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A Clinical Study of MK-4208/TERN-701 in Participants With Chronic Myeloid Leukemia (CML) (MK-4208-003/Tern701-1012/CARDINAL)
Trial Status: active
Researchers are looking for a new way to treat a blood cancer called chronic myeloid
leukemia (CML). Researchers want to learn if MK-4208 (Tern-701) can treat this type of
blood cancer.
The goal of this study is to learn about the safety of different doses (amounts) of
MK-4208 (Tern-701) and if people tolerate them. Researchers also want to find the highest
dose of MK-4208 (Tern-701) that people can tolerate and may work to treat blood cancer.
Inclusion Criteria
Key Inclusion Criteria:
Inclusion Criteria include but are not limited to:
- Have an Eastern Cooperative Oncology Group (ECOG) performance status score of 0 to 2
- Have an established cytopathologically confirmed diagnosis of breakpoint cluster
region::Abelson (BCR-ABL1) positive Chronic Myeloid Leukemia (CML) in Chronic Phase
- Have received treatment with at least one prior tyrosine kinase inhibitor (TKI) and
have treatment failure, suboptimal response, or treatment intolerance
- Prior treatment with asciminib is allowed
- Adequate organ function, as assessed by local laboratory
Key Exclusion Criteria:
Exclusion criteria include but are not limited to:
- Systemic antineoplastic therapy (including prior TKIs, interferon-alfa, therapeutic
antibodies, chemotherapy) or other experimental therapy 7 days before the first dose
of MK-4208/TERN-701
- Have completed previous anticancer therapy without resolution of all associated
clinically significant toxicity (to ≤ Grade 2 or baseline)
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT06163430.
Locations matching your search criteria
United States
Alabama
Birmingham
University of Alabama at Birmingham Cancer Center
Status: Active
Name Not Available
California
Orange
UC Irvine Health/Chao Family Comprehensive Cancer Center
Status: Active
Name Not Available
New Jersey
Cherry Hill
Jefferson Cherry Hill Hospital
Status: Active
Name Not Available
New York
New York
Memorial Sloan Kettering Cancer Center
Status: Active
Name Not Available
North Carolina
Charlotte
Carolinas Medical Center/Levine Cancer Institute
Status: Active
Name Not Available
Ohio
Columbus
Ohio State University Comprehensive Cancer Center
Status: Active
Name Not Available
Oregon
Portland
OHSU Knight Cancer Institute
Status: Active
Name Not Available
Pennsylvania
Philadelphia
Thomas Jefferson University Hospital
Status: Active
Name Not Available
Texas
Houston
UT MD Anderson Cancer Center
Status: Active
Name Not Available
Utah
Salt Lake City
Huntsman Cancer Institute/University of Utah
Status: Active
Name Not Available
Washington
Seattle
Fred Hutch/University of Washington/Seattle Children's Cancer Consortium
Status: Active
Name Not Available
Trial PhasePhase I/II
Trial Typetreatment
Lead OrganizationTerns, Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)