Studying TAK-243 in Patients With Advanced Cancer
NCT06223542 · Status: RECRUITING · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 95
Last updated 2026-05-13
Summary
This phase I trial studies the side effects and best dose of ubiquitin-activating enzyme (UAE) inhibitor TAK-243 (TAK-243) in treating patients with a solid tumor that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced) or that has spread from where it first started (primary site) to other places in the body (metastatic) and in patients with lymphoma. TAK-243 is a drug that binds to and inhibits the ubiquitin-activating enzyme, an enzyme that is more active on cancer cells than healthy cells, inhibiting tumor cell proliferation and survival.
Conditions
- Advanced Lymphoma
- Advanced Malignant Solid Neoplasm
- Indolent Non-Hodgkin Lymphoma
- Metastatic Malignant Solid Neoplasm
- Recurrent Malignant Solid Neoplasm
- Refractory Malignant Solid Neoplasm
Interventions
- PROCEDURE
-
Biopsy Procedure
Undergo biopsy
- PROCEDURE
-
Biospecimen Collection
Undergo collection of blood
- PROCEDURE
-
Computed Tomography
Undergo CT
- PROCEDURE
-
Echocardiography Test
Undergo ECHO
- PROCEDURE
-
Magnetic Resonance Imaging
Undergo MRI
- DRUG
-
UAE Inhibitor TAK-243
Given IV
Sponsors & Collaborators
-
National Cancer Institute (NCI)
lead NIH
Principal Investigators
-
Sarah Shin, MD · National Cancer Institute LAO
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2025-03-24
- Primary Completion
- 2027-04-15
- Completion
- 2027-04-15
- FDA Drug
- Yes
Countries
- United States
Study Locations
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