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, any gender
- People who have been confirmed by tissue testing to have CD20-positive marginal zone lymphoma (MZL), including MALT, SMZL, or NMZL subtypes
- People whose MZL has come back, gotten worse, or is not suitable for local treatment after having previously received local treatments such as surgery, radiation, Helicobacter pylori treatment, or hepatitis C treatment
- People with a physical fitness/activity level rated 0–2 on a standard scale used by doctors (meaning able to carry out daily activities, even if with some limitations)
- People whose doctor has determined that treatment is needed — for example, due to symptoms, low blood counts, risk of organ damage, large tumour mass, ongoing disease progression, or the person's own wish to be treated
- People whose blood counts and organ function meet specific minimum levels set by the trial (covering blood cell counts, liver function, kidney function, and blood clotting) (confirm with trial site)
- People expected to live at least 3 months or more
- People who are willing to sign a written consent form before the trial begins
Who may not be able to join:
- People who currently have, or have previously been diagnosed with, another cancer — unless they received treatment aimed at a cure and there has been no sign of return or spread in the last 5 years
- People whose lymphoma has spread to the brain or spinal cord, or whose lymphoma has changed into a more aggressive type
- People who have had active bleeding within the 2 months before screening, are currently taking blood-thinning medications, or whose doctor believes they have a clear tendency to bleed
- People who have had major surgery within 6 weeks before screening, or minor surgery within 2 weeks before screening
- People with an active infection, or uncontrolled hepatitis B, hepatitis C, HIV/AIDS, or other serious infectious diseases
- People with a mental health condition or cognitive difficulty that could affect their ability to understand or follow the study requirements
- Women who are pregnant or breastfeeding, or women of childbearing age who are not willing to use contraception during the trial
- People who need to continuously take certain medications that strongly affect how the body processes drugs through a liver enzyme called CYP3A (confirm with trial site which specific medications apply)
- People who the trial doctor considers unsuitable for the trial 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: 15189552696
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
Overall response rate (ORR)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 14 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.