drugset / Trial / NCT03968419
This Study Will Evaluate the Effect of Canakinumab or Pembrolizumab Given as Monotherapy or in Combination as Neo-adjuvant Treatment for Subjects With Early Stages NSCLC.
RandomizedParallel-groupOpen-labelTreatment
Summary
The purpose of this study was to evaluate the major pathological response (MPR) rate of canakinumab given as a neoadjuvant treatment, either as single agent or in combination with pembrolizumab, in addition to evaluate the MPR of pembrolizumab as a single agent and the dynamic of the tumor microenvironment changes on treatment.
Timeline
- Start
- 2019-11-05
- Primary completion
- 2022-04-20
- Completion
- 2022-08-15
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Canakinumab | Monoclonal antibody | 200 mg | Subcutaneous |
| Subject | Pembrolizumab | Monoclonal antibody | 200 mg | Other |