Phase 1 Study of Venetoclax/Azacitidine or Venetoclax in Combination With Ziftomenib or Standard Induction Cytarabine/Daunorubicin (7+3) Chemotherapy in Combination With Ziftomenib for the Treatment of Patients With Acute Myeloid Leukemia

Status: Recruiting
Location: See all (44) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

Ziftomenib is an investigational drug in development for the treatment of patients with acute myeloid leukemia (AML) with certain genetic alterations. This protocol has 3 separate arms that will investigate the benefits and risks of adding ziftomenib to standard-of-care (SOC) drug treatments in patients who have AML with certain genetic mutations. Both newly diagnosed and relapsed refractory patients with AML will be assigned to different cohorts based on specific study criteria and physician discretion. The purpose of this study is to assess the safety, tolerability, and early signs of efficacy of ziftomenib in combination with SOC drugs to treat AML.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients must have a documented NPM1 mutation or KMT2A rearrangement and have either newly diagnosed or relapsed/refractory AML

⁃ Those intending treatment with intensive chemotherapy in Arm C should be NPM1-m and FLT3-ITD+ with an allelic ratio ≥0.05 and eligible for FLT3-targeted treatment

• Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2

• Adequate liver, renal, and cardiac function according to protocol defined criteria

• A female of childbearing potential must agree to use adequate contraception as well as a double barrier method from the time of screening through 180 days following the last dose of study intervention. A male of childbearing potential must agree to use abstinence or use a double barrier method of contraception from the time of screening through 180 days following the last dose of study intervention

⁃ Female patients of childbearing potential who receive quizartinib in Arm C should use a highly effective method of contraception during quizartinib treatment and for 7 months after the last dose

