Phase 1 Leukaemia Trial, Recruiting
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:
- You are 18 years of age or older (any gender)
- You have been diagnosed with a blood cancer that has come back or stopped responding to treatment, specifically B-cell acute lymphoblastic leukaemia (B-ALL), B-cell lymphoma, or multiple myeloma
- You are generally able to carry out daily activities with little to no limitation, and are expected to live for at least 3 more months (confirm with trial site)
- Your blood test results meet certain minimum levels for red blood cells, white blood cells, platelets, and lymphocytes during the screening period (confirm with trial site)
- Your kidneys are working well enough, based on a blood test taken during screening (confirm with trial site)
- Your liver function results are within acceptable ranges during screening (confirm with trial site)
- Your heart is pumping well enough, with no significant fluid around the heart or abnormal heart rhythm readings, based on tests done during screening (confirm with trial site)
- Your blood oxygen level is at least 90% during screening
- If you are a woman who could become pregnant, you must have a negative pregnancy test at screening and not be breastfeeding
- You and your partner (if applicable) must agree to use effective birth control and not donate eggs or sperm from the time you sign the consent form until 1 year after finishing the study treatment
- You, or your legal representative, are willing and able to sign a consent form agreeing to take part in the study
Who may not be able to join:
- You have received chemotherapy, targeted therapy, or immunotherapy recently (within a specific number of days before starting the trial), or radiotherapy within 4 weeks before starting (confirm with trial site for exact timeframes)
- You have had a stem cell transplant (either from a donor or using your own cells) within the 3 months before starting the trial
- You have a history of another type of cancer, unless it was fully treated with no signs of disease for at least 2 years, or it was a type of skin cancer (not melanoma) that has been fully treated with no current signs
- You have previously received a treatment involving a specific type of engineered virus called a VSVG pseudotyped virus (confirm with trial site)
- You have a serious, uncontrolled infection (such as bacterial, viral, or fungal) during the screening period
- You have significant heart problems, such as serious heart failure, a recent heart attack, a recent heart bypass or stent procedure (within 6 months), significant irregular heartbeat, unexplained fainting, or a history of serious heart muscle disease
- You have certain other serious medical conditions, including a primary immune system disorder, a stroke or seizure within the past 6 months, clear signs of dementia or significant mental status changes, or Parkinson's disease or a similar movement disorder
- You have had surgery within 2 weeks before starting the trial, or have surgery planned within 2 weeks after starting (minor procedures done under local anaesthetic may be exempt — confirm with trial site)
- You have received a live vaccine within 1 month before starting the trial
- You have had a severe allergic reaction to this treatment or its ingredients in the past
- A vein cannot be found or accessed easily enough for an intravenous drip
- The trial doctor believes there is another reason why joining the trial would not be suitable for you
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.
Contact this trial
Principal Investigator: Wang Sanbin, MD, 920th Hospital of Joint Logistics Support Force of People's Liberation Army of China
Phone: +86 13187424131
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
Where this trial is recruiting
Primary endpoints
Maximal Tolerated Dose(MTD); Incidence of adverse events(AE) after infusion
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.