Venetoclax in Combination With Ivosidenib and Azacitidine for Newly Diagnosed IDH1-Mutated AML

NCT06611839 | Recruiting Phase 1

• 1 other identifier: IIT2024067
• Study Type: interventional
• Target: 29
• Locations: 1 country
• Sites: 1

Brief Summary

Venetoclax can bind to the BCL-2 protein, thereby initiating the apoptosis program and exerting anti-AML effects. The induction regimen combining venetoclax with hypomethylating agents (HMA) significantly improves the remission rate (over 60%) in elderly unfit AML patients and markedly prolongs survival in those achieving complete remission. Isocitrate dehydrogenase (IDH) 1 and 2 are involved in the citric acid cycle. Approximately 20% of AML patients carry IDH1 or IDH2 mutations, which lead to the reduction of α-ketoglutarate to 2-hydroxyglutarate (2-HG). 2-HG can cause histone methylation and inhibit TET2 activity, resulting in DNA hypermethylation, thereby affecting gene expression and cell differentiation. IDH mutations are more common in elderly patients and are often associated with cytogenetic abnormalities; they may also co-occur with FLT3-ITD, NPM1, or DNMT3A mutations. Ivosidenib is an IDH1 inhibitor, and previous studies have confirmed its safety and efficacy in AML treatment. According to adult AML treatment guidelines, IDH-mutated patients eligible for intensive chemotherapy may receive IDH inhibitors during induction therapy. Based on the study by Montesinos et al. on the role of ivosidenib and azacitidine in IDH-mutated AML, for patients ineligible for intensive chemotherapy, a new treatment option has been added: IDH1-mutated AML patients may receive ivosidenib (500 mg, days 1-28) combined with azacitidine (75 mg/m²/day for 7 days) in 28-day cycles, or ivosidenib monotherapy. Recent studies have shown that a triple-drug regimen comprising ivosidenib, venetoclax, and azacitidine demonstrates excellent efficacy and safety. In chemotherapy-ineligible patients, the triple regimen achieved a composite complete remission rate (CRc) of 86% and an overall response rate (ORR) of 92%. At a median follow-up of 27.4 months, the 2-year overall survival (OS) was 72%, and the 2-year event-free survival (EFS) was 72%. Therefore, this study aims to conduct a multicenter, single-arm clinical trial to determine the maximum tolerated dose of the triple-drug regimen (ivosidenib, venetoclax, and azacitidine) and preliminarily evaluate the long-term efficacy of this combination. Additionally, it seeks to elucidate the relationship between measurable residual disease (MRD) levels and the selection of transplantation treatment strategies, providing evidence for MRD-based therapeutic decision-making.

Conditions

AML; IDH1 Mutation; Treatment

Outcome Measures

Primary Outcomes (4)

• CRc rate

  The ratio of patients achieved CR/CRh/CRi.

  Efficacy was assessed at least 2 weeks after completion of the first course of induction therapy.

• CRc MRD negtive rate by flow cytometry

  The CRc MRD negtive rate was detected by flow cytometry after induction, consolidation and maintenance therapy.

  Efficacy was assessed at least 2 weeks after completion of the first course of induction therapy.

• CRc MRD negtive rate by PCR

  The CRc MRD negtive rate was detected by PCR after induction, consolidation and maintenance therapy.

  Efficacy was assessed at least 2 weeks after completion of the first course of induction therapy.

• The maximum tolerated dose of ivosidenib and venetoclax combined with intensive chemotherapy

  To determine the maximum tolerated dose of ivosidenib and venetoclax combined with intensive chemotherapy

  up to 3 months after enrollment of the first participants

Secondary Outcomes (5)

• Event-free survival (EFS)

  up to 2 years after the date of the last enrolled participants

• overall survival

  up to 2 years after the date of the last enrolled participants

• Relapse free survival

  up to 2 years after the date of the last enrolled participants

• 30-day mortality

  Within 30 days of the date of the last enrolled participants

• 60-day mortality

  Within 60 days of the date of the last enrolled participants

Study Arms (1)

Venetoclax、Ivosidenib and Azacitidine

EXPERIMENTAL

The study was divided into two phases: dose climbing (phase I)and dose extension (phase II).

