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 Angioimmunoblastic T-cell lymphoma (AITL) according to the 2016 WHO classification, and who have at least one measurable area of disease (a lymph node larger than 1.5 cm, or a non-lymph node affected area larger than 1.0 cm).
- People whose AITL has come back or stopped responding after at least one previous treatment, such as chemotherapy or a stem cell transplant.
- People aged 18 or older, of any sex, who are well enough to carry out some daily activities (confirm with trial site regarding the specific fitness scale used).
- People who are expected to live for more than 3 months.
- People who are willing and able to attend follow-up appointments and understand what taking part in the study involves.
Who may not be able to join:
- People with significantly abnormal liver or kidney function test results (more than twice the normal range), unless the trial site considers this to be caused directly by the lymphoma.
- People whose blood counts are too low — specifically, low white blood cells, low platelets, or low haemoglobin — unless the trial site considers this to be caused by lymphoma affecting the bone marrow.
- People who have previously received certain treatments, including: the chemotherapy drug mitoxantrone (or its liposome form); PD-1 or PD-L1 immunotherapy drugs; or a type of drug called a histone deacetylase inhibitor for this condition.
- People with serious heart problems, including severe heart failure, a weakened pumping function of the heart (ejection fraction below 50%), or certain heart conditions within the past 6 months such as a heart attack, severe heart failure, or problems with heart rhythm (confirm with trial site for full details).
- People who have HIV/AIDS, active syphilis, active hepatitis B (with viral levels above a certain threshold), or hepatitis C.
- People who have another cancer that is not well controlled, or another blood disorder such as haemophilia or myelofibrosis, where the trial doctor considers participation unsuitable.
- People with a history of autoimmune disease who are currently taking immune-suppressing medications above a certain dose or for more than two weeks before joining.
- People with an active infection (bacterial, fungal, or viral) that is not responding to treatment.
- People with an uncontrolled condition called haemophagocytic syndrome (a serious immune system disorder).
- People who have had major surgery within 3 weeks before starting treatment.
- People who have taken part in, or are currently participating in, another clinical drug trial within the 30 days before joining.
- Women who are pregnant or breastfeeding, or people of childbearing age who are not willing to use contraception.
- People with a known allergy to any component of the study drug.
- People whom the trial doctor considers unsuitable for enrolment 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
Phone: +86136452076
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
To evaluate the Objective Response Rate (Complete response+Partial response) of tirelizumab in combination with cyclophosphamide, mitoxantrone liposomes, sidaraniline, and prednisone in subjects with relapsed/refractory angioimmunoblastic T-cell lymphoma
Can't join this trial?
Data last synced from ClinicalTrials.gov: 8 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.