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NCT05139719Possibly a fitRecruiting

HEC585 trial for slowing lung scarring decline

Progressive Fibrosing Interstitial Lung Disease (PF-ILD) / Progressive Pulmonary Fibrosis (PPF)

Part of Lungs & breathing clinical trials.

This Phase 2 study tests whether HEC585 can slow the decline in lung function in people with progressive fibrosing interstitial lung disease (PF-ILD). It may help preserve breathing capacity and breathing tolerance over time.

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

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

Who can take part

  • Be at least 18 years old and be willing to sign the consent form and follow study visits.
  • You do NOT have idiopathic pulmonary fibrosis (IPF), but you do have progressive fibrosing interstitial lung disease confirmed on chest CT.
  • Despite at least 3 months of usual care, you must show recent worsening (symptoms, lung function test changes, and/or scan changes) within the past 12 months.
  • Your basic lung function tests must meet limits (FEV1/FVC at least 0.7 before bronchodilators, and %FVC at least 45% predicted).
  • Your DLCO (a gas-exchange test) must be between 30% and 80% of predicted.
  • If you have connective-tissue disease-related lung disease, your treatment must have been stable for 12 weeks before starting the study.

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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