This is a multi-center, randomized, placebo-controlled, double blind clinical study to assess the efficacy and safety of two separate dose regimens of Alpha-1 MP versus placebo for 156 weeks (i.e., 3 years) using computed tomography (CT) of the lungs as the main measure of efficacy. The two Alpha-1 MP doses to be tested are 60 mg/kg and 120 mg/kg administered weekly by IV infusion for 156 weeks. The study consists of an optional pre-screening phase, Screening Phase, a 156-week Treatment Phase, and an End of Study Visit at Week 160.
| Facility | City | Region | Status |
|---|---|---|---|
| Grifols Investigative Site | Phoenix | Arizona | |
| Grifols Investigative Site | Gainesville | Florida | |
| Grifols Investigative Site | Leesburg | Florida | |
| Grifols Investigative Site | Miami | Florida | |
| Grifols Investigative Site | St Louis | Missouri | |
| Grifols Investigative Site | Wilmington | North Carolina | |
| Grifols Investigative Site | Portland | Oregon | |
| Grifols Investigative Site | Hershey | Pennsylvania | |
| Grifols Investigative Site | Charleston | South Carolina | |
| Grifols Investigative Site | Tyler | Texas | |
| Grifols Investigative Site | Vicente López | Buenos Aires | |
| Grifols Investigative Site | Córdoba | Córdoba Province | |
| Grifols Investigative Site | Sydney | New South Wales | |
| Grifols Investigative Site | Chermside | Queensland | |
| Grifols Investigative Site | Adelaide | South Australia | |
| Grifols Investigative Site | Fitzroy | Victoria | |
| Grifols Investigative Site | Nedlands | Western Australia | |
| Grifols Investigative Site | Santo André | São Paulo | |
| Grifols Investigative Site | São Paulo | São Paulo | |
| Grifols Investigative Site | São Paulo | São Paulo | |
| Grifols Investigative Site | St. John's | Newfoundland and Labrador | |
| Grifols Investigative Site | Halifax | Nova Scotia | |
| Grifols Investigative Site | Toronto | Ontario | |
| Grifols Investigative Site | Arhus C | Denmark | |
| Grifols Investigative Site | Hellerup | Denmark | |
| Grifols Investigative Site | Tallinn | Estonia | |
| Grifols Investigative Site | Tartu | Estonia | |
| Grifols Investigative Site | Turku | Finland | |
| Grifols Investigative Site | Pessac | Gironde | |
| Grifols Investigative Site | Bron | Rhone | |
| Grifols Investigative Site | Heidelberg | Baden-Wurttemberg | |
| Grifols Investigative Site | Marburg | Hesse | |
| Grifols Investigative Site | Essen | North Rhine-Westphalia | |
| Grifols Investigative Site | Homburg Saar | Germany | |
| Grifols Investigative Site | Chisinau | Moldova | |
| Grifols Investigative Site | Auckland | New Zealand | |
| Grifols Investigative Site | Christchurch | New Zealand | |
| Grifols Investigative Site | Hamilton | New Zealand | |
| Grifols Investigative Site | Krakow | Poland | |
| Grifols Investigative Site | Warsaw | Poland |
+ 12 more sites — see the full list on the official registry below.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT01983241 on ClinicalTrials.gov ↗ ← All trials in Canada