drugset / Trial / NCT06065371

Sacituzumab Govitecan in Combination With Capecitabine for Advanced Gastrointestinal Cancers After Progression on Standard Therapy

NCT06065371

Phase 1 Recruiting 20 enrolled Henry Ford Health System Gilead Sciences · collab
NaSingle-groupOpen-labelTreatment

Summary

This is a Phase I study to evaluate the safety and tolerability of sacituzumab govitecan in combination with capecitabine for advanced gastrointestinal cancers after progression on standard therapy, and to assess correlation of outcomes with the biomarker Trop-2.

Timeline

Start
2024-11-20
Primary completion
2026-12
Completion
2027-05

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Capecitabine Small molecule 500 mg/m2 Oral
Subject Capecitabine Small molecule 825 mg/m2 Oral
Subject Sacituzumab Govitecan Monoclonal antibody 7.5 mg/kg Intravenous
Subject Sacituzumab Govitecan Monoclonal antibody 10 mg/kg Intravenous