Trials / Unknown
UnknownNCT04211896
Anlotinib Combined With Nivolumab for Non-Small Cell Lung Cancer
The Efficacy and Safety of Anlotinib Combined With Nivolumab as a Second-Line Treatment in Patients With Advanced Non-Small Cell Lung Cancer
- Status
- Unknown
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 70 (estimated)
- Sponsor
- The First Affiliated Hospital with Nanjing Medical University · Academic / Other
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
This study evaluates the safety and efficacy of anlotinib in combination with nivilumab as second-line treatment in advanced NSCLC patients. The primary endpoint of the study is progression-free survival (PFS);the secondary endpoints are disease control rate (DCR), objective response rate (ORR), overall survival (OS) and safety.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Anlotinib | Anlotinib will be given at a dose of 12mg once daily on days 1-14 of a 21-day cycle. |
| DRUG | Nivolumab | Nivolumab will be given at a dose of 240 mg every 2 weeks (Odd Cycles: Days 1 and 15 and Even Cycles Day 8) per 21 day Cycle. |
Timeline
- Start date
- 2020-01-01
- Primary completion
- 2021-07-01
- Completion
- 2022-01-01
- First posted
- 2019-12-26
- Last updated
- 2019-12-26
Source: ClinicalTrials.gov record NCT04211896. Inclusion in this directory is not an endorsement.