Skip to main content
OpenTrials

Clinical trial condition

Pi*ZZ, Pi*SZ, Pi*Null, Another Rare Phenotype/Genotype Known to be Associated With Either Low or Functionally Impaired AAT Including F or I Mutations

Explore clinical trials studying Pi*ZZ, Pi*SZ, Pi*Null, Another Rare Phenotype/Genotype Known to be Associated With Either Low or Functionally Impaired AAT Including F or I Mutations. Study availability and eligibility vary by location and protocol.

1 public trial 0 recruiting studies
Refine in advanced search Browse all conditions

Pi*ZZ, Pi*SZ, Pi*Null, Another Rare Phenotype/Genotype Known to be Associated With Either Low or Functionally Impaired AAT Including F or I Mutations trial results

Completed

Alvelestat (MPH966) for the Treatment of ALpha-1 ANTitrypsin Deficiency

NCT03679598

Conditions
Alpha-1 Antitrypsin Deficiency (AATD), Chronic Disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +15 more
Locations
  • The University of Alabama at Birmingham Lung Health Center Birmingham, Alabama, United States
  • UCLA Los Angeles, California, United States
  • National Jewish Health Denver, Colorado, United States
  • Columbia University New York, United States
View Trial Details

Related conditions