Phase 2 Leukaemia Trial, Recruiting NCT06754267 Sponsor: First Affiliated Hospital of Zhejiang University Condition: Leukaemia
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Phase 2 Leukaemia Trial, Recruiting

NCT06754267
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 newly diagnosed with a specific type of blood cancer called precursor B-cell acute lymphoblastic leukemia (B-ALL) that has a genetic marker known as the Philadelphia chromosome, confirmed by specific laboratory tests
  • People who are 18 years of age or older
  • People whose overall health and ability to carry out daily activities falls within an acceptable range, as measured by a standard medical scoring system (scores 0–2 on the ECOG scale — confirm with trial site)
  • People whose life expectancy is at least 3 months
  • People whose organs (such as heart, liver, and kidneys) are functioning well enough to allow participation in this trial
  • People who understand the study and are willing to sign a consent form agreeing to take part
  • People (and their partners) who are willing to use effective contraception throughout the treatment period and for at least 12 months after the last dose of the study drug — this applies to men and to women who could become pregnant (women who have been through menopause for at least 12 months are considered unable to become pregnant)

Who may not be able to join:

  • People whose leukemia is considered to have developed from a more advanced stage of a different blood cancer called chronic myeloid leukemia (CML)
  • People whose leukemia has spread to the brain, spinal cord, or areas outside the bone marrow
  • People who have already received any systemic treatment for leukemia, such as targeted therapy, chemotherapy, or radiation therapy (some limited pre-treatment may be allowed — confirm with trial site)
  • People who have had a heart attack within the past 12 months, or who have serious heart conditions such as uncontrolled high blood pressure, uncontrolled irregular heartbeat, congestive heart failure, or unstable chest pain; or whose heart pumping function is below a certain level on an ultrasound test (less than 50%)
  • People who have significant problems with their lungs, liver, or kidneys — including but not limited to severe infections, uncontrolled diabetes, active tuberculosis, asthma, COPD, or certain lung conditions
  • People who have had another type of cancer in the past 5 years, with the exception of certain localised thyroid cancers or skin cancers that have not spread
  • People whose blood test results show that liver or kidney function is outside acceptable limits (specific lab thresholds apply — confirm with trial site)
  • People who are known to have HIV infection
  • People who have any other condition that the trial doctor believes would interfere with the safe use of the study treatment
  • People who are unable to understand or follow the requirements of the study

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.

Contact this trial

Principal Investigator: Jie Jin, Zhejiang University

Phone: +8657187236896

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
First Affiliated Hospital of Zhejiang University
Registry
ClinicalTrials.gov
Start date
1 December 2024
Est. completion
30 December 2025

Where this trial is recruiting

🇨🇳 China

Primary endpoints

complete molecular response (CMR) after three cycles

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