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:
- You are 18 years of age or older
- You have been diagnosed with diffuse large B-cell lymphoma (a type of blood cancer), confirmed by a tissue sample (biopsy)
- You have not received any previous treatment for this cancer, including chemotherapy, targeted therapy, immunotherapy, or radiotherapy
- You have at least one measurable area of cancer that can be tracked during the trial
- Your cancer shows up on a specific type of scan (PET-CT scan), and any affected lymph node is larger than 1.5 cm
- Your cancer is classified as stage II, III, or IV
- You are reasonably functional in daily life — not severely limited by your illness (confirm with trial site)
- You are expected to live for at least 3 more months
- Your blood counts (white blood cells, platelets, and red blood cells) meet certain minimum levels before starting the trial
- Your liver and kidney function tests are within acceptable ranges
- Your blood clotting results are within acceptable ranges
- If you are a woman who could become pregnant, you must have a negative pregnancy test within one week of joining, and agree to use effective contraception from the start of the trial until at least 12 months after your last treatment
- You are willing and able to understand the study requirements and sign a consent form
Who may not be able to join:
- You have a specific subtype of large B-cell lymphoma that started in the brain/spinal cord, testicles, chest (mediastinum), or certain other rare subtypes (confirm with trial site)
- Your lymphoma developed from a previously existing slower-growing (indolent) lymphoma
- Your cancer is currently active in your brain or spinal cord
- You have previously had a stem cell transplant
- You have received any prior treatment for lymphoma, except for short-term or low-dose steroid use
- You have taken any cancer-related herbal medicines or traditional Chinese medicines within the 14 days before starting the trial
- You have a known allergy or sensitivity to the study drug or similar medications
- You are currently taking part in another interventional clinical trial within 4 weeks of starting this trial
- You currently have an active bacterial or viral infection requiring strong or intravenous (IV) medication
- You have a history of immune system deficiency, including HIV
- You have active hepatitis B or hepatitis C infection
- You currently have a syphilis infection
- You have a serious underlying health condition, or alcohol or drug dependency, that could interfere with the trial or make it hard to follow the treatment plan
- You have lung disease (interstitial lung disease) that currently requires treatment
- You have a history of serious heart problems, including dangerous heart rhythm problems, a heart condition affecting the electrical signals of the heart, heart attack, heart failure, stroke, or uncontrolled high blood pressure within the past 6 months (confirm details with trial site)
- You have had another type of cancer within the past 2 years, unless it was a localised cancer that has been fully cured (such as certain skin cancers or early cervical cancer)
- You have a psychological or mental health condition that may make it difficult to follow the trial schedule
- You are currently pregnant or breastfeeding
- The trial doctor considers you 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
Principal Investigator: Lugui Qiu, Professor, Institute of Hematology & Blood Diseases Hospital, China
Phone: +86-022-23608461
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 I:Maximum tolerated dose (MTD); Phase I: Recommended phaseII dose (RP2D); Phase II:Complete remission rate (CRR); Phase I: Dose limited toxicities (DLTs)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 22 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.