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Brief Title: Study of TP-3654 in Patients With Advanced Solid Tumors
Official Title: A Phase I, First-in-human, Open-label, Dose Escalation, Safety, Pharmacokinetic, and Pharmacodynamic Study of Oral TP-3654 in Patients With Advanced Solid Tumors
Study ID: NCT03715504
Brief Summary: TP-3654 is an oral PIM inhibitor. This is a Phase 1, open-label, dose-escalation, safety, pharmacokinetics, and pharmacodynamic study, with a purpose of determining the maximum tolerated dose (MTD) and dose-limiting toxicities (DLTs) of oral TP-3654 in patients with advanced solid tumors.
Detailed Description: Primary Objective: ⢠To determine the maximum tolerated dose (MTD) and dose-limiting toxicities (DLTs) of oral TP-3654 in patients with advanced solid tumors. Secondary Objectives: * To establish the pharmacokinetic (PK) profile of orally administered TP-3654 * To observe patients for any evidence of antitumor activity of TP-3654 by objective radiographic assessment * To study the pharmacodynamic effects of TP-3654 therapy * To establish the Recommended Phase 2 Dose (RP2D) for future studies with TP-3654
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
MD Anderson, Houston, Texas, United States
Huntsman Cancer Institute, Salt Lake City, Utah, United States
University of Virginia, Charlottesville, Virginia, United States
Name: Sumitomo Dainippon Pharma Oncology, MD
Affiliation: Sumitomo Pharma America, Inc.
Role: STUDY_DIRECTOR