drugset / Trial / NCT04617522

Study of Sacituzumab Govitecan in Participants With Advanced or Metastatic Solid Tumor and Moderate Liver Impairment

NCT04617522

Phase 1 Recruiting 30 enrolled Gilead Sciences
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The goals of this clinical study are to learn more about the safety and dosing of the study drug, sacituzumab govitecan-hziy, in participants with solid tumors and moderate liver problems.

Timeline

Start
2021-04-06
Primary completion
2026-12
Completion
2026-12

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Sacituzumab Govitecan Monoclonal antibody 5 mg/kg Intravenous
Subject Sacituzumab Govitecan Monoclonal antibody 7.5 mg/kg Intravenous
Subject Sacituzumab Govitecan Monoclonal antibody 10 mg/kg Intravenous

Indications