Phase 2 Leukaemia Trial, Recruiting NCT07563179 Sponsor: Shenzhen University General Hospital Condition: Leukaemia
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Phase 2 Leukaemia Trial, Recruiting

NCT07563179
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:

  • You are between 18 and 70 years old (inclusive)
  • You have been diagnosed with acute myeloid leukemia (AML), but not the subtype called "M3" (also known as APL)
  • Your AML meets at least one of these situations: your leukemia did not go into remission after standard chemotherapy; your remission lasted 12 months or less; your remission lasted more than 12 months but the leukemia came back and at least one further chemotherapy treatment did not work; or your leukemia has relapsed after two or more previous treatments
  • You are generally well enough to carry out light activity or self-care (your doctor will assess this using a standard scale)
  • Your doctors estimate you have a life expectancy of at least 3 months
  • Your heart is pumping well enough (confirmed by an ultrasound scan of the heart)
  • Your kidneys are working well enough (confirmed by blood tests)
  • Your liver is working well enough (confirmed by blood tests)
  • Your oxygen levels are satisfactory when breathing normal room air
  • You are able to swallow tablets or capsules and follow the study requirements
  • You are willing to take part and sign a consent form

Who may not be able to join:

  • You have a known allergy or sensitivity to any of the study drugs or their ingredients
  • Your leukemia is currently active in your brain or spinal fluid (though people who previously had this but are now in stable remission may still be eligible — confirm with trial site)
  • You have an active infection (bacterial, viral, or fungal) that is not under control
  • You have a known inherited condition that affects bleeding or blood clotting, a history of bleeding episodes not caused by injury, or blood clots in your veins or arteries
  • You have an active hepatitis B infection with detectable virus in your blood
  • You have hepatitis C antibodies and detectable hepatitis C virus in your blood
  • You are HIV positive
  • You have tested positive for syphilis
  • You are currently experiencing significant bleeding, have had a serious bleeding episode in the 4 weeks before joining, or have a known inherited bleeding disorder such as haemophilia
  • You have serious heart problems, including severe heart failure, a heart attack or major heart surgery within the past 6 months, significant irregular heart rhythms, or severe disease of the heart muscle
  • You have another cancer diagnosis, past or present (with the exception of certain treated skin cancers or early-stage cervical changes — confirm with trial site)
  • You have a significant brain or nervous system condition, such as epilepsy, previous stroke, or a psychiatric disorder, that could affect your ability to safely take part
  • You have taken part in another interventional clinical trial within the last 30 days
  • You are pregnant, breastfeeding, or planning to become pregnant during the study or within 6 months after finishing, and are unwilling to use effective contraception
  • You have a known or suspected problem with drug misuse or alcohol dependence
  • You need to take certain medications that strongly affect how the study drug is processed by the body and these cannot be stopped or adjusted (confirm with trial site)
  • Your doctor believes there is any other reason that taking part would not be safe or appropriate for you

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

Principal Investigator: Shujiao He, Dr, Shenzhen University

Phone: 075521837489

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
Shenzhen University General Hospital
Registry
ClinicalTrials.gov
Start date
21 April 2026
Est. completion
30 June 2029

Where this trial is recruiting

🇨🇳 China

Primary endpoints

MRD

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