πŸ›οΈ Verified NIH Record β€’ Updated 2026-08-19

A Follow-up Study to Test Long-term Treatment With Nerandomilast in People With Pulmonary Fibrosis Who Took Part in a Previous Study With Nerandomilast (NCT06238622)

An Open-label Extension Trial of the Long-term Safety and Efficacy of BI 1015550 Taken Orally in Patients With Idiopathic Pulmonary Fibrosis (IPF) and Progressive Pulmonary Fibrosis (PPF) (FIBRONEERβ„’-ON)

🟒 Recruiting Phase3 πŸ’Š Investigational Drug / Biologic Sponsor: Boehringer Ingelheim

🩺 Plain-English Summary (8th-Grade Level)

This study is open to people with idiopathic pulmonary fibrosis (IPF) or progressive pulmonary fibrosis (PPF). They can only take part if they have completed treatment in a previous study with a medicine called nerandomilast or BI 1015550. The goal of this study is to find out how well people with pulmonary fibrosis tolerate long- term treatment with nerandomilast. The study also tests whether nerandomilast improves lung function and prolongs the time until symptoms get worse, participants need to go to the hospital, or die. Every participant takes nerandomilast as tablets for up to 1 year and 10 months. The participants may also continue their regular treatment for pulmonary fibrosis during the study. Participants visit their doctors regularly. During these visits, the doctors collect information on any health problems of the participants. Participants also regularly do lung function tests.

Who can join: Review the eligibility criteria below.

Location: University of Alabama at Birmingham β€” Birmingham, Alabama

Age range: 18 Years

πŸ§ͺ Interventions in This Study

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ All Participating Trial Locations (373 Sites)

Showing the first 25 of 373 sites.

  • University of Alabama at Birmingham β€” Birmingham, Alabama
  • University of Arizona β€” Tucson, Arizona
  • University of Southern California β€” Los Angeles, California
  • Cedars-Sinai Medical Center β€” Los Angeles, California
  • University of California Los Angeles β€” Los Angeles, California
  • University of California Davis β€” Sacramento, California
  • National Jewish Health β€” Denver, Colorado
  • Yale University School of Medicine β€” New Haven, Connecticut
  • Christiana Hospital β€” Newark, Delaware
  • Georgetown University β€” Washington D.C., District of Columbia
  • St. Francis Medical Institute β€” Clearwater, Florida
  • University of Florida β€” Gainesville, Florida
  • Clinical Research Specialists LLC - Kissimmee β€” Kissimmee, Florida
  • Advanced Pulmonary Research Institute β€” Loxahatchee Groves, Florida
  • Piedmont Physicians Pulmonary & Sleep Medicine of Buckhead β€” Atlanta, Georgia
  • The Emory Clinic β€” Atlanta, Georgia
  • Northshore University Health System β€” Evanston, Illinois
  • University of Kansas Medical Center β€” Kansas City, Kansas
  • Tulane Medical Center β€” New Orleans, Louisiana
  • Johns Hopkins Hospital β€” Baltimore, Maryland
  • Massachusetts General Hospital β€” Boston, Massachusetts
  • Brigham and Women's Hospital β€” Boston, Massachusetts
  • St. Elizabeth's Medical Center β€” Boston, Massachusetts
  • Beth Israel Deaconess Medical Center β€” Boston, Massachusetts
  • University of Michigan β€” Ann Arbor, Michigan

πŸ“ž Contact the Study Coordinator

Phone: (800) 243-0127

Email: clintriage.rdg@boehringer-ingelheim.com

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

πŸ’° Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA Β§ 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

πŸ’‘ How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
πŸ›οΈ View Official NIH Record β†—