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RecruitingSolid TumorSmall Cell Lung Cancer (SCLC)High Grade Neuroendocrine Cancer

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

Eligible age

18+ yrs

Accepts

All genders

Locations

3 states

Healthy volunteers

No

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About this study

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.

Sponsor: Exscientia AI Ltd., a wholly owned subsidiary of Recursion Pharmaceuticals, Inc.

Where it's recruiting

California

Los Angeles

Texas

Fort Worth

Utah

West Valley City

Source: ClinicalTrials.gov · NCT07517198 · last updated 2026-06-10

Dose Determining Study of EXS74539 (REC-4539) in Participants With Sel · TrialPath