drugset / Trial / NCT02826837

LEAC-102 for Advanced Colorectal Cancer

NCT02826837

Phase 1/2 Unknown 30 enrolled Taiwan Leader Biotech Corp.
NaSingle-groupOpen-labelTreatment

Summary

A Phase I/IIa Dose-Escalation Study Evaluating the Safety, Tolerability and Efficacy of LEAC-102 in Combination with FOLFOX + Bevacizumab/Cetuximab in Subjects with Advanced Colorectal Cancer

Timeline

Start
2022-09-01
Primary completion
2024-02-01
Completion
2024-02-01

Drugs

EvaluationDrugModalityDoseRoute
Subject LEAC-102 Unknown 1500 mg Oral
Subject LEAC-102 Unknown 2000 mg Oral
Subject LEAC-102 Unknown 2500 mg Oral
Background Bevacizumab Monoclonal antibody Intravenous
Background Cetuximab Monoclonal antibody Intravenous
Background Leucovorin Small molecule Intravenous
Background Oxaliplatin Small molecule Intravenous
Background fluorouracil Small molecule Intravenous

Indications