Phase 2 Leukaemia Trial, Recruiting NCT06429098 Sponsor: The First Affiliated Hospital of Soochow University Condition: Leukaemia
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Phase 2 Leukaemia Trial, Recruiting

NCT06429098
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 18 years of age or older
  • You have been newly diagnosed with a specific type of acute myeloid leukemia (AML) involving a genetic change called CBFβ::MYH11 (confirm with trial site)
  • Your general health and ability to carry out daily activities falls within an acceptable range, as measured by a standard medical scale (ECOG score 0–3) (confirm with trial site)
  • You are willing and able to sign a consent form before any study-related steps begin

This trial also includes people who may not be suitable for intensive chemotherapy. You may fall into this "unfit" category if at least one of the following applies to you:

  • You are older than 75 years
  • You have serious problems with your heart, lungs, kidneys, or liver
  • You have an active infection that is not responding to treatment
  • You have cognitive impairment (such as problems with memory or thinking)
  • You have other health conditions that your doctor feels make intensive chemotherapy unsuitable for you

Who may not be able to join:

  • You have already received certain types of treatment for AML, such as chemotherapy or targeted drug therapy (some exceptions may apply — confirm with trial site)
  • You are currently pregnant or breastfeeding
  • You are not able to attend all required study visits or follow all study procedures, including follow-up appointments
  • Your doctor determines there are other reasons that make this study unsuitable 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 19 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: Ying Wang, The First Affiliated Hospital of Soochow University

Phone: 008613656214782

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
The First Affiliated Hospital of Soochow University
Registry
ClinicalTrials.gov
Start date
1 January 2024
Est. completion
30 June 2027

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: 19 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