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:
- People who have been diagnosed with extranodal NK/T-cell lymphoma (a type of lymphoma), confirmed through tissue and laboratory testing using standard diagnostic criteria.
- People whose lymphoma has come back after initially responding to treatment, has not responded to treatment, or has been newly diagnosed at an advanced stage (stage III or IV).
- People who have at least one area of disease that can be measured and tracked on a PET/CT scan, CT scan, or MRI.
- People who are expected to live for more than 3 months.
- People who are in reasonably good general health, as measured by a standard medical scoring system (ECOG score of 0–2, meaning able to carry out at least some daily activities).
- People whose recent blood test results (taken within 1 week before joining) show that blood cell counts, kidney function, liver function, and a blood protein called fibrinogen are all within the acceptable ranges set by the trial.
- People who have signed a form agreeing to take part in the trial.
Who may not be able to join:
- People whose lymphoma has spread to the brain or spinal cord, or who have another type of cancer.
- People who have previously received a type of medication called a PI3K inhibitor.
- People whose general health is too poor (ECOG score of 2 or higher) (confirm with trial site, as this overlaps with an inclusion criterion).
- People who are pregnant or breastfeeding.
- People who could potentially have children but are unwilling or unable to use effective contraception during the trial.
- People who are allergic to any of the medications used in the trial.
- People who currently have an active infection.
- People with a history of immune system deficiency, including HIV, other inherited or acquired immune conditions, or a history of organ transplant.
- People with a history of a lung condition called interstitial pneumonia, or non-infectious pneumonia, or where this condition is strongly suspected.
- People with a past history of neurological or psychiatric conditions, including epilepsy or dementia.
- People who, in the treating doctor's judgment, have other health conditions that could seriously affect their safety or their ability to complete 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: Liang Wang, M.D., Beijing Tongren Hospital
Phone: +861058268442
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
The best objective response rate(ORR) over 6 treatment cycles
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.