Study on GTAEXS617 for Adults with Advanced Solid Tumors
Sponsor: Exscientia AI Ltd., a wholly owned subsidiary of Recursion Pharmaceuticals, Inc.
Sponsor score: 0
ClinicalTrials ID:NCT05985655
This clinical trial is testing a new drug, GTAEXS617, to see if it is safe and effective in treating adults with advanced solid tumors. The study will also look at how the drug moves through the body and its effects on tumors.
Patient Parameters
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Program Overview
The main goal of this study is to find out if the new drug GTAEXS617 is safe and well-tolerated in adults with advanced solid tumors. Researchers will also study how the drug is processed in the body and its potential to reduce tumor size.
Eligibility Criteria
Inclusion Criteria
- Be in good overall health with an ECOG performance status of 0 or 1, meaning fully active or restricted in physically strenuous activity but ambulatory.
- Have a life expectancy of more than 3 months.
- Have one of the following confirmed advanced solid tumors: head and neck cancer, pancreatic cancer, non-small cell lung cancer, hormone receptor-positive and HER2-negative breast cancer that has worsened after previous treatment, or certain types of ovarian, peritoneal, or fallopian tube cancers that are resistant to platinum-based treatments.
- The cancer must be advanced, recurrent, or metastatic, meaning it cannot be cured with surgery or radiation.
- Have good blood, liver, and kidney function.
- Have tumors that can be biopsied, except for bone metastases.
Exclusion Criteria
- Have an active and significant infection.
- Have severe nausea, vomiting, or digestive issues that affect drug absorption.
- Have cancer that has spread to the brain or spinal cord and is causing symptoms.
- Have another active or previous cancer.
- Have had an organ or stem-cell transplant.
- Have moderate or severe heart disease.
- Have received cancer treatment within 28 days or 5 half-lives before starting the study drug.
- Have taken certain medications that affect how the body processes drugs within 14 days or 5 half-lives before starting the study drug.
- Have unresolved serious side effects from previous cancer treatments.
- Have had major surgery less than 28 days before starting the study drug.
Locations
| FACILITY | ZIP | CITY | STATE |
|---|---|---|---|
| START Midwest | 49546 | Grand Rapids | Michigan |
| START San Antonio | 78229 | San Antonio | Texas |
| START Mountain Region | 84119 | West Valley City | Utah |
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