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Clinical Trial Summary

The primary objective of the study is to compare the objective response rate (ORR) of high dose cemiplimab (HDREGN2810) and standard dose cemiplimab plus ipilimumab combination therapy (SDREGN2810/ipi) to the ORR of standard dose cemiplimab (SDREGN2810) in the second-line treatment of patients with advanced squamous or non-squamous non-small cell lung cancer (NSCLC), in patients whose tumors express programmed cell death ligand 1 (PD-L1) in <50% of tumor cells.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03430063
Study type Interventional
Source Regeneron Pharmaceuticals
Contact
Status Terminated
Phase Phase 2
Start date May 29, 2018
Completion date October 27, 2021

See also
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