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Clinical Trials in China / NCT07497087
Recruiting Phase 3

A Study to Test Whether Nerandomilast Helps People With Systemic Sclerosis

NCT07497087 · tracked via the Priya Life Science China tracker
Sponsor
Boehringer Ingelheim
Phase
Phase 3
Started
2026-07-27
Last updated
2026-09-17

Condition(s) studied

Systemic Sclerosis

Investigational drug(s) / intervention(s)

Placebo matching nerandomilast formulation 1Placebo matching nerandomilast formulation 2Nerandomilast formulation 1Nerandomilast formulation 2

Placebo matching nerandomilast formulation 1: Film-coated tablets

Placebo matching nerandomilast formulation 2: Film-coated tablets

Nerandomilast formulation 1: Film-coated tablets

Nerandomilast formulation 2: Film-coated tablets

Study summary

Nerandomilast is being developed to help people with systemic sclerosis by potentially improving symptoms and slowing disease progression. This study is open to adults who are at least 18 years old and have systemic sclerosis (SSc). People can join the study if they have limited or diffuse cutaneous SSc with disease onset within 7 years of the first non-Raynaud's symptom. The purpose of this study is to find out whether a medicine called nerandomilast helps people with systemic sclerosis. This study also aims to find out how well nerandomilast is tolerated in people with systemic sclerosis.

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 the tablets twice a day.

Participants are in the study for 1 to about 4 years. During this time, they visit the study site regularly and get phone calls from the site staff. During study visits participants regularly have blood samples taken and doctors check changes in skin thickening, lung function, and internal organs, overall health and the safety and tolerability of study treatment in people with SSc. The results are compared between the groups to see whether the treatment works. The doctors also regularly check participants' health and take note of any unwanted effects.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion criteria: 1. Signed and dated written informed consent in accordance with ICH-GCP and local legislation prior to admission to the trial. 2. Patients must be at least 18 years of age and fulfil the 2013 American College of Rheumatology/European Alliance of Associations for Rheumatology (ACR/EULAR) criteria for SSc. 3. Patients must be diagnosed with limited cutaneous SSc (lcSSc) or diffuse cutaneous SSc (dcSSc), as defined by LeRoy et al. (1988). 4. Disease onset (defined by first non-RP \[Raynaud's phenomenon\] symptom) must be within 7 years of Visit 1. 5. Trial participants with dcSSc must have evidence of active disease during screening. 6. Trial participants with lcSSc must have evidence of active disease during screening. LcSSc patients must be anti-centromere antibody (ACA) negative. 7. FVC % predicted ≥45% at Visit 1. 8. Diffusing Capacity of the Lungs for Carbon Monoxide (DLCO) % predicted ≥25% corrected for haemoglobin (Hb) at Visit 1. 9. Women of childbearing potential (WOCBP) must be ready and able to use highly effective methods of birth control. 10. Patients may be either untreated or on stable treatment with permitted immunosuppressive/immunomodulatory agents and/or nintedanib. All treatments must remain stable prior to Visit 2 and during the screening period Exclusion criteria: 1. Active, unstable, or uncontrolled vasculitis within 8 weeks prior to Visit 1 or during the screening period. 2. Any suicidal behaviour in the past 2 years. 3. Any suicidal ideation of type 4 or 5 on the C-SSRS in the past 3 months. Further exclusion criteria apply.

Primary outcome measure(s)

Trial sites (248)

FacilityCityRegionStatus
University of Alabama at Birmingham Birmingham Alabama Not Yet Recruiting
Banner - University Medicine Rheumatology Clinic Phoenix Arizona Not Yet Recruiting
Arizona Arthritis and Rheumatology Associates - Paradise Valley Scottsdale Arizona Not Yet Recruiting
University of California Los Angeles Los Angeles California Not Yet Recruiting
Paradigm Clinical Research - San Diego San Diego California Recruiting
Stanford University School of Medicine Stanford California Not Yet Recruiting
Medvin Clinical Research-Whittier-69033 Whittier California Recruiting
University of Colorado Denver Aurora Colorado Not Yet Recruiting
Georgetown University Washington D.C. District of Columbia Not Yet Recruiting
Millennium Research - Ormond Beach Ormond Beach Florida Recruiting
Integral Rheumatology and Immunology Specialist Plantation Florida Not Yet Recruiting
BioResearch Partner - South Miami South Miami Florida Recruiting
Northwestern University Chicago Illinois Not Yet Recruiting
The University of Chicago Medical Center Chicago Illinois Not Yet Recruiting
DelRicht Research-New Orleans-64100 New Orleans Louisiana Recruiting
Johns Hopkins Hospital Baltimore Maryland Not Yet Recruiting
Massachusetts General Hospital Boston Massachusetts Not Yet Recruiting
University of Michigan Ann Arbor Michigan Not Yet Recruiting
Clinical Research Institute of Michigan, LLC - St. Clair Shores Saint Clair Shores Michigan Not Yet Recruiting
M Health Fairview University of Minnesota Medical Center Minneapolis Minnesota Not Yet Recruiting
Rutgers Robert Wood Johnson Medical School New Brunswick New Jersey Not Yet Recruiting
Hospital for Special Surgery New York New York Not Yet Recruiting
Icahn School of Medicine at Mount Sinai New York New York Not Yet Recruiting
Columbia University Medical Center-New York Presbyterian Hospital New York New York Not Yet Recruiting
University of Pennsylvania Philadelphia Pennsylvania Not Yet Recruiting
Thomas Jefferson University Philadelphia Pennsylvania Recruiting
West Tennessee Research Institute Jackson Tennessee Recruiting
Tekton Research, Inc - West Gate Boulevard Austin Texas Recruiting
Arthritis & Rheumatology Institute - Frisco Frisco Texas Recruiting
The University of Texas Health Science Center at Houston Houston Texas Not Yet Recruiting
Centro Medico Reumatologico - OMI CABA Argentina Recruiting
Mautalen- Salud e Investigacion CABA Argentina Recruiting
Instituto de Investigacion Clinica TyT CABA Argentina Recruiting
Sanatorio Maipu Maipu Argentina Recruiting
Instituto de Investigaciones Clinicas de Quilmes Quilmes Argentina Recruiting
Sanatorio de la Mujer Rosario Argentina Recruiting
Westmead Hospital Westmead New South Wales Not Yet Recruiting
Royal Adelaide Hospital Adelaide South Australia Not Yet Recruiting
St Vincent's Hospital Melbourne Fitzroy Victoria Not Yet Recruiting
Medizinische Universitaet Innsbruck Innsbruck Austria Not Yet Recruiting

+ 208 more sites — see the full list on the official registry below.

More Boehringer Ingelheim trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07497087 on ClinicalTrials.gov ↗ ← All trials in China