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Clinical Trial Summary

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.


Clinical Trial Description

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Study Design


Related Conditions & MeSH terms


NCT number NCT01983241
Study type Interventional
Source Grifols Therapeutics LLC
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Status Active, not recruiting
Phase Phase 3
Start date November 2013
Completion date January 2027