Phase 2 Leukaemia 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 to 75 years old
- People who have been diagnosed with a type of blood cancer called CLL (Chronic Lymphocytic Leukaemia) or SLL (Small Lymphocytic Lymphoma), confirmed using standard diagnostic guidelines
- People who have not previously received treatment for CLL/SLL — those who received only brief, limited prior treatment may still be considered, provided it did not include certain chemotherapy combinations (such as CHOP or COP), fludarabine, bendamustine, or ibrutinib; chlorambucil or cyclophosphamide was given for less than 3 weeks; interferon was given for less than 6 months; and no meaningful response to that prior treatment was seen (confirm with trial site)
- People whose CLL/SLL now needs treatment, shown by at least one of the following signs: a drop in red blood cell levels, a drop in platelet levels, an enlarged spleen, significantly enlarged lymph nodes, a rapid rise in white blood cell counts, involvement of organs outside the lymph nodes (such as skin or kidneys), or symptoms such as unintentional weight loss of 10% or more in the past 6 months or severe fatigue affecting daily life
- People who are reasonably active and able to care for themselves, as measured by a standard health performance scale (score of 0 to 2 out of 4)
- People who are expected to survive for at least 3 months
Who may not be able to join:
- People who have had another type of cancer (other than CLL) within the past year, including lymphoma affecting the brain or spinal cord
- People whose CLL/SLL has transformed into a more aggressive form of lymphoma or progressed to a related condition called prolymphocytic leukaemia
- People who have active autoimmune conditions causing the immune system to attack their own red blood cells or platelets, and who require treatment for those conditions
- People with liver or kidney function that falls below the levels required for the trial, as shown by blood test results (confirm with trial site for specific values)
- People with a severe or uncontrolled infection
- People with a condition affecting the nervous system that is causing noticeable symptoms
- People with other serious health conditions that the trial doctor considers may affect the study, such as uncontrolled diabetes, stomach ulcers, or significant heart or lung disease
- People with ongoing, uncontrolled bleeding
- People who have had a serious, life-threatening bleeding episode in the past, particularly from a cause that cannot be corrected
- People who need to take blood-thinning (anticoagulant) medication continuously
- People who have had major surgery within the 30 days before joining (lymph node biopsy is not included in this restriction)
- Women who are pregnant or breastfeeding, or women of childbearing age who are unwilling to use contraception during the trial
- People with a known allergy to any medication used in the trial
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: Zengjun Li, Institute of Hematology & Blood Diseases Hospital Chinese Academy of Medical Sciences & Peking Union Medical College
Phone: +86 13642138692
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
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Trial details
Where this trial is recruiting
Primary endpoints
CRR
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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.