drugset / Trial / NCT03628521

First-line Combination Treatment Based on Anlotinib

NCT03628521

Phase 1 Unknown 80 enrolled Shanghai Chest Hospital
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The aim of this study is to explore safety and therapeutic efficacy of anlotinib combined with erlotinib/chemotherapy/IBI308 as first-line treatment in advanced NSCLC patients. The primary endpoints of the study are safety and objective response rate (ORR);the secondary endpoints are disease control rate (DCR), progression-free survival (PFS) and overall survival (OS).

Timeline

Start
2018-07-20
Primary completion
2019-12-31
Completion
2020-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Carboplatin Small molecule 5 unknown Intravenous
Subject Catequentinib Small molecule 10 mg
Subject Catequentinib Small molecule 12 mg
Subject Erlotinib Small molecule 150 mg
Subject Gemcitabine Small molecule 1000 mg/m2 Intravenous
Subject Pemetrexed Small molecule 500 mg/m2 Intravenous
Subject Sintilimab Monoclonal antibody 200 mg Intravenous

Indications