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Clinical trial

A Phase 4, Multicenter, Double-blind, Study to Investigate the Efficacy, Safety, and Tolerability of 3 Active Doses of Respreeza® / Zemaira® Weekly Intravenous Infusions Administered Over 3 Years as Longterm Maintenance Therapy in Adult Subjects With Emphysema Related to Alpha1 Antitrypsin Deficiency

NCT07326592 is registered in ClinicalTrials.gov with CSL Behring as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Phase 4, Multicenter, Double-blind, Study to Investigate the Efficacy, Safety, and Tolerability of 3 Active Doses of Respreeza® / Zemaira® Weekly Intravenous Infusions Administered Over 3 Years as Longterm Maintenance Therapy in Adult Subjects With Emphysema Related to Alpha1 Antitrypsin Deficiency
Lead sponsor
CSL Behring
Phase
Phase 4
Overall status
Not yet recruiting
Start date
July 20, 2026
Completion date
September 15, 2033
Enrollment
270 (estimated)
Sites
Not reported

Conditions

As the registry lists them; a condition with its own page is linked.

alpha1 antitrypsin deficiency, alpha1-proteinase inhibitor deficiency, emphysema