Clin2
NCT06951217Possibly a fitRecruiting

Long-term safety study of an inhaled drug for lung scarring

Progressive Pulmonary FibrosisIdiopathic Pulmonary Fibrosis (IPF)

Part of Lungs & breathing clinical trials.

This study continues treatment for people who already completed a previous study with an Avalyn inhaled antifibrotic drug. It aims to check the long-term safety of the medication for patients with certain types of lung scarring.

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

Phase
Phase 2
Enrollment
340 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You must have completed a prior Avalyn study for idiopathic pulmonary fibrosis (IPF) or progressive pulmonary fibrosis (PPF) while on the full dose of the study drug (active or placebo).
  • If you are a man or a woman who can have children, you must agree to use effective birth control during the study and for 90 days after the last dose.
  • You cannot have had a flare-up of asthma or COPD that needed oral or steroid pills in the last 3 months.
  • You cannot have had a sudden worsening of your lung scarring (IPF or PPF) in the last 3 months.
  • You should not be taking any other experimental drugs (except the Avalyn study drug) within the past 30 days or 5 half-lives of that drug, whichever is shorter.
  • You must not have had a severe allergic reaction to pirfenidone or any ingredients in this study drug.

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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