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About
This is a parallel, double blind, Phase 3, 2-arm study that is designed to provide additional safety information, assess the durability of treatment response, and provide additional PK and immunogenicity assessments.
The primary purpose of this study is to evaluate safety and tolerability of both itepekimab SC Q2W or itepekimab SC Q4W in participants with COPD having completed the treatment period of the clinical studies EFC16750 or EFC16819. A secondary purpose of this study is to provide efficacy outcomes beyond the treatment period of the parent trials EFC16750 and EFC16819.
Study details include:
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The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
Primary purpose
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Interventional model
Masking
700 participants in 2 patient groups
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Trial Transparency email recommended (Toll free for US & Canada)
Data sourced from clinicaltrials.gov
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