PRospective phenotypIng and Multi-omic Endotyping of Progressive Pulmonary Fibrosis

NCT06855329 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2025-09-22

No results posted yet for this study

Summary

This is a prospective, observational cohort study. Participants with non-idiopatic pulmonary fibrosis, interstitial lung disease (ILD) will be followed for 24 months to systematically collect clinical, imaging, and biospecimen data. The primary objective is to optimize progressive pulmonary fibrosis (PPF) classification and establish PPF incidence for key ILD subtypes. Additional exploratory objectives are to 1) Prospectively validate a novel PPF classifier and assess performance durability over time, and 2) Determine whether multi-dimensional PPF prediction outperforms component approaches.

Conditions

Sponsors & Collaborators

  • University of Michigan

    collaborator OTHER
  • University of Virginia

    collaborator OTHER
  • Johannes Gutenberg University Mainz

    collaborator OTHER
  • Fondazione Policlinico Universitario Agostino Gemelli IRCCS

    collaborator OTHER
  • University of Massachusetts, Worcester

    lead OTHER

Principal Investigators

  • Fernando J Martinez, MD, MS · University of Massachusetts Chan Medical School

  • Justin Oldham, MD, MS · University of Michigan

  • Cathie Spino, DSc · University of Michigan

  • Imre Noth, MD, MS · University of Virginia

  • Michael Kreuter, MD · Johannes Gutenberg University Mainz

  • Dinesh Khanna, MD, MS · University of Michigan

  • Luca Richeldi, MD, PhD · Policlinico Gemelli

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-05-01
Primary Completion
2029-12-31
Completion
2029-12-31

Countries

  • United States
  • Australia
  • Canada
  • Ireland
  • United Kingdom

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06855329 on ClinicalTrials.gov