drugset / Trial / NCT03628521
First-line Combination Treatment Based on Anlotinib
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |