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 who have been diagnosed with a specific type of blood cancer called diffuse large B-cell lymphoma, confirmed by laboratory testing of tissue samples, where the cancer cells test positive for a protein called CD20.
- People whose lymphoma has been confirmed by a pathologist to be a "double-expressor" type, meaning the cancer cells show high levels of two specific proteins (MYC at 40% or above, and BCL2 at 50% or above).
- People whose cancer showed a complete response (no detectable cancer) after their first course of treatment.
- People aged 18 to 80 years.
- People whose general physical health and ability to carry out daily activities falls within a certain range, as assessed using a standard medical scale (confirm with trial site).
- People with no history of any other cancer, either in the past or currently.
- People whose lymphoma is rated above a score of 1 on a standard risk-assessment tool called the International Prognostic Index (confirm with trial site).
- People who test positive for a specific marker in the blood called ctDNA MRD at the time of enrolling in the trial, which indicates a small amount of cancer-related material may still be present.
- People expected to live for at least 6 months, based on the treating doctor's assessment.
- People who provide written consent before any trial procedures begin.
Who may not be able to join:
- People whose cancer did not achieve a complete response after their first course of treatment.
- People who have previously had an organ transplant.
- People with uncontrolled blood clotting problems or active bleeding.
- People with uncontrolled heart or blood vessel disease, including reduced heart pumping function (below 50%), certain connective tissue conditions, or serious active infections.
- People who had major surgery within 6 weeks before joining the trial.
- People whose routine blood test results — for reasons unrelated to their lymphoma — fall outside acceptable ranges, including low white blood cell counts, low platelet counts, or abnormal liver or kidney function levels (confirm with trial site for specific thresholds).
- People with active hepatitis B infection that does not meet specific virus level requirements set by the trial (people who test positive for certain hepatitis B markers will need additional testing to determine whether they meet the trial's requirements).
- People with HIV infection.
- People currently receiving any cancer treatment for lymphoma or another cancer.
- People with drug or alcohol dependence that may affect how trial results are assessed.
- People with a psychiatric illness or any condition that would make it difficult to follow the trial's requirements.
- People who need to take certain medications that strongly affect how the body processes drugs (called CYP3A inhibitors or inducers), or who have taken these medications within 7 days — or within a set number of half-lives — before the first trial dose (confirm with trial site).
- People who cannot swallow capsules, or who have significant digestive system conditions that may affect how the body absorbs medication, such as malabsorption conditions, previous weight-loss surgery, inflammatory bowel disease, or bowel blockage.
- People with any other serious uncontrolled medical condition that the trial doctor believes could affect safety, drug absorption, or place the person at unacceptable risk.
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: Rong Tao, MD & PhD, Fudan University
Phone: 008621-64175590
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
ctDNA MRD Negativity Rate; 2-Year Progression-Free Survival Rate
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.