A PHASE 1/2, OPEN-LABEL, MULTICENTER STUDY OF ORAL MRT-2359 INPATIENTS WITH MYC-DRIVEN AND OTHER SELECTED SOLID TUMORSINCLUDING LUNG CANCER AND DIFFUSE LARGE B-CELL LYMPHOMA
Study of MRT-2359 in Patients with Solid Tumors
Sponsor: Monte Rosa Therapeutics
Enrolling: Male and Female Patients
IRB Number: AAAU6158
U.S. Govt. ID: NCT05546268
Contact: Research Nurse Navigator: 212-342-5162 / cancerclinicaltrials@cumc.columbia.edu
Additional Study Information: The purpose of this study is to evaluate the safety and confirm the best dose in humans for an investigational drug called MRT-2359 in subjects with solid tumors and diffuse large B-cell lymphoma. Investigational means the study drug has not been approved for the treatment of participants with cancer by the Food and Drug Administration (FDA) or any other health/regulatory authority anywhere in the world.MRT-2359 is called a molecular glue degrader or MGD. This MGD can selectively stick to a protein called G1 To S Phase Transition 1 (GSPT1) and cause GSPT1 to breakdown within the cancer cell. The GSPT1 protein is part of an internal cellular process which helps cancer cells to grow rapidly. MRT-2359 may help decrease the number of cancer cells in your body by targeting and destroying the GSPT1 protein and leading to cancer cell death. This is the first time that MRT-2359 is being given to humans. Cancer include: bladder cancer, breast cancer, colon and rectal cancer, esophageal cancer, gynecologic cancers, kidney cancer, lung cancer, Non-Hodgkin's lymphoma, pancreatic cancer, prostate cancer, stomach cancer, testicular cancer, and thyroid cancer.
Investigator
Benjamin Herzberg, MD
Do You Qualify?
Are you at least 18 years old? Yes No
Is your life expectancy greater than 3 months? Yes No
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For more information, please contact:
Research Nurse Navigator
cancerclinicaltrials@cumc.columbia.edu
212-342-5162