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RECRUITING
NCT07517198
PHASE1

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.

View on ClinicalTrials.gov

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

Interventions

DRUG

EXS74539

Oral administration

Locations (2)

START Dallas

Fort Worth, Texas, United States

START Mountain Region

West Valley City, Utah, United States