Phase 2 Leukaemia Trial, Recruiting NCT07584889 Sponsor: Shenzhen University General Hospital Condition: Leukaemia
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Phase 2 Leukaemia Trial, Recruiting

NCT07584889
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 aged 18 to 75 years, of any gender
  • People who have been diagnosed with a blood cancer that is CD19-positive (a specific protein found on cancer cells) and has come back or stopped responding to treatment, confirmed by laboratory testing under 2022 World Health Organization guidelines
  • People with a general health and activity level rated as reasonably functional (a standard medical score of 0, 1, or 2 on a scale used by doctors to measure how much a condition affects daily activities)
  • People with a life expectancy of at least 3 months
  • People who have no medical reasons preventing a procedure to collect white blood cells from the blood (called leukapheresis)
  • People whose cancer cells have been confirmed to carry the CD19 protein, shown through specific laboratory tests
  • People without serious problems affecting the heart, lungs, liver, or kidneys
  • People who are able to understand the study and are willing to sign a consent form

Who may not be able to join:

  • People with a known allergy to any ingredient in the cell-based treatment being studied
  • People whose blood test results show that certain blood cell counts are too low (white blood cells, neutrophils, lymphocytes, or platelets are below specific levels)
  • People whose blood tests show the liver or kidneys are not working well enough, based on specific chemical levels in the blood
  • People with significant heart failure classified at a severe level, or whose heart pumping function is below 50% as measured by an ultrasound of the heart
  • People whose lungs are not working well enough, shown by blood oxygen levels below 92% while breathing normal room air
  • People who have had a heart attack, heart procedure, unstable chest pain, or another serious heart condition within the 12 months before joining
  • People with severely high blood pressure that has not been brought under control despite taking medication
  • People with a history of brain injury, loss of consciousness, epilepsy (seizures), serious lack of blood supply to the brain, or bleeding in the brain
  • People with an autoimmune disease, a weakened immune system, or any condition that requires ongoing treatment with medicines that suppress the immune system
  • People with an active infection that is not under control
  • People who have previously received CAR-T cell therapy or any other treatment involving genetically modified T-cells
  • People who have received a live vaccine within 4 weeks before joining the trial
  • People who test positive for HIV, hepatitis B, hepatitis C, or syphilis, or who are carriers of hepatitis B
  • People with a history of alcohol misuse, drug misuse, or a psychiatric illness
  • People who have taken part in another clinical trial within 3 months before joining this study
  • Women who are pregnant or breastfeeding, planning to become pregnant during the study, or who are able to become pregnant and are unwilling or unable to use effective contraception
  • People who, in the opinion of the trial doctor, have any other condition that makes participation unsuitable (confirm with trial site)

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 14 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

Principal Investigator: lixin wang, PHD, Shenzhen University General Hospital

Phone: 0755-21839999

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
Shenzhen University General Hospital
Registry
ClinicalTrials.gov
Start date
20 April 2024
Est. completion
19 April 2029

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: 14 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