Lymphoma Trial, Recruiting NCT07072221 Sponsor: The First Affiliated Hospital of Soochow University Condition: Lymphoma
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Lymphoma Trial, Recruiting

NCT07072221
Recruiting Not Applicable

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 or older, of any gender
  • People who are able to understand the study and are willing to sign a written consent form
  • People with a performance status score of 0–3 on the ECOG scale, which measures how much a condition affects daily activity (confirm with trial site)
  • People whose doctors expect them to live for more than 3 months
  • People who have been diagnosed with peripheral T-cell lymphoma (PTCL) confirmed by tissue or cell testing, using the 2022 World Health Organization classification system
  • People who have at least one measurable area of lymphoma that is large enough to be detected on a PET/CT scan (short diameter of 15mm or more)
  • People whose PTCL has come back or stopped responding to treatment, who have already been through at least one previous treatment, and who have never been treated with the drugs chidamide, lenalidomide, or bendamustine
  • People whose side effects from previous treatments have mostly resolved — all non-hair-loss side effects must have settled to a mild level (Grade 1 or lower) before joining
  • People whose heart, liver, kidneys, and lungs are functioning at an adequate level as measured by specific tests (confirm with trial site for exact values)
  • People whose bone marrow is producing enough blood cells, based on blood test results meeting specific minimum levels (confirm with trial site for exact values)
  • People who are willing to use contraception throughout the study and follow-up period if there is any possibility of pregnancy
  • People who are likely to follow the study plan and attend all required visits

Who may not be able to join:

  • People whose lymphoma has returned or stopped responding to treatment and who have previously been treated with chidamide, lenalidomide, or bendamustine, or who have had any other cancer treatment within the past 4 weeks
  • People who have been enrolled in another clinical trial within the past 4 weeks
  • People who have HIV infection, or active hepatitis B or C
  • People who have an active infection that is not under control
  • People with severe liver or kidney problems, based on specific blood test results (confirm with trial site)
  • People who have a serious heart condition or severe irregular heartbeat that is causing symptoms or affecting heart function
  • People who have another cancer that currently needs treatment
  • People who have a history of blood clots in their veins or arteries, either in the past or currently
  • People who are pregnant or breastfeeding
  • People who have severely weakened immune systems
  • People with psychological conditions that would make it difficult to participate in the study or sign a consent form
  • People who are unlikely to be able to complete all required study visits and procedures

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 12 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: 67781856

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
Not Applicable
Sponsor
The First Affiliated Hospital of Soochow University
Registry
ClinicalTrials.gov
Start date
1 November 2024
Est. completion
1 August 2029

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Complete response rate(CRR)

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: 12 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