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Study details
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Study to Assess GTAEXS617 in Participants With Advanced Solid Tumors

Exscientia AI Ltd., a wholly owned subsidiary of Recursion Pharmaceuticals, Inc.
NCT IDNCT05985655ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1/2

Target enrollment

165

Study length

about 4.9 years

Ages

18+

Locations

3 sites in MI, TX, UT

What this study is about

This trial is testing a treatment called GTAEXS617 for people with advanced solid tumors. The goal is to see if the treatment is safe and effective.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take GTAEXS617
  • 2.Take SoC

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Primary: Number of Participants With Treatment Emergent Adverse Events (TEAEs), Phase 2 : Objective Response Rate (ORR) as Assessed by Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1

Secondary: Disease Control Rate (DCR), Duration of Response (DOR), Maximum Plasma Concentration (Cmax) of GTAEXS617, Phase 1: ORR as Assessed by Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1, Progression-Free Survival (PFS), Time Maximum Plasma Concentration (Tmax) of GTAEXS617

Body systems

Oncology