VA Consolidation in Intermediate-Risk AML
This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.
About the trial
This clinical trial aims to compare the efficacy and safety of venetoclax-based consolidation therapy versus conventional consolidation chemotherapy (intermediate/high-dose cytarabine) in newly diagnosed adult patients with intermediate-risk acute myeloid leukemia (AML). Participants must have achieved complete remission (CR) or CR with incomplete hematologic recovery (CRi) after induction therapy with venetoclax and azacitidine and are planned to undergo allogeneic hematopoietic stem cell transplantation (allo-HSCT).
Original English text from ClinicalTrials.gov
Who can (and can't) join
✓ Qualifies
- •Potwierdzona diagnoza białaczki ostroleukemii
- •Wiek 18 lat lub więcej
- •Białaczka klasyfikowana jako pośredniego ryzyka
- •Uzyskanie remisji (ustąpienia choroby) po leczeniu venetoclaxem i azacytydyną
- •Posiadanie dawcy do przeszczepu szpiku kostnego
- •Dobra sprawność fizyczna i funkcje organów
✗ Disqualifies
- •Poważne problemy sercowo-naczyniowe lub niedawny zawał
- •Białaczka w ośrodkowym układzie nerwowym
- •Inne groźne choroby uniemożliwiające udział w badaniu
- •Zakażenie HIV lub ciężka niewyleczona hepatitis
- •Ciąża lub karmienie piersią
- •Niezdolność do zrozumienia i przestrzegania wymogów badania
Simplified criteria — AI translation
Trial details
- Minimum age
- 18 Years
- Last updated (source)
- August 6, 2026
- Sex
- No restrictions
Therapies / drugs in trial
Locations (1)
The First Affiliated Hospital of Soochow University
Suzhou, China
Trial contact
Contact information from ClinicalTrials.gov. Contact in English.
Share this trial
Data from ClinicalTrials.gov. AI-assisted translation, last sync: 8/7/2026.
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