Phase 2 Leukaemia Trial, Recruiting NCT07514832 Sponsor: Beijing 302 Hospital Condition: Leukaemia
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Phase 2 Leukaemia Trial, Recruiting

NCT07514832
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 diagnosed with acute myeloid leukemia (AML, but not the subtype called acute promyelocytic leukemia), confirmed through standard lab and genetic testing using 2022 diagnostic guidelines
  • People aged 18 to 70 years old, of any gender
  • People who have not yet received any treatment for AML (a short course of a medication like hydroxyurea to control white blood cell counts during diagnosis is allowed)
  • People who have been assessed by a doctor as being able to tolerate intensive chemotherapy, based on a specific medical assessment framework
  • People whose general physical functioning is rated at a certain level (a score of 2 or below on a standard medical scale, meaning they are able to care for themselves but may not be able to do heavy physical work)
  • People whose kidney function test results fall within acceptable ranges for this trial
  • People whose liver function test results fall within acceptable ranges for this trial
  • People whose heart pumping function is at or above a minimum level (45% or within normal range, as measured by an ultrasound of the heart)
  • People whose life expectancy is estimated to be more than 3 months

Who may not be able to join:

  • People who have a history of certain blood or bone marrow conditions, including myelofibrosis, essential thrombocythemia, polycythemia vera, chronic myeloid leukemia, or a specific subtype of AML linked to a particular gene change (BCR-ABL1)
  • People who have previously been treated with venetoclax or azacitidine for any condition
  • People who have a known allergy or sensitivity to any ingredient in the trial medications
  • People who have been diagnosed with another cancer within the past 2 years, with some exceptions — certain early-stage or fully treated skin cancers, cervical or breast carcinoma in situ, or cancers previously treated with curative surgery or similar methods may still be considered eligible (confirm with trial site)
  • People who have a severe infection that is not under control, or who have active uncontrolled bleeding
  • People who are pregnant or currently breastfeeding
  • People who have an active, uncontrolled infection with HIV, hepatitis B, or hepatitis C
  • People who show signs of leukemia that has spread to the brain or spinal fluid before treatment begins
  • People of childbearing potential who are not willing to use at least one reliable form of contraception from the start of the trial until 90 days after the last dose, and male participants who are not willing to use contraception or to avoid donating sperm during the same period
  • People who have epilepsy requiring ongoing medication, dementia, or other significant mental health conditions that would affect their ability to understand or follow the trial requirements
  • People with psychiatric conditions or thinking difficulties that would prevent them from cooperating with treatment and follow-up, or conditions that prevent them from swallowing tablets or absorbing medication through the gut

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 8 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: 86+01066947169

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
Beijing 302 Hospital
Registry
ClinicalTrials.gov
Start date
15 April 2026
Est. completion
1 April 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Composite complete response 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: 8 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