Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Chronic Obstructive Pulmonary Disease
Type
Interventional
Phase
Phase 3
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)Primary Purpose: Treatment

Participation Requirements

Age
Between 40 years and 85 years
Gender
Both males and females

Description

The study duration per participant is approximatively 76 weeks including a 3-to-5-week screening period, a 52-week treatment period on investigational medicinal product (IMP) and a 20-week post-IMP treatment follow-up period.

The study duration per participant is approximatively 76 weeks including a 3-to-5-week screening period, a 52-week treatment period on investigational medicinal product (IMP) and a 20-week post-IMP treatment follow-up period.

Tracking Information

NCT #
NCT04701983
Collaborators
Regeneron Pharmaceuticals
Investigators
Study Director: Clinical Sciences & Operations Sanofi