Leukaemia Trial, Recruiting NCT05620680 Sponsor: Shenzhen University General Hospital Condition: Leukaemia
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Leukaemia Trial, Recruiting

NCT05620680
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 between 18 and 75 years old, any gender
  • People who are willing to take part and have signed a consent form (either themselves or through a legal guardian)
  • People who have been diagnosed with T-cell lymphoma according to specific recognised medical guidelines
  • People whose T-cell lymphoma has come back after treatment or has not responded to treatment — meaning either the cancer did not go into full remission after initial treatment, or it returned with signs of disease in the blood, bone marrow, or other areas of the body
  • People who have not received antibody-based therapy in the 2 weeks before the cell therapy is given
  • People who are reasonably active and able to carry out daily activities (measured by a standard medical scoring system called ECOG, with a score of 0 to 2)
  • People who are able to undergo a blood-filtering procedure called apheresis, which collects cells from the blood
  • People who are expected to live for more than 3 months

Who may not be able to join:

  • People who have had an allergic reaction to any ingredient used in the cell therapy product
  • People whose blood test results show certain concerning levels, including high bilirubin, high liver enzyme levels (ALT or AST), high creatinine, or very low platelet counts
  • People with significant heart failure classified as class III or IV, or whose heart pumping function (measured by an ultrasound of the heart) is below 50%
  • People with poor lung function or blood oxygen levels below 92% while breathing normal room air
  • People who have had a heart attack, heart procedure (such as angioplasty or stenting), unstable chest pain, or another serious heart condition within the past 12 months
  • People with severe high blood pressure that cannot be controlled with medication
  • People who currently have another advanced cancer (though people whose other cancer has been treated and is considered stable may still be considered)
  • People with a history of serious head injury, loss of consciousness, epilepsy, or significant stroke or brain bleeding
  • People with active leukemia affecting the central nervous system (brain and spinal cord) that is resistant to certain treatments, or who are currently receiving radiation to the head or spine (those with a previous history that has been successfully treated may still be considered — confirm with trial site)
  • People with autoimmune diseases, immune system disorders, or those who need medications that suppress the immune system
  • People who currently have an active, uncontrolled infection
  • People who have previously received any CAR-T cell therapy or other genetically modified T cell therapy
  • People who have received a live vaccine within 4 weeks before joining the trial
  • People with HIV, hepatitis B (HBV), hepatitis C (HCV), or syphilis infections, including those who carry hepatitis B without symptoms
  • People with a history of alcohol dependence, drug addiction, or mental illness
  • People who have taken part in another clinical trial within the 3 months before joining this study
  • Women who are pregnant or breastfeeding, who plan to become pregnant during the trial, or who are able to become pregnant but are unable to use effective contraception
  • People whom the trial doctors consider unsuitable for the study 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 22 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

Principal Investigator: Li Yu, Dr, Shenzhen University General Hospital

Phone: +8675521839178

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
Shenzhen University General Hospital
Registry
ClinicalTrials.gov
Start date
1 October 2022
Est. completion
31 October 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

TEAEs

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: 22 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