drugset / Trial / NCT05927857

Summary

Primary Objectives * In phase 1b cohort, to determine MTD (maximum tolerated dose) of nal-IRI (ONIVYDE®) in combination with Ramucirumab (Cyramza®) and TAS-102 (LONSURF®) * In phase II cohort, to evaluate disease objective response rate (ORR) of Ramucirumab (Cyramza®), nal-IRI (ONIVYDE®) in combination with TAS-102 (LONSURF®) Secondary Objectives * To evaluate disease control rate (DCR) * To evaluate progression-free survival (PFS) * To evaluate overall survival (OS) * To assess the safety profile * To study the blood biomarkers

Timeline

Start
2024-04-01
Primary completion
2027-12-31
Completion
2028-12-31

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Irinotecan Small molecule 50 mg/m2 Intravenous
Subject Irinotecan Small molecule 60 mg/m2 Intravenous
Subject Irinotecan Small molecule 70 mg/m2 Intravenous
Subject Ramucirumab Monoclonal antibody 8 mg/kg Intravenous
Subject Tipiracil Small molecule Oral
Subject Trifluridine Small molecule Oral