Study of VA Combined With HAAG Regimen in Newly Diagnosed Intermediate and High-risk AML Patients
Recruiting
Phase 2
Interventional Study
Intermediate Risk Acute Myeloid Leukemia
High Risk Acute Myeloid Leukemia
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
At a Glance
- Age
- 18 – 65
- Sex
- Any
- Trial phase
- Phase 2
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 60 (estimated)
- Sponsor
- The First Affiliated Hospital of Soochow University · Other
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About This Trial
The purpose of this study is to evaluate the efficacy and safety of VA combined with HAAG in the induction treatment of newly diagnosed acute myeloid leukemia.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
1. Newly diagnosed intermediate and high-risk AML according to the WHO (2022) classification of acute myeloid leukemia (non-APL).
2. Age 18-65.
3. ECOG score: 0-2.
4. No history of previous chemotherapy or target therapy.
5. Serum total bilirubin \<= 2 times the upper limit of n…
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