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.

NCT03968419

Phase 2 Terminated 88 enrolled Novartis Pharmaceuticals
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

EvaluationDrugModalityDoseRoute
Subject Canakinumab Monoclonal antibody 200 mg Subcutaneous
Subject Pembrolizumab Monoclonal antibody 200 mg Other