Locations
United States
Arizona
Mayo Clinic - Phoenix
RECRUITING
Phoenix
California
Moores UC San Diego Cancer Center
RECRUITING
La Jolla
UCLA - Bowyer Oncology Center
RECRUITING
Los Angeles
USC / Norris Comprehensive Cancer Center
RECRUITING
Los Angeles
UC Irvine Health Chao Family Comprehensive Cancer Center
RECRUITING
Orange
Colorado
University of Colorado
RECRUITING
Aurora
Colorado Blood Cancer Institute
RECRUITING
Denver
Connecticut
Yale Cancer Center and Smilow Cancer Hospital
RECRUITING
New Haven
Florida
Mayo Clinic Jacksonville
RECRUITING
Jacksonville
Georgia
Emory Healthcare - The Emory Clinic
RECRUITING
Atlanta
Georgia Cancer Center at Augusta University
RECRUITING
Augusta
Iowa
University of Iowa Hospitals & Clinics
RECRUITING
Iowa City
Illinois
Robert H. Lurie Comprehensive Cancer Center of Northwestern University
RECRUITING
Chicago
Loyola University Medical Center
RECRUITING
Maywood
Kansas
The University of Kansas Medical Center Research Institute
RECRUITING
Fairway
Kentucky
Norton Cancer Institute - St. Matthews
RECRUITING
Louisville
University of Kentucky Markey Cancer Center
RECRUITING
Louisville
Louisiana
Ochsner MD Anderson Cancer Center
RECRUITING
Jefferson
Massachusetts
Massachusetts General Hospital
RECRUITING
Boston
UMass Chan Medical School
RECRUITING
Worcester
Maryland
Johns Hopkins School of Medicine
RECRUITING
Baltimore
Michigan
University of Michigan Comprehensive Cancer Center
RECRUITING
Ann Arbor
Karmanos Cancer Institute
RECRUITING
Detroit
Minnesota
University of Minnesota
RECRUITING
Minneapolis
Mayo Clinic - Rochester
RECRUITING
Rochester
North Carolina
Duke Blood Cancer Center
RECRUITING
Durham
New Jersey
Hackensack University Medical Center
RECRUITING
Hackensack
Rutgers Cancer Institute
RECRUITING
New Brunswick
New York
Roswell Park Comprehensive Cancer Center
RECRUITING
Buffalo
Columbia University Medical Center
RECRUITING
New York
Mount Sinai - Ruttenberg Treatment Center
RECRUITING
New York
New York - Presbyterian / Weill Cornell Medicine
RECRUITING
New York
Stony Brook University Hospital
RECRUITING
Stony Brook
Ohio
Cleveland Clinic Taussig Cancer Institute
RECRUITING
Cleveland
University Hospitals Cleveland Medical Center
RECRUITING
Cleveland
The James Cancer Hospital and Solove Research Institute
RECRUITING
Columbus
Oklahoma
OU Health Stephenson Cancer Center
RECRUITING
Oklahoma City
Pennsylvania
Hospital of the University of Pennsylvania
RECRUITING
Philadelphia
Tennessee
TriStar Bone Marrow Transplant
RECRUITING
Nashville
Texas
Sarah Cannon Research Institute - St. David's South Austin Medical Center / Texas Oncology South Austin
RECRUITING
Austin
UT Southwestern - Simmons Cancer Center
RECRUITING
Dallas
MD Anderson Cancer Center
RECRUITING
Houston
Wisconsin
University of Wisconsin Hospital and Clinics
RECRUITING
Madison
Medical College of Wisconsin Cancer Center
RECRUITING
Milwaukee
Contact Information
Primary
Clinical Operations
KO-MEN-007@kuraoncology.com
617-588-3755
Time Frame
Start Date: 2023-07-18
Estimated Completion Date: 2030-04
Participants
Target number of participants: 420
Treatments
Experimental: Dose Escalation: Ziftomenib with Venetoclax and Azacitidine in R/R NPM1-m (A-1)
Ziftomenib with Venetoclax and Azacitidine in relapsed/refractory NPM1-m AML patients who have failed at least one prior line of therapy
Experimental: Dose Validation/Expansion: Ziftomenib with Venetoclax and Azacitidine in R/R NPM1-m (A-1)
Ziftomenib with Venetoclax and Azacitidine in relapsed/refractory NPM1-m AML patients who have failed at least one prior line of therapy
Experimental: Dose Escalation: Ziftomenib with 7+3 in 1L NPM1-m/FLT3 wildtype (A-2)
Ziftomenib with 7+3 in newly diagnosed NPM1-m AML patients who are candidates for intensive chemotherapy and must be FLT3 wildtype or ITD ratio \<0.05
Experimental: Dose Validation/Expansion: Ziftomenib with 7+3 in 1L NPM1-m/FLT3 wildtype (A-2)
Ziftomenib with 7+3 in newly diagnosed NPM1-m AML patients who are candidates for intensive chemotherapy and must be FLT3 wildtype or ITD ratio \<0.05
Experimental: Dose Validation/Expansion: Ziftomenib with Venetoclax in R/R NPM1-m (A-3)
Ziftomenib with Venetoclax in relapsed/refractory NPM1-m AML patients who have failed at least one prior line of therapy
Experimental: Dose Validation/Expansion: Ziftomenib with Venetoclax and Azacitidine in 1L NPM1-m (A-4)
Ziftomenib with Venetoclax and Azacitidine in newly diagnosed NPM1-m AML patients
Experimental: Dose Escalation: Ziftomenib with Venetoclax and Azacitidine in R/R KMT2A-r (B-1)
Ziftomenib with Venetoclax and Azacitidine in relapsed/refractory KMT2A-r AML patients who have failed at least one prior line of therapy
Experimental: Dose Validation/Expansion: Ziftomenib with Venetoclax and Azacitidine in R/R KMT2A-r (B-1)
Ziftomenib with Venetoclax and Azacitidine in relapsed/refractory KMT2A-r AML patients who have failed at least one prior line of therapy
Experimental: Dose Escalation: Ziftomenib with 7+3 in 1L KMT2A-r (B-2)
Ziftomenib with 7+3 in newly diagnosed KMT2A-r AML patients who are candidates for intensive chemotherapy
Experimental: Dose Validation/Expansion: Ziftomenib with 7+3 in 1L KMT2A-r (B-2)
Ziftomenib with 7+3 in newly diagnosed KMT2A-r AML patients who are candidates for intensive therapy
Experimental: Dose Validation/Expansion: Ziftomenib with Venetoclax + Azacitidine in 1L KMT2A-r (B-3)
Ziftomenib with Venetoclax and Azacitidine in newly diagnosed KMT2A-r AML patients
Experimental: Dose Escalation: Ziftomenib with 7+3+quizartinib in 1L NPM1-m/FLT3-ITD+ AML patients (C-1)
Ziftomenib with 7+3 and quizartinib in newly diagnosed NPM1-m and FLT3-ITD+ (with allelic ratio ≥0.05) AML patients who are candidates for IC and eligible to receive FLT3-targeted therapy
Experimental: Dose Validation/Expansion: Ziftomenib with 7+3+quizartinib in 1L NPM1-m/FLT3-ITD+ AML patients (C-1)
Ziftomenib with 7+3 and quizartinib in newly diagnosed NPM1-m and FLT3-ITD+ (with allelic ratio ≥0.05) AML patients who are candidates for IC and eligible to receive FLT3-targeted therapy
Sponsors
Leads: Kura Oncology, Inc.

This content was sourced from clinicaltrials.gov