Phase 2 Lymphoma Trial, Recruiting NCT07058103 Sponsor: The Affiliated Hospital of Xuzhou Medical University Condition: Lymphoma
Back to Lymphoma

Phase 2 Lymphoma Trial, Recruiting

NCT07058103
Recruiting Phase 2

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 8 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

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

Status
Recruiting
Phase
Phase 2
Sponsor
The Affiliated Hospital of Xuzhou Medical University
Registry
ClinicalTrials.gov
Start date
1 April 2025
Est. completion
1 April 2028

Where this trial is recruiting

🇨🇳 China

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?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov