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:
- Adults aged 18 or older, of any gender
- People with a laboratory-confirmed diagnosis of CD20-positive follicular lymphoma (a type of slow-growing blood cancer), classified as Grade 1, 2, or 3A under standard medical guidelines
- People with advanced-stage disease (Stage III or IV), or Stage II with a large tumour mass, who also meet at least one of the following: a tumour or lymph node measuring 7 cm or more; symptoms or organ problems caused by growing lymph nodes or tumours; fever, night sweats, or unintentional weight loss of more than 10% of body weight within 6 months; fluid build-up in the chest or abdomen from the lymphoma; low blood counts caused by lymphoma in the bone marrow; three or more lymph nodes each measuring at least 3 cm; or an enlarged spleen causing symptoms
- People who have never received systemic (whole-body) treatment for this type of lymphoma before
- People with a general health and activity level rated at 2 or below on a standard medical scale (meaning able to carry out basic self-care, though possibly not all physical activity)
- People with at least one tumour that is measurable on a scan (larger than 2 cm)
- People with a life expectancy of at least 6 months
- People whose blood counts, liver, and kidney function meet minimum levels required by the trial (confirm with trial site for specific values)
- People who are willing and able to use highly effective contraception during the trial and for 4 weeks after treatment ends (applies to people who could father or become pregnant)
- People who are willing to sign a consent form and take part voluntarily
- People who can provide tumour tissue samples (either previously stored or freshly collected) for laboratory testing
Who may not be able to join:
- People whose lymphoma has spread to the brain or spinal fluid, or whose cancer has changed into a more aggressive type (such as diffuse large B-cell lymphoma)
- People with Grade 3B follicular lymphoma or transformed follicular lymphoma
- People with Stage I follicular lymphoma
- People with a history of another cancer, unless they have been free of that cancer for at least 5 years and their treating doctor considers the risk of it returning to be low (some exceptions may apply for certain skin cancers, early prostate cancer, or specific cervical conditions — confirm with trial site)
- People who have taken an experimental drug, certain antibiotics, or who have participated in another interventional clinical trial within the 4 weeks before enrolling
- People who have had major surgery (other than a lymph node biopsy) within 14 days before enrolling, or who are expected to need major surgery during the trial
- People who have previously been treated with zanubrutinib, obinutuzumab, or lenalidomide
- People with immune system disorders, certain autoimmune diseases, or those who have been taking high-dose steroid or immune-suppressing medications within 7 days before enrolling
- People with severe liver disease, severe malnutrition, or failure of multiple organs including the kidneys
- People with significant heart problems, including severe heart failure, a heart attack within the past 6 months, dangerous heart rhythm problems, uncontrolled high blood pressure, or unstable chest pain
- People with active HIV infection, active hepatitis B or C infection at significant levels, or other uncontrolled serious infections
- People with bleeding disorders, clotting abnormalities, or a blood clot event within the past 3 months
- People with a known severe allergy to any of the ingredients in the study medications
- People who are pregnant, breastfeeding, or unwilling to use effective contraception
- People whom the trial doctors consider unsuitable for other medical reasons
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: Shuhua Yi, Institute of Hematology & Blood Diseases Hospital, China
Phone: +86-022-23909106
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
Objective response rate,ORR
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.