HomeTrialNCT07517198
🔬NCT07517198Phase 1RECRUITING

Dose Determining Study of EXS74539 (REC-4539) in Participants With Select Solid Tumors

Study 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.

Interventions / Drugs
View on ClinicalTrials.gov ↗
Study Details
Enrollment40 participants
Primary Completion
Lead SponsorExscientia AI Ltd., a wholly owned subsidiary of Recursion Pharmaceuticals, Inc.
Data Retrieved2026-04-11 04:26:31.746388+00:00
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