Clin2
NCT06325696Possibly a fitRecruiting

H01 for adults with lung scarring (SOLIS study)

Interstitial Lung DiseaseIdiopathic Pulmonary FibrosisLung Diseases, Interstitial

Part of Lungs & breathing clinical trials.

This study tests an oral medication (H01/hymecromone) to see if it can help people with progressive lung scarring (ILD). It lasts about 12 to 24 weeks and requires good lung function without needing oxygen at rest.

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

Phase
Phase 2
Enrollment
37 people
Ages
18 years to 100 years
Study type
Interventional

Who can take part

  • You must be at least 18 years old.
  • You have a diagnosis of Idiopathic Pulmonary Fibrosis or another progressive lung scarring disease.
  • Your lung function tests (DLCO and FVC) must be above certain minimum levels (DLCO >30% and FVC >45% of normal).
  • If you can become pregnant or father a child, you must agree to use effective contraception during the study.
  • You cannot be on the lung transplant list, need oxygen at rest, or have certain other medical conditions like liver disease or celiac disease.

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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