Drug: Ivosidenib, Venetoclax, Azacitidine

Interventions

Ivosidenib, Venetoclax, Azacitidine DRUG

phase I: Induction therapy：Ivosidenib 、Venetoclax、Azacitidine Dose climbing stage: adopt the 3 + 3 design principle, and the dose level 0,-1and 1 are set as follows dose level 0: Ivosidenib 500mg d1-28 Venetoclax 100mg d-3，200mg d-2，400mg d-1,800mg d1-14 Azacitidine 75mg/m2/d, d1-7 dose level -1:Ivosidenib 500mg d1-28 Venetoclax 100mg d-3，200mg d-2，400mg d-1, 600mg d1-14 Azacitidine 75mg/m2/d, d1-5 dose level 1:Ivosidenib 500mg d1-28 Venetoclax 100mg d-3，200mg d-2，400mg d-1 800mg d1-21 Azacitidine 75mg/m2/d, d1-7 Consolidation therapy intermediate-dose cytarabine regimen ： 3 courses If IDH1 mutant residual disease was positive before consolidation chemotherapy, Ivosidenib was added; Maintenance treatment: Azacitidine、Venetoclax 、Ivosidenib： 6 courses phase II: dose based on phase I results

Venetoclax、Ivosidenib and Azacitidine

Eligibility Criteria

• Age: 14 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

• Patients who meet AML according to WHO (2022) or AML and MDS/AML defined by ICC standards with IDH1 mutations detected by PCR or second-generation sequencing.
• Age ≥14 years old, male or female.
• The physical status assessment (ECOG-PS) of the Eastern Oncology Collaboration group was 0-2 points.
• Fulfill the requirements of the following laboratory tests (performed within 7 days prior to treatment) :
• Total bilirubin ≤ 1.5 times the upper limit of normal value (same age);
• AST and ALT≤ 2.5 times the upper limit of normal value (same age);
• Blood creatinine \< 2 times the upper limit of normal (same age);
• Myocardial enzymes \< 2 times the upper limit of normal (same age);
• Left ventricular ejection fraction \>50% by measure of echocardiogram (ECHO) Informed consent must be signed before the commencement of all specific study procedures, and is signed by the patient himself or his immediate family. Considering the patient\'s condition, if the patient\'s signature is not conducive to the treatment of the condition, the informed consent shall be signed by the legal guardian or the patient\'s immediate family.

You may not qualify if:

• Subjects who meet any of the following criteria are excluded from the study:
• Acute promyelocytic leukemia with PML-RARA fusion gene
• Acute myeloid leukemia with RUNX1-RUNX1T1 or CBFB-MYH11 fusion gene
• Acute myeloid leukemia with BCR-ABL fusion gene
• Treated patients (but can receive hydroxyurea or cytarabine to lower tumor burden).
• Concurrent malignant tumors of other organs (those requiring treatment).
• Active heart disease, defined as one or more of the following:
• A history of uncontrolled or symptomatic angina;
• Myocardial infarction less than 6 months after enrollment;
• Have a history of arrhythmia requiring drug treatment or severe clinical symptoms;
• Uncontrolled or symptomatic congestive heart failure (\> NYHA level 2);
• Serious infectious diseases (uncured tuberculosis, pulmonary aspergillosis).

Sponsors & Collaborators

• Institute of Hematology & Blood Diseases Hospital, China: lead

Study Sites (1)

Blood Diseases Hospital

Tianjin, Tianjin Municipality, 300020, China

RECRUITING

MeSH Terms

Interventions

ivosidenib; venetoclax; Azacitidine

Intervention Hierarchy (Ancestors)

Aza Compounds; Organic Chemicals; Cytidine; Pyrimidine Nucleosides; Pyrimidines; Heterocyclic Compounds, 1-Ring; Heterocyclic Compounds; Nucleosides; Nucleic Acids, Nucleotides, and Nucleosides; Ribonucleosides

Study Officials

• Hui Wei, MD

  Blood diseases hospital

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Hui Wei, MD

CONTACT

13132507161; weihui@ihcams.ac.cn

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: OTHER
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: September 19, 2024
• First Posted: September 25, 2024
• Study Start: October 17, 2025
• Primary Completion (Estimated): October 1, 2026
• Study Completion (Estimated): October 1, 2028
• Last Updated: February 11, 2026

Record last verified: 2025-09

Locations

CN (1)