Leukaemia Trial, Recruiting NCT07588594 Sponsor: Peking University People's Hospital Condition: Leukaemia
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Leukaemia Trial, Recruiting

NCT07588594
Recruiting Not Applicable

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 aged 18 or older, of any sex or gender
  • People who have been diagnosed with chronic myelomonocytic leukemia (CMML) according to 2022 medical classification standards
  • People whose CMML is rated as intermediate-2 or high-risk using specific scoring tools (CPSS or CPSS-mol), and who are already planned to receive a stem cell transplant from a donor
  • People who have a suitable stem cell donor available — the level of genetic matching required depends on whether the donor is a half-matched family member, an unrelated donor, or a fully matched sibling (confirm specific matching details with the trial site)
  • People whose overall health and organ function meet specific standards, including a low score on a transplant health assessment tool (HCT-CI score of 2 or lower)
  • People whose heart is pumping effectively (at least 50% efficiency) and who do not have uncontrolled heart rhythm problems
  • People whose liver and kidney function blood test results fall within acceptable ranges
  • People whose blood oxygen level at rest is above 92%
  • People whose lung function tests meet minimum levels for two specific measures (confirm details with trial site)
  • People who are well enough to carry out basic daily activities (rated 0–2 on a standard health performance scale)
  • People who agree not to participate in any other interventional clinical trial during the treatment period
  • People who are willing and able to give written consent and follow the study requirements

Who may not be able to join:

  • People who have previously had a donor stem cell transplant for CMML that later came back
  • People who are unwilling or unable to receive the treatment used in this study
  • People with active hepatitis B or C, chronic active hepatitis, or a known HIV infection
  • People with an active, uncontrolled infection — including signs such as unstable blood pressure related to infection, worsening infection symptoms, new infection areas visible on scans, or unexplained ongoing fever
  • People who have had a stroke or bleeding in the brain within the 6 months before joining
  • People who are currently pregnant or breastfeeding
  • People who have been diagnosed with another type of cancer within the past 2 years — with some exceptions for certain early-stage or treated cancers (confirm specific exceptions with the trial site)
  • People who have any other condition that the trial doctor considers 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 28 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Yuqian Sun, MD, Peking University People's Hospital

Phone: +86 13717833825

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
Not Applicable
Sponsor
Peking University People's Hospital
Registry
ClinicalTrials.gov
Start date
13 February 2026
Est. completion
1 May 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

One-year relapse-free survival (RFS) after allogeneic hematopoietic stem cell transplantation

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