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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

About this study

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.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take GTAEXS617
  • 2.Take SoC
PhasePhase 1/Phase 2
Primary goalNumber of Participants With Treatment Emergent Adverse Events (TEAEs)

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low10%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

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