GLP-1 RA Plus SOC Treatment in First-line, Metastatic Pancreatic, Colorectal, or Hepatocellular Cancer
NCT07627191 · Not yet recruiting
Last updated 2026-07-13This clinical trial is testing the safety of adding a GLP-1 receptor agonist (GLP-1 RA) to standard chemotherapy in people with newly diagnosed metastatic pancreatic, colorectal, or liver cancer.
What this study is testing ClinicalTrials.gov NCT07627191 ↗
Description as written by the study sponsor.
There is a growing number of patients diagnosed with gastrointestinal cancers who are also simultaneously being treated with GLP-1 Receptor Agonists (RA)s. To date, no clinical trial data exists to establish safety and/or feasibility with use of GLP-1 RAs during chemotherapy in the metastatic setting. The goal of this clinical trial is to evaluate the safety, tolerability, preliminary efficacy, and correlative analyses of combining GLP-1 RAs with standard chemotherapy in patients with metastatic pancreatic, colorectal, or hepatocellular cancers in the first-line setting.
Treatments tested
- GLP1-RA (semaglutide) Drug
Patients will receive 6 months of weekly semaglutide; weekly subcutaneous injection; dose escalation will occur every 4 weeks with dose titration as follows: 0.25 mg → 0.5 mg → 1 mg → 1.7 mg → Maintenance at 2.4 mg or 1.7 mg pending tolerability.
| Main thing measured | Incidence of Treatment Emergent Adverse Events [Safety] attributed to GLP1-RA and/or its interaction with chemotherapy |
|---|---|
| Sponsor | University of Arizona |
| Conditions studied | Pancreatic Cancer, Colorectal Cancer, Hepatocellular Carcinoma |
| GLP-1 drugs | — |
Full protocol, eligibility, and contacts on ClinicalTrials.gov NCT07627191 ↗