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