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.

Stopped early · Phase 2

Conditions studied: Non-small Cell Lung Cancer

In brief

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.

Key facts

Study ID
NCT03968419
Run by
Novartis Pharmaceuticals
People needed
88
Starts
2019-11-05
Expected to finish
2022-08-15
Last updated by the study team
2024-06-20

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

Where it is running

Full record on ClinicalTrials.gov

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