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Allogeneic Hematopoietic Stem Cell Transplantation with Mobilizing Agent-Enhanced Pretreatment for Myeloid Malignancies

Allogeneic Hematopoietic Stem Cell Transplantation with Mobilizing Agent-Enhanced Pretreatment for Myeloid Malignancies

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500110598
Enrollment
Unknown
Registered
2025-10-16
Start date
2025-10-20
Completion date
Unknown
Last updated
2026-03-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Myeloid Malignancies

Interventions

Intervention group:1. Venetoclax: Administered orally at 400 mg/day for 5 days, from day -7 to day -3. 2. Decitabine (Dec): Administered by intravenous infusion at 20 mg/m^2/day for 5 days, from day -

Sponsors

Xiangya hospital central south university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosed with a myeloid malignancy (according to the WHO 2022 criteria); 2. Aged 18 to 70 years, inclusive; 3. Predicted to be at high or very high risk, or with refractory/relapsed disease; 4. Availability of a suitable healthy hematopoietic stem cell donor; 5. ECOG performance status of <= 2; 6. Voluntarily signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Active infection not under control (e.g., bacteremia, invasive fungal infection); 2. Severe organ dysfunction (LVEF =2×ULN, ALT >=3×ULN); 3. History of prior hematopoietic stem cell transplantation (HSCT) or solid organ transplantation; 4. Pregnant or lactating women; 5. Other conditions deemed unsuitable for allo-HSCT by the investigator.

Design outcomes

Primary

MeasureTime frame
Time to neutrophil engraftment;

Secondary

MeasureTime frame
100-day non-relapse mortality (NRM); incidence of grade III-IV acute GVHD;Change from baseline in the Quality of Life score (EORTC QLQ-C30);Change from baseline in the Symptom Burden score (MDASI);2-year Overall Survival (OS) rate;2-year Relapse-Free Survival (RFS) rate;

Countries

China

Contacts

Public ContactFu Bin

Xiangya hospital central south university

xyfubin@126.com+86 731 8975 3731

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 3, 2026