Leukaemia Trial, Recruiting NCT06232694 Sponsor: The First Affiliated Hospital with Nanjing Medical University Condition: Leukaemia
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Leukaemia Trial, Recruiting

NCT06232694
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:

  • People who have been newly diagnosed with acute myeloid leukemia (AML), based on the 2022 WHO diagnostic guidelines.
  • People aged between 18 and 60 years old.
  • People who are reasonably active and able to care for themselves, with only mild or no limitations on daily activities (as measured by a standard medical scoring tool called the ECOG scale, scores 0–2).
  • People whose heart is pumping adequately, as shown by a heart ultrasound result of 45% or higher.
  • People whose kidneys are working well enough, based on a specific calculation or urine test showing sufficient kidney filtration capacity.
  • People whose liver is functioning within acceptable limits, based on blood test results for liver enzymes and bilirubin (unless any abnormal results are caused by the leukemia itself).
  • People who have read, understood, and signed a consent form agreeing to take part in the trial.

Who may not be able to join:

  • People whose AML is a specific subtype called acute promyelocytic leukemia (APL).
  • People whose AML has returned after treatment or has not responded to previous treatment.
  • People whose leukemia is known to have spread to the brain or spinal cord.
  • People known to be living with HIV, due to potential interactions between HIV medications and one of the trial drugs (confirm with trial site regarding HIV testing requirements).
  • People with active hepatitis B or hepatitis C infections — though inactive carriers, or those with very low virus levels who are receiving permitted antiviral treatment, may not be automatically excluded (confirm with trial site).
  • People who have taken certain medications that strongly affect how the body processes drugs (known as strong or moderate CYP3A inducers or inhibitors) within the 7 days before starting the trial treatment.
  • People with significant heart disease that causes symptoms such as tiredness, breathlessness, or chest pain even with ordinary everyday activity, or with more severe heart conditions.
  • People who need continuous oxygen therapy to manage a long-term breathing condition.
  • People who are unable to swallow tablets or capsules, or whose body cannot properly absorb medications taken by mouth.
  • People who have an active infection (bacterial, viral, or fungal) that is not under control.
  • People who have previously been treated with the drug venetoclax, or who are currently taking part in another clinical trial involving an experimental drug.

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
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

Phone: +8613914722662

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

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Trial details

Status
Recruiting
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
1 January 2024
Est. completion
30 December 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

The composite complete remission rate (CR+CRi)

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