155
Participants
Start Date
March 31, 2025
Primary Completion Date
April 30, 2029
Study Completion Date
April 30, 2031
PHST001
"* PHST001 will be administered as IV infusions in a 3-week (Q3W) dosing interval. The dosing day will be on Day 1, 21 days cycle.~* Other Names:~* Dose Level 1~* Dose Level 2~* Dose Level 3~* Dose Level 4~* Dose Level 5~* Dose Level 6~* Dose Level 7~Drug: PHST001~* PHST001 will be administered as IV infusions in a 3-week (Q3W) dosing interval. The dosing day will be on Day 1, 21 days cycle.~This study is an open label, Phase 1 dose escalation trial with three expansion cohorts. The study consists of two parts:~* Part A: Dose escalation in patients with advanced solid tumors. Approximately 40-80 in total will be in enrolled in part A, covering 7 dose level.~* Part B: Expansion cohorts will be added as an amendment as further preclinical data and clinical data from Part A become available."
RECRUITING
Duke Cancer Institute, Durham
NOT_YET_RECRUITING
Vanderbilt-Ingram Cancer Center, Nashville
RECRUITING
University of Michigan Rogel Cancer Center, Ann Arbor
RECRUITING
University of Chicago Medical Center, Chicago
RECRUITING
MD Anderson Cancer Center, Houston
RECRUITING
South Texas Accelerated Research Therapeutics (START), San Antonio
RECRUITING
USC Norris Comprehensive Cancer Center, Los Angeles
RECRUITING
Stanford University School of Medicine, Palo Alto
RECRUITING
Yale Cancer Center, New Haven
RECRUITING
Dana Farber Cancer Institute, Boston
Lead Sponsor
Pheast Therapeutics
INDUSTRY