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OncoMatch/Clinical Trials/NCT05603884

VCA Regimen Followed by D-MAG Regimen on the Treatment of Elderly Patients With Newly Diagnosed Acute Myeloid Leukemia (AML)

Is NCT05603884 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies Venetoclax Combining Chidamide and Azacitidine (VCA) regimen followed by dicitabine combined with liposome mitoxantrone, cytarabine, and G-CSF (D-MAG) regimen for leukemia, myeloid, acute.

Phase 2RecruitingThe First Affiliated Hospital of Xiamen UniversityNCT05603884Data as of Jun 2026Location: China

Treatment: Venetoclax Combining Chidamide and Azacitidine (VCA) regimen followed by dicitabine combined with liposome mitoxantrone, cytarabine, and G-CSF (D-MAG) regimenThe purpose of this study is to evaluate the safety and efficacy of Venetoclax Combining Chidamide and Azacitidine (VCA) Followed by D-MAG Regimen on the Treatment of Elderly Patients With Newly Diagnosed Acute Myeloid Leukemia (AML)

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Extracted eligibility criteria

Treatments studied

Other

Venetoclax Combining Chidamide and Azacitidine (VCA) regimen followed by dicitabine combined with liposome mitoxantrone, cytarabine, and G-CSF (D-MAG) regimen

Cancer type

Acute Myeloid Leukemia

Biomarker criteria

Excluded: BCR ABL1 translocation

chronic myeloid leukemia (CML) with or without BCR-ABL1 translocation and AML with BCR-ABL1 translocation

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Demographics

Ages ≥ 60

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Cannot have received: hypomethylating agent

Participants have received the following treatments: hypomethylating agents

Cannot have received: (venetoclax)

Participants have received the following treatments: veneclax

Cannot have received: chemotherapy

Participants have received the following treatments: chemotherapy for myelodysplastic syndrome (MDS)

Cannot have received: solid organ transplantation

Participants have received the following treatments: solid organ transplantation

Lab requirements

Kidney function

estimated creatinine clearance ≥ 30 ml/min

Liver function

ast and alt ≤ 3.0 x uln (unless leukemic organ involvement). bilirubin ≤ 1.5 x uln (unless considered due to leukemic organ involvement)

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT05603884 currently recruiting?

Yes, this trial is currently recruiting patients.

Can patients have received prior systemic therapy?

No. This trial requires treatment-naive patients — prior systemic therapy is an exclusion criterion.

Are patients with BCR alterations eligible?

No. BCR ABL1 translocation is an exclusion criterion.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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