Status: Recruiting
Study to Assess GTAEXS617 in Participants With Advanced Solid Tumors
The primary purpose of this study is to assess the safety, tolerability, pharmacokinetics (PK) and anti-tumor activity of GTAEXS617 (REC-617) in participants with advanced solid tumors.
Participants needed: 230
Trial details
Phase: Phase 1, Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Exscientia AI Ltd., a wholly owned subsidiary of Recursion Pharmaceuticals, Inc.Updated: Apr 23, 2026Locations: 13
Eligibility criteria
Eastern Cooperative Oncology Group (ECOG) performance status 0-1. [+5]
Active and clinically significant (CS) infection. [+11]