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A Phase 2 Study of MAX-40279 Combined With Venetoclax and Azacitidine in Unfit Newly Diagnosed Acute Myeloid Leukemia

29. juli 2026 opdateret af: Maxinovel Pty., Ltd.
This is a prospective, multicenter, phase Ⅱ study consisting of dose escalation and ex-pansion stages in unfit newly diagnosed AML.

Studieoversigt

Status

Rekruttering

Betingelser

Detaljeret beskrivelse

This is a prospective, multicenter, phase Ⅱ study consisting of dose escalation and ex-pansion stages in unfit newly diagnosed AML. Patients in dose escalation stage received oral MAX-40279 at three doses, in combination with VEN and AZA in 28-day cycles. Three to six patients were enrolled at each dose level. The dose limiting toxicities (DLTs) observation period was 28 days after the first dose. All evaluable patients with ≥1 cycle treatment were included in preliminary efficacy analysis.

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

43

Fase

  • Fase 2

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Studiesteder

      • Tianjin, Kina
        • Rekruttering
        • Institute of Institute of Hematology & Blood Diseases Hospital ( Chinese Academy of Medical Sciences)
        • Kontakt:

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ingen

Beskrivelse

Inclusion Criteria:

1. Patients meeting the World Health Organization (WHO) 2016 diagnostic criteria for newly diagnosed acute myeloid leukemia (AML) patients unfit for intensive chemotherapy:

  1. Age ≥65 years, or
  2. Age >18 years and ineligible for standard-dose chemotherapy, defined by ≥1 of the following:

ECOG performance status 2 or 3;History of chronic heart failure (CHF) requiring treatment or left ventricular ejection fraction (LVEF) ≤50% DLCO ≤65% or FEV1 ≤65%Creatinine clearance ≥30 mL/min but ≤45 mL/min (Cockcroft-Gault)、Any other condition deemed incompatible with standard chemotherapy (requires PI approval) 2. No prior AML therapy, except:Hydroxyurea. 3. ECOG performance status ≤3 4. Laboratory requirements: WBC≤3×10*9/L、AST/ALT/ALP ≤3×ULN (except: due to leukemic involvement)、Total bilirubin ≤1.5×ULN、Serum creatinine clearance ≥30 mL/min (measured or calculated) 5. Life expectancy ≥3 months 6. Contraception requirements: Negative pregnancy test for women of childbearing potential;Agreement to use effective contraception during treatment and for 6 months after therapy

Exclusion Criteria:

  1. AML with BCR::ABL1 fusion、Acute promyelocytic leukemia (APL).
  2. Secondary AML, including:Therapy-related AML (per WHO classification)、AML with prior history of myelodysplastic syndrome (MDS) or myeloproliferative neoplasm (MPN).
  3. Use of strong/moderate CYP3A4 inducers within 3 days prior to treatment initiation.
  4. Hypersensitivity to any study drugs.
  5. Active malignancy in other organs (requiring treatment).
  6. Active cardiac disease, defined as ≥1 of the following:Myocardial infarction within 6 months before enrollment;History of symptomatic arrhythmia requiring medication;Uncontrolled/symptomatic congestive heart failure (NYHA Class >2)
  7. Active infections, including:Untreated tuberculosis or any aspergillosis.
  8. Known HIV, active hepatitis B (HBV), or hepatitis C (HCV).
  9. Central nervous system (CNS) leukemia at baseline.
  10. Conditions limiting oral drug absorption (e.g., malabsorption syndrome).
  11. Medical history of:Epilepsy requiring medication、Dementia or psychiatric disorders impairing protocol compliance.
  12. Investigator's discretion for ineligibility.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Interventionel model: Enkelt gruppeopgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: MAX-40279 Combined with Venetoclax and Azacitidine in unfit newly diagnosed AML

Patients in dose escalation stage received oral MAX-40279 at 40 mg, 50 mg, and 60 mg twice daily (BID), in combination with VEN (100 mg on day 1, 200 mg on day 2, and 400 mg daily thereafter) and AZA (75 mg/m2 days 1-7) in 28-day cycles.

Patients in dose expansion stage received RP2D MAX-40279 plus VEN (100 mg on day 1, 200 mg on day 2, and 400 mg daily thereafter) and AZA (75 mg/m2 days 1-7).

Dose escalation:MAX-40279: 40 mg, 50 mg, and 60 mg twice daily (BID). Dose expantion: MAX-40279 RP2D.

Venetoclax: 100 mg on day 1, 200 mg on day 2, and 400 mg daily thereafter. Azacitidine: 75 mg/m2 days 1-7. 28 days are one cycle.

Given by IV, 75 mg/m2
Andre navne:
  • Vidaza
100 mg on day 1, 200 mg on day 2, and 400 mg daily thereafter.
Andre navne:
  • VENCLEXTA

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
DLT
Tidsramme: Dose escalation; an average of 6 months.
The dose limiting toxicities, Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0
Dose escalation; an average of 6 months.
Adverse events (AEs), serious adverse events (SAEs)
Tidsramme: Through study completion; an average of 24 months.
Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0
Through study completion; an average of 24 months.
Maximum Tolerated Dose (MTD) or Recommended Phase 2 Dose (RP2D)
Tidsramme: Dose escalation; an average of 6 months.
Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0
Dose escalation; an average of 6 months.
CRc
Tidsramme: Through study completion; an average of 24 months.
complete remission rate
Through study completion; an average of 24 months.

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
RFS
Tidsramme: Through study completion; an average of 8 months.
Recurrence-Free Survival
Through study completion; an average of 8 months.
DoR
Tidsramme: Through study completion; an average of 8 months.
duration of response
Through study completion; an average of 8 months.
OS
Tidsramme: Through study completion; an average of 24 months.
overall survival
Through study completion; an average of 24 months.

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Ledende efterforsker: Jianxiang Wang, MD, Institute of Institute of Hematology & Blood Diseases Hospital

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

5. september 2025

Primær færdiggørelse (Anslået)

1. september 2027

Studieafslutning (Anslået)

1. december 2027

Datoer for studieregistrering

Først indsendt

29. juli 2026

Først indsendt, der opfyldte QC-kriterier

29. juli 2026

Først opslået (Faktiske)

3. august 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

3. august 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

29. juli 2026

Sidst verificeret

1. juli 2026

Mere information

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