Clin2
NCT06165341Possibly a fitRecruiting

Fazirsiran for mild liver scarring in alpha-1 antitrypsin deficiency

Alpha1-Antitrypsin Deficiency

Part of Digestive system, Genetic & congenital, Lungs & breathing clinical trials.

This study tests an investigational drug called fazirsiran, which is designed to treat alpha-1 antitrypsin deficiency-related liver disease with mild scarring. The goal is to see if fazirsiran is safe and can improve or slow liver damage in people with the PiZZ genetic type.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 3
Enrollment
50 people
Ages
18 years to 75 years
Study type
Interventional

Who can take part

  • You must be between 18 and 75 years old.
  • You must have a specific genetic type of alpha-1 antitrypsin deficiency called PiZZ (confirmed by a blood test or medical records).
  • You must have mild liver scarring (stage F1) seen on a liver biopsy — a new biopsy can be done during the screening process.
  • You cannot have more advanced liver scarring (stage F2 or higher), complications of cirrhosis, or other forms of chronic liver disease.
  • You must not smoke and must not regularly use oxygen therapy (a CPAP for sleep apnea is allowed).
  • You cannot have active infections with hepatitis B, hepatitis C, or HIV.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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