New stem cell combo could boost survival in blood cancer patients
NCT ID NCT07588360
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study is testing a new way to do stem cell transplants for people with acute myeloid leukemia (AML) or high-risk myelodysplastic syndromes (MDS). It combines stem cells from a half-matched donor (haploidentical) with cord blood, given at different times. The goal is to help the body accept the new cells faster, lower the chance of the cancer coming back, and improve long-term survival. About 180 people aged 14 to 60 will take part.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
About 82 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Oct 2025
- Expected to finish
-
Jun 2029
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
14 to 60 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age between 14 and 60 years, with no gender restriction. * Intermediate- or high-risk AML in first complete remission (CR1). * AML in second or subsequent complete remission (≥ CR2). * Relapsed or refractory AML. * Low-risk AML meeting any of the following: Failure to achieve a ≥3-log reduction in RUNX1::RUNX1T1 transcript level compared with baseline after 2 consolidation cycles, or loss of major molecular remission (MMR) within 6 months; CBFB::MYH11/ABL ratio \> 0.1% at any time point after 2 consolidation cycles in patients with CBFB::MYH11-rearranged AML; Presence of D816 KIT mutation in patients with CBFB::MYH11-rearranged AML; Flow cytometry-positive MRD at any time point after 2 consolidation cycles in patients with CEBPA double-mutant AML; Persistently positive MRD after chemotherapy in patients with NPM1-mutated AML. * Intermediate-2 or high-risk MDS according to the IPSS scoring system. * Adequate general health status and ability to tolerate hematopoietic stem cell transplantation. * Provision of signed informed consent and willingness to comply with study-required follow-up and examinations. Exclusion Criteria: * Prior history of other hematopoietic stem cell transplantation. * History of ex vivo T-cell-depleted stem cell transplantation. * Survival duration of less than 1 month after transplantation. * Severe organ dysfunction, including significant impairment of hepatic, renal, cardiac, or pulmonary function. * Active severe infection, such as uncontrolled pneumonia, sepsis, or other systemic infections. * History of severe hypersensitivity reactions to study medications, including cyclophosphamide or anti-thymocyte globulin (ATG). * Presence of severe psychiatric disorders or cognitive impairment that precludes compliance with study treatment and follow-up. * Pregnant or lactating women. * Concurrent malignancy of other organ system. * Any other medical conditions deemed inappropriate for study participation by the treating investigators.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for AML - acute myeloid leukemia are added.
By submitting, you agree to our Terms of use
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
4 sites. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
Chinese PLA General Hospital
NOT_YET_RECRUITINGBeijing, China
-
Fujian Medical University Union Hospital
RECRUITINGFuzhou, Fujian, 350001, China
-
Guangdong Provincial People's Hospital
NOT_YET_RECRUITINGGuangzhou, Guangdong, China
-
Sichuan Provincial People's Hospital
NOT_YET_RECRUITINGChengdu, Sichuan, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Engineered immune cells take aim at a shared marker in two blood cancers
- Can a drug duo keep High-Risk blood cancers at bay after transplant?
- Can a tropical tea shrink blood cancers?
- Can a new pill boost the power of an existing leukemia treatment?
- Can a pill tackle Tough-to-Treat leukemia?
- Can a pill and injection combo beat AML without harsh chemo?