Phase 2 Leukaemia Trial, Recruiting NCT07028086 Sponsor: Ruijin Hospital Condition: Leukaemia
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Phase 2 Leukaemia Trial, Recruiting

NCT07028086
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 fully understand the study, choose to take part voluntarily, and sign a consent form
  • People aged between 18 and 65 years old
  • People who have been diagnosed with acute myeloid leukemia (a type of blood cancer, but not a specific subtype called APL) that has not yet been treated, and who also meet at least one of the following: their leukemia developed from a prior blood condition (secondary AML); their leukemia developed as a result of previous cancer treatment (therapy-related AML); their leukemia has spread outside the bone marrow to form a tumour (myeloid sarcoma); or they are aged 60 or older and have been assessed by doctors as healthy enough to receive intensive treatment
  • People whose heart is working well, with the heart's pumping strength (called ejection fraction) at 50% or above
  • People whose liver and kidney blood test results fall within acceptable ranges as determined by the trial team
  • People whose general health and ability to carry out daily activities is rated at a level of 0, 1, or 2 on a standard medical scale (where 0 means fully active and 2 means able to care for oneself but unable to do physical work)

Who may not be able to join:

  • People whose leukemia has been assessed by doctors as making them too unwell or too frail to tolerate intensive treatment
  • People who have, or have had, another type of cancer that currently requires treatment
  • People with serious uncontrolled health conditions, such as a severe active infection or high blood pressure that cannot be managed
  • People who have had a significant allergic reaction to medications in the same family as the drugs used in this trial
  • People who are pregnant or breastfeeding, or people who are unwilling to use reliable contraception throughout the study period
  • People with a history of serious neurological or psychiatric conditions
  • People with serious heart conditions, such as a previous heart attack, severe chest pain, or serious heart rhythm problems
  • People who have had a stroke or a temporary stroke-like episode (confirm with trial site)
  • People with a known HIV infection, or an active hepatitis B or C infection (note: people who are inactive carriers of hepatitis, or who have low virus levels while receiving certain antiviral treatments, may not be automatically excluded — confirm with trial site)
  • People who have taken certain medications or consumed certain foods that affect how the body processes drugs (specifically, strong or moderate CYP3A inducers or inhibitors, or strong P-gp inhibitors) within the 7 days before starting the trial treatment
  • People who are unable to swallow tablets or capsules, or who have a condition that prevents the body from properly absorbing oral medications
  • People whom the trial doctors determine are not suitable for the study for any other reason

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 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.

GP referral letter

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Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Registry
ClinicalTrials.gov
Start date
20 June 2025
Est. completion
1 June 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Composite Complete Remission Rate

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