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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
Completion Date
2029-03
Last Updated
2026-04-08
Healthy Volunteers
No
Conditions
Interventions
EXS74539
Oral administration
Locations (2)
START Dallas
Fort Worth, Texas, United States
START Mountain Region
West Valley City, Utah, United States