Phase 2 Lymphoma Trial, Recruiting NCT07168317 Sponsor: The Affiliated Hospital of Xuzhou Medical University Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT07168317
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) based on standard medical classification guidelines, and who have at least one area of disease that can be measured on scans (a swollen lymph node larger than 1.5 cm, or a growth outside the lymph nodes larger than 1.0 cm)
  • People who have never received any previous treatment for this condition, including chemotherapy or radiation
  • People aged 18 or older, of any gender, who are reasonably functional in daily life (confirm with trial site regarding the specific activity level 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 abnormal liver or kidney function test results more than twice the normal level, unless the trial site determines those results are caused by the lymphoma itself
  • People whose bone marrow is not producing enough blood cells (low white blood cells, low platelets, or low haemoglobin), unless the trial site determines this is caused by the lymphoma affecting the bone marrow
  • People who have previously had any local or systemic cancer treatment
  • People with significant heart problems, including severe heart failure, a weakened pumping function of the heart, or certain heart conditions (such as heart attack, serious irregular heartbeat, or a history of abnormal heart rhythm) occurring within the past 6 months
  • People with HIV/AIDS, syphilis, active hepatitis B, or hepatitis C
  • People who have another cancer that is not well controlled, or another blood disorder such as haemophilia or myelofibrosis, where the treating doctor considers enrolment unsuitable
  • People with a history of autoimmune disease, or who are currently taking immune-suppressing medication above a certain dose or for more than 2 weeks (confirm with trial site for specific details)
  • People with an active infection that is not responding to treatment
  • People with an uncontrolled condition called haemophagocytic syndrome, where the immune system attacks the body's own cells
  • People who have had a significant surgical procedure within 3 weeks before starting treatment
  • People who have taken part in another clinical drug trial within the past 30 days, or who are currently enrolled in another trial of a new drug
  • People who are pregnant, breastfeeding, or of childbearing age and unwilling to use contraception during the trial
  • People who are known to be allergic to any ingredients in the trial medication
  • People whom the treating 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 6 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: 136452076

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 August 2025
Est. completion
1 August 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Outcome Measure

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: 6 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