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Dose Determining Study of EXS74539 (REC-4539) in Participants With Select Solid Tumors
Sponsor: Exscientia AI Ltd., a wholly owned subsidiary of Recursion Pharmaceuticals, Inc.
Summary
The primary purpose of this study is to determine the safety, tolerability, and maximum tolerated dose (MTD) of EXS74539 (REC-4539) in participants with select solid tumors.
Official title: A Phase 1, Multicenter, Open-Label, Dose-Escalation Study to Assess Safety, Tolerability, and Efficacy of EXS74539 as Monotherapy in Participants With Select Solid Tumors
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
40
Start Date
2026-04-13
Completion Date
2029-03
Last Updated
2026-06-10
Healthy Volunteers
No
Conditions
Interventions
EXS74539
Oral administration
Locations (3)
Start Lacn
Los Angeles, California, United States
START Dallas
Fort Worth, Texas, United States
START Mountain Region
West Valley City, Utah, United States