Phase 2 Leukaemia Trial, Recruiting NCT07304232 Sponsor: Institute of Hematology & Blood Diseases Hospital, China Condition: Leukaemia
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Phase 2 Leukaemia Trial, Recruiting

NCT07304232
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 leukaemia (AML) according to specific 2022 medical guidelines, whose leukaemia showed intermediate- or high-risk chromosome abnormalities, and whose disease went into complete remission (no detectable cancer) after a stem cell transplant from a donor.
  • People whose leukaemia remained in complete remission after the transplant.
  • People who are enrolling between 60 and 100 days after their transplant.
  • People aged 18 to 75 years.
  • People who are in good general physical condition, able to carry out normal daily activities with little or no limitation (confirm with trial site for exact fitness level required).
  • People whose kidney function blood test results are within an acceptable range (below 1.5 times the upper limit of normal for creatinine).
  • People whose liver function results are within acceptable ranges — specifically, direct bilirubin below 1.5 mg/dL (with an exception for those with a condition called Gilbert's syndrome), and liver enzyme levels (ALT and AST) below 2.5 times the upper limit of normal.
  • People who are able to understand the trial information and sign a written consent form.

Who may not be able to join:

  • People who have received any other experimental or investigational medications after their transplant.
  • People whose leukaemia has a specific genetic change called an FLT3 mutation.
  • People whose leukaemia has spread to the brain or spinal cord.
  • People experiencing uncontrolled moderate-to-severe graft-versus-host disease (a condition where donor cells attack the body) after their transplant.
  • People with an active infection that is not currently under control.
  • People with a known or suspected allergy or sensitivity to the study drug (Chidamide) or any of its ingredients.
  • People with uncontrolled heart failure or other serious ongoing health conditions that, in the treating doctor's judgement, would make participation unsafe or interfere with assessing the treatment.
  • People who are pregnant or breastfeeding.
  • People who have any other condition that, in the treating doctor's judgement, would make participation unsuitable.

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: +86-15122538106

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
Institute of Hematology & Blood Diseases Hospital, China
Registry
ClinicalTrials.gov
Start date
1 September 2025
Est. completion
31 December 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Recurrence-Free Survival(RFS)

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