RECRUITING

A Study to Test Whether Nerandomilast Helps People With Lungfibrosis Related to Rheumatic Diseases

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Adults 18 years of age and older or above legal age with lung fibrosis related to systemic autoimmune rheumatic disease can participate in this study. People can only take part if they show no improvement in lung function after standard treatment with immunosuppressant medicine. The main purpose of this study is to find out how a medicine called nerandomilast affects the lungs in people with systemic autoimmune rheumatic disease. Participants are put into 2 groups randomly, which means by chance. One group takes nerandomilast tablets and the other group takes placebo tablets. Placebo tablets look like nerandomilast tablets but do not contain any medicine. Participants take a tablet 2 times a day for at least 26 weeks and up to 1 year. Participants continue immunosuppressant treatment for their underlying rheumatic disease. Participants are in the study for about 7.5 to 13 months depending on when they join the study. During this time, they visit the study site about 9 to 10 times. At study visits, participants have lung function tests. At select visits, chest imaging is performed. Participants fill in questionnaires about their symptoms and quality of life. The results between the 2 groups are compared to see whether the treatment works. The doctors also regularly check participants' health and take note of any unwanted effects.

Official Title

A Double Blind, Randomised, Placebo-controlled Trial Evaluating the Efficacy and Safety of Nerandomilast Over at Least 26 Weeks in Patients With Systemic Autoimmune Rheumatic Diseases Associated Interstitial Lung Diseases (SARD-ILD)

Quick Facts

Study Start:2025-09-13
Study Completion:2027-07-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06806592

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Boehringer Ingelheim
CONTACT
1-800-243-0127
clintriage.rdg@boehringer-ingelheim.com

Study Locations (Sites)

University of Alabama at Birmingham
Birmingham, Alabama, 35294
United States
Mayo Clinic-Arizona
Scottsdale, Arizona, 85259
United States
University of California Los Angeles
Los Angeles, California, 90095
United States
Paradigm Clinical Research - San Diego
San Diego, California, 92108
United States
National Jewish Health
Denver, Colorado, 80206
United States
Yale University School of Medicine
New Haven, Connecticut, 06510
United States
Meris Clinical Research-Brandon-69466
Brandon, Florida, 33511
United States
Miami VA Healthcare System
Miami, Florida, 33125
United States
Piedmont Hospital
Atlanta, Georgia, 30309
United States
Augusta University
Augusta, Georgia, 30912
United States
Northwestern University
Chicago, Illinois, 60611
United States
University of Chicago
Chicago, Illinois, 60637
United States
Evanston Hospital
Evanston, Illinois, 60201
United States
University of Kansas Medical Center
Kansas City, Kansas, 66160
United States
LSU Health Sciences Center
New Orleans, Louisiana, 70112
United States
Massachusetts General Hospital
Boston, Massachusetts, 02114
United States
Brigham and Women's Hospital
Boston, Massachusetts, 02115
United States
University of Minnesota
Minneapolis, Minnesota, 55455
United States
Mayo Clinic
Rochester, Minnesota, 55905
United States
University of Nebraska Medical Center
Omaha, Nebraska, 68198-1230
United States
Northwell Health
Great Neck, New York, 11021
United States
NYU Langone Health
New York, New York, 10017
United States
Columbia University Medical Center-New York Presbyterian Hospital
New York, New York, 10024
United States
Onsite Clinical Solutions
Salisbury, North Carolina, 28144
United States
Southeastern Research Center-Winston Salem-69289
Winston-Salem, North Carolina, 27103
United States
Cleveland Clinic
Cleveland, Ohio, 44195
United States
Temple Lung Center
Philadelphia, Pennsylvania, 19140
United States
University of Pittsburgh Medical Center
Pittsburgh, Pennsylvania, 15213
United States
The University of Texas Health Science Center at Houston
Houston, Texas, 77030
United States
University of Texas Health Science Center at San Antonio
San Antonio, Texas, 78229
United States
University of Utah Health Sciences Center
Salt Lake City, Utah, 84108
United States
Rheumatology and Pulmonary Clinic
Beckley, West Virginia, 25801
United States
University of Wisconsin
Madison, Wisconsin, 53792
United States

Collaborators and Investigators

Sponsor: Boehringer Ingelheim

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-09-13
Study Completion Date2027-07-30

Study Record Updates

Study Start Date2025-09-13
Study Completion Date2027-07-30

Terms related to this study

Additional Relevant MeSH Terms

  • Interstitial Lung Diseases
  • Systemic Autoimmune Rheumatic Diseases Associated Interstitial Lung Diseases