); Phase 2: Best objective Response Rate
Can't join this trial?
Data last synced from ClinicalTrials.gov: 16 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.