Phase 2 Leukaemia Trial, Recruiting NCT07023588 Sponsor: Yehui Tan Condition: Leukaemia
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Phase 2 Leukaemia Trial, Recruiting

NCT07023588
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 who have been newly diagnosed with acute myeloid leukaemia (AML), confirmed through bone marrow testing.
  • People who have completed a full set of specialised leukaemia tests covering the appearance of cells, cell markers, chromosomes, and gene changes.
  • People aged 18 years or older.
  • People whose general physical fitness and ability to carry out daily activities falls within an acceptable range, as assessed using a standard medical scale (ECOG score of 0–2).
  • People whose blood test on day 6 of treatment shows at least 1% leukaemia blast cells circulating in the blood (confirm with trial site).
  • People whose kidneys are functioning well enough to meet a specific minimum level, measured by a standard calculation or urine test.
  • People whose liver is functioning within acceptable limits based on blood test results, unless any abnormality is considered to be caused by the leukaemia itself.
  • People whom the treating doctor considers suitable to receive a specific chemotherapy regimen used in this trial (DA or IA therapy).
  • People who have read, understood, and signed the informed consent form for the trial.

Who may not be able to join:

  • People whose AML is the specific subtype known as acute promyelocytic leukaemia (APL).
  • People diagnosed with a mixed-type acute leukaemia (MPAL), where the leukaemia cells show features of more than one blood cell type.
  • People whose AML has spread to the brain or spinal cord.
  • People whose AML has spread to areas outside the bone marrow, forming disease in other parts of the body.
  • People with significantly reduced kidney or liver function beyond the limits described in the eligibility requirements.
  • People with serious heart conditions, such as heart failure, a recent heart attack, or significant problems with how the heart functions.
  • People who currently have another active cancer in another part of the body (people with a history of a cancer that has been fully cured may still be considered eligible — confirm with trial site).
  • People with active tuberculosis, or people who are HIV-positive.
  • People who have another blood or bone marrow disorder at the same time.
  • People who are pregnant or currently breastfeeding.
  • People who are unable to understand or follow the requirements of the study.
  • People who have a known allergy or sensitivity to any of the medications used in this trial.
  • People who are unable to swallow oral (tablet or capsule) medication, or who have a condition that affects the body's ability to absorb medication properly.
  • People with an infection that is not currently under control.
  • People who have previously been treated with a drug called venetoclax, or who are currently taking part in another clinical trial involving an experimental treatment.

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 27 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

Phone: 8615948027438

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
Yehui Tan
Registry
ClinicalTrials.gov
Start date
1 June 2025
Est. completion
1 May 2029

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Modified Composite Complete Response Rate(mCRc)

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: 27 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