Phase 1 Leukaemia Trial, Recruiting NCT07239323 Sponsor: Chongqing Precision Biotech Co., Ltd Condition: Leukaemia
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Phase 1 Leukaemia Trial, Recruiting

NCT07239323
Recruiting Phase 1

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.

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 28 July 2026
Phase 1: approximately ~10% 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: 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

Status
Recruiting
Phase
Phase 1
Sponsor
Chongqing Precision Biotech Co., Ltd
Registry
ClinicalTrials.gov
Start date
1 July 2025
Est. completion
31 December 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Maximal Tolerated Dose(MTD); Incidence of adverse events(AE) after infusion

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: 28 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