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8400073","Evanston","60201",{"type":111,"coordinates":337},[338,339],-87.69006,42.04114,{"lat":339,"lon":338},{"facility":342,"status":104,"city":343,"state":344,"zip":345,"country":108,"countryCode":109,"cosmosGeoPoint":346,"geoPoint":350,"contacts":25},"Indy Clinical Research- Site Number : 8400071","Indianapolis","Indiana","46268",{"type":111,"coordinates":347},[348,349],-86.15804,39.76838,{"lat":349,"lon":348},{"facility":352,"status":104,"city":353,"state":354,"zip":355,"country":108,"countryCode":109,"cosmosGeoPoint":356,"geoPoint":360,"contacts":25},"University of Kansas Medical Center- Site Number : 8400054","Kansas City","Kansas","66160",{"type":111,"coordinates":357},[358,359],-94.62746,39.11417,{"lat":359,"lon":358},{"facility":362,"status":104,"city":363,"state":364,"zip":365,"country":108,"countryCode":109,"cosmosGeoPoint":366,"geoPoint":370,"contacts":25},"Southern Clinical Research - Zachary- Site Number : 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are excluded from the study if any of the following criteria apply:\n\n* Asthma, including pediatric asthma, or asthma-COPD overlap syndrome (ACOS)\n* Significant pulmonary disease other than COPD\n* Long-term oxygen therapy \\>4.0 L\u002Fmin or requirement of \\>2.0 L\u002Fmin to maintain oxygen saturation \\>88% at rest\n* Unstable disorder that can impact participants safety or study outcomes\n* Active or incompletely treated tuberculosis\n* Current or past malignancies\n* Concomitant therapies:\n\n  * long-term macrolides or phosphodiesterase Type 3 (PDE-3) or PDE-4 inhibitors unless on stable therapy for \\>6 months\n  * any biologic therapy or systemic immunosuppressant within 4 months or 5 half-lives prior to Screening\n\nThe above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial","ALL","40 Years","80 Years",{"count":2059,"type":2060},942,"ESTIMATED","INTERVENTIONAL",[2063],"PHASE3","This is a parallel, 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