Phase 2 Leukaemia Trial, Recruiting NCT06006403 Sponsor: Chongqing Precision Biotech Co., Ltd Condition: Leukaemia
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Phase 2 Leukaemia Trial, Recruiting

NCT06006403
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 old (any gender)
  • People whose cancer cells have tested positive for a protein called CD123, detected through a blood/cell flow test
  • People diagnosed with either relapsed/refractory AML (a type of blood cancer that has come back or stopped responding to treatment) or BPDCN (a rare blood cancer) that is CD123 positive, meeting specific disease criteria (confirm with trial site for exact details)
  • People expected to live for more than 12 weeks
  • People who are reasonably functional day-to-day, rated 0–2 on a standard medical scale called the ECOG scale (meaning able to carry out at least some daily activities)
  • People without serious mental health disorders
  • People whose heart is working well, with a heart pumping strength of at least 50% on an echo scan and no major abnormalities on a heart tracing (ECG)
  • People whose kidneys are functioning within an acceptable range (confirm with trial site)
  • People whose liver is functioning within an acceptable range (confirm with trial site)
  • People with blood oxygen levels above 92%
  • People (or their legal guardian) who are willing to sign a consent form confirming they understand and agree to take part in the study

Who may not be able to join:

  • People who received chemotherapy, targeted therapy, or another experimental treatment within the past 14 days (or within 5 half-lives of the drug, whichever is shorter), unless disease worsening has been confirmed during that treatment
  • People who had a stroke or seizure within the 6 months before signing the consent form
  • People with an active or uncontrolled infection requiring ongoing treatment within 1 week before the screening visit
  • People with moderate to severe heart failure (classified as NYHA Stage III or IV)
  • People who had a heart attack or certain heart surgery within 6 months before joining
  • People with a significant history of irregular heart rhythms or unexplained fainting (not caused by dehydration or a common fainting reflex)
  • People with a history of severe non-ischemic heart muscle disease
  • People with active hepatitis B infection
  • People with active autoimmune disease who require long-term immune-suppressing medication
  • People with another active cancer, except for certain fully treated early-stage cancers (such as some skin cancers, early cervical cancer, localised prostate cancer, or early breast cancer after surgery — confirm with trial site)
  • People who received a live attenuated vaccine within 4 weeks before screening
  • Women who are pregnant or breastfeeding
  • People of any gender who plan to have children within 1 year of receiving the CAR T cell treatment used in this trial
  • People who the research team considers unsuitable for other reasons

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
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: Jia Wei, M.D, Shanxi Bethune Hospital

Phone: 13986102084

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
Chongqing Precision Biotech Co., Ltd
Registry
ClinicalTrials.gov
Start date
31 August 2023
Est. completion
31 December 2025

Where this trial is recruiting

🇨🇳 China

Primary endpoints

To evaluate the safety of CAR-NK cell preparations in the treatment of Relapsed/Refractory Acute Myeloid Leukemia or Blastic Plasmacytoid Dendritic Cell Neoplasm[Safety and Tolerability]; To evaluate the efficacy of CAR-NK cell preparations in the treatment of Relapsed/Refractory Acute Myeloid Leukemia or Blastic Plasmacytoid Dendritic Cell Neoplasm[Effectiveness]

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