A Phase I-II Study Investigating the All-Oral Combination of the Menin Inhibitor SNDX-5613 With Decitabine/Cedazuridine (ASTX727) and Venetoclax in Acute Myeloid Leukemia (SAVE)

NCT ID: NCT05360160

Last Updated: 2025-10-23

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 43 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-10-14
• Study Completion Date: 2026-12-01

Brief Summary

Part 1b of this clinical research study is to find the highest tolerable dose of SNDX-5613 that can be given in combination with ASTX727 (a combination of the drugs decitabine/cedazuridine) and venetoclax for patients with acute myeloid leukemia (AML) or those with a mixed phenotype acute leukemia with a myeloid phenotype (MPAL).

Part 2 of this study is to learn if the dose of study drugs found in Part 1b can help to control AML/MPAL

Detailed Description

Primary Objectives:

Phase Ib

• To determine the safety, tolerability and recommended phase II dose (RP2D) of SNDX-5613 in combination with oral decitabine/cedazuridine (ASTX727) and venetoclax for patients with acute myeloid leukemia (AML).

Phase II

• To assess the efficacy of SNDX-5613 in combination with ASTX727 and venetoclax for patients with AML.

Secondary Objectives

• To assess overall survival, event-free survival and duration of response.

Exploratory Objectives

• To evaluate molecular and cellular markers that may be predictive of antitumor activity and/or resistance.

Conditions

Acute Myeloid Leukemia

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

SNDX-5613

Capsules by mouth 2 times every day (about 12 hours apart).

Group Type: EXPERIMENTAL

SNDX-5613

Intervention Type: DRUG

Given by PO

Venetoclax

Tablets by mouth on Days 1-14 of each cycle.

Group Type: EXPERIMENTAL

Venetoclax

Intervention Type: DRUG

Given by PO

ASTX727

Tablets by mouth on Days 1-5 of each cycle.

Group Type: EXPERIMENTAL

ASTX727

Intervention Type: DRUG

Given by PO

Interventions

SNDX-5613

Given by PO

Intervention Type: DRUG

Venetoclax

Given by PO

Intervention Type: DRUG

ASTX727

Given by PO

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Age ≥ 12 years with weight ≥ 40Kg.

2. ECOG performance status of ≤ 2.

3. Newly diagnosed (frontline cohort), who are not eligible for high-intensity induction chemotherapy or relapsed/refractory (R/R cohort) AML or myeloid phenotype MPAL with either KMT2Ar, or NUP98r, or NPM1c.

4. WBC must be below 25,000/ μL at time of enrollment. Patients may receive cytoreduction prior to enrollment.

5. Baseline ejection fraction must be > 40%.

6. Adequate hepatic function (direct bilirubin < 2x upper limit of normal (ULN) unless increase is due to Gilbert's disease or leukemic involvement, and AST and/or ALT < 3x ULN unless considered due to leukemic involvement, in which case direct bilirubin or AST and/or ALT < 5x ULN will be considered eligible).

7. Adequate renal function (creatinine clearance ≥ 30 mL/min) unless related to disease.

8. Willing and able to provide informed consent.

9. In the absence of rapidly proliferative disease, the interval from prior treatment to time of initiation will be at least 14 days for cytotoxic or non-cytotoxic (immunotherapy agent(s), or an interval of 5 half-lives of the prior therapy. Oral hydroxyurea and/or cytarabine (up to 2 g/m2) for patients with rapidly proliferative disease is allowed before the start of study therapy, as needed, for clinical benefit and after discussion with the PI. Concurrent therapy for central nervous system (CNS) prophylaxis or continuation of therapy for controlled CNS disease is permitted.

10. Women of childbearing potential must agree to adequate methods of contraception during the study and at least 3 months after the last treatment. Males must be surgically or biologically sterile or agree to use an adequate method of contraception during the study and at least 3 months after the last treatment.

Exclusion Criteria

1. Prior treatment with a menin inhibitor.

2. Patients with any concurrent uncontrolled medical condition, laboratory abnormality, or psychiatric illness which could place the patient at unacceptable risk of study treatment.

3. The use of other chemotherapeutic agents or anti-leukemic agents is not permitted during study with the following exceptions (1) intrathecal chemotherapy for prophylactic use or for controlled CNS leukemia. (2) use of hydroxyurea for patients with rapidly proliferative disease or for control of counts during differentiation syndrome. (3) use of steroids for treatment of differentiation syndrome.

4. Patients with any severe gastrointestinal or metabolic condition which could interfere with the absorption of oral study medications.

5. Patients with a concurrent active malignancy under treatment.

6. Known active hepatitis B (HBV) or Hepatitis C (HCV) infection or known HIV infection.

7. Female subjects who are pregnant or breast-feeding.

8. Patient has an active uncontrolled infection.

9. Any of the following within the 6 months prior to study entry: myocardial infarction, uncontrolled/unstable angina, congestive heart failure (New York Heart Association Classification Class ≥II), life-threatening, uncontrolled arrhythmia, cerebrovascular accident, or transient ischemic attack.

10. QTc >470 msec using the Fridericia Formula.

11. History of a complete bundle branch block or high-degree atrioventricular block.

12. History of or any concurrent condition, therapy, or laboratory abnormality that in the Investigator's opinion might confound the results of the study, interfere with the patient's participation for the full duration of the study, or is not in the best interest of the patient to participate.

13. Clinically active central nervous system (CNS) leukemia.

14. Patients on immunosuppressive therapy post-HSCT at the time of screening with R/R leukemia (must be off all systemic immunosuppression therapy for at least 2 weeks and calcineurin inhibitors for at least 4 weeks). The use of topical steroids for cutaneous graftversus- host disease (GVHD) or stable systemic steroid doses less than or equal to 20 mg of prednisone daily are permitted.

15. Patients with Grade > 2 active acute GVHD, moderate or severe limited chronic GVHD, or extensive chronic GVHD of any severity.

• Minimum Eligible Age: 12 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Astex Pharmaceuticals, Inc.

INDUSTRY

Sponsor Role: collaborator

Syndax Pharmaceuticals

INDUSTRY

Sponsor Role: collaborator

M.D. Anderson Cancer Center

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Ghayas Issa, MD

Role: PRINCIPAL_INVESTIGATOR

M.D. Anderson Cancer Center

Locations

M D Anderson Cancer Center

Houston, Texas, United States

Site Status: RECRUITING

Countries

United States

Central Contacts

Ghayas Issa, MD

Role: CONTACT

gcissa@mdanderson.org

(713) 745-6798

Facility Contacts

Ghayas Issa, MD

Role: primary

gcissa@mdanderson.org

713-745-6798

Provided Documents

Document Type: Informed Consent Form

View Document

Related Links

http://www.mdanderson.org

M D Anderson Cancer Center

Other Identifiers

NCI-2022-03312

Identifier Type: OTHER

Identifier Source: secondary_id

2021-1059

Identifier Type: -

Identifier Source: org_study_id