PDR001 in Combination With Platinum-doublet Chemotherapy and Other Immunology Agents in PD-L1 Unselected, Metastatic NSCLC Patients

Stopped early · Phase 1

Conditions studied: Non-small Cell Lung Cancer

In brief

The primary purpose of this study is to establish the maximum tolerated dose (MTD) and/or recommended dose for expansion (RDE) of PDR001 when administered in combination with platinum-doublet chemotherapy and other immunooncology agent(s) in treatment naive patients with PD-L1 unselected, advanced NSCLC, and to estimate the preliminary anti-tumor activity in this patient population.

Key facts

Study ID
NCT03064854
Run by
Novartis Pharmaceuticals
People needed
111
Starts
2017-05-24
Expected to finish
2021-07-28
Last updated by the study team
2022-08-15

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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