Tests belimumab for lung scarring in people with scleroderma
Tests belimumab against a placebo in adults with scleroderma-related lung disease.
Key facts
- Who runs it
- GlaxoSmithKline
- Where
- Bobigny, Brest, Paris, Paris Cedex 13, and Toulouse Cedex 9, FranceSee the 5 sitesAlso in 17 other countries, 112 sites
- Trial code
- Registry title
- A Study of the Efficacy and Safety of Belimumab in Adults With Systemic Sclerosis Associated Interstitial Lung Disease
- Status
- Recruiting
- Phase
- Phase 2/3
- People taking part
- 300 people, planned
- Started
- 13 Sept 2023
- Expected to end
- 25 Oct 2029
- Type of study
- Interventional, 2 groupsOne group gets a placebo (a dummy treatment), for comparison.
- Treatments tested
- Belimumab
- Placebo
- Record updated
- 8 September 2026
Who can take part
AI summary
From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.
The trial is looking for adults with diffuse systemic sclerosis and lung scarring (interstitial lung disease) who have active or worsening disease. It tests belimumab against placebo.
- Age
- 18 years or older
- Sex
- All sexes can join. Women who are pregnant or breastfeeding cannot join.
- Disease stage
- Systemic sclerosis with widespread skin thickening (total mRSS 15 or more) and interstitial lung disease seen on a chest CT scan. The disease is active or getting worse.
- Earlier treatment
- Some earlier treatments must have been stopped for a set time before the start: biologic drugs 3 months, rituximab 6 months, cyclophosphamide 6 months, anti-fibrotic drugs 4 weeks, IM or IV corticosteroids 1 month.
- Biomarker or test result
- Anticentromere antibody test must be negative.
Main reasons for not taking part
- Pulmonary arterial hypertension
- Very low lung function (FVC 45% of predicted or lower, or DLco 40% or lower) or needing extra oxygen
- Scleroderma-like illnesses or another main autoimmune rheumatic disease
- Systemic sclerosis kidney crisis in the past 6 months
- Past or planned organ or bone marrow transplant
The registry criteria, word for word
Show all 27 criteriaShow less
Who can take part
- Participant is 18 years of age inclusive, or older at the time of signing the informed consent
- Documented diagnosis of SSc as defined by the American College of Rheumatology / European League Against Rheumatism 2013 SSc classification criteria
- Diffuse cutaneous disease, defined as presence of thickened skin with mRSS >0 over at least one skin area proximal to elbows and/or knees in addition to distal areas involvement on Day 1
- Total mRSS ≥15 on Day 1
- Evidence of interstitial lung disease on centrally read screening HRCT
- Anticentromere antibody negative on central test at screening
- Evidence for active or progressive disease
- Participant has an area of uninvolved or mildly thickened skin that, in the opinion of the investigator, would allow SC injection at the abdomen or the front, middle region of the thigh
- Participant is capable and willing to self-administer the study medication or has a caregiver who is capable and willing to administer the study medication throughout the study
- A female participant is eligible to participate if she is not pregnant or breastfeeding, and one of the following conditions applies:; Is a Woman of Non-Childbearing Potential (WONCBP) OR Is a Woman of Childbearing Potential (WOCBP) and using a contraceptive method that is highly effective
- Capable of giving signed informed consent
Who cannot take part
- Pulmonary arterial hypertension, as determined by the investigator at, or prior to first day of dosing (Day 1)
- SSc renal crisis within 6 months prior to the first day of dosing (Day 1)
- Previous or planned major organ transplant (e.g., heart, lung, kidney, liver) or bone marrow transplant (e.g., autologous stem cell transplant)
- Treatment with biologic agents, such as intravenous immunoglobulin or monoclonal antibodies, including marketed drugs, within 3 months or 5 half-lives (whichever is longer) prior to dosing
- Treatment with rituximab within 6 months prior to Day 1
- Treatment with non-biologic systemic immunosuppressive medication, other than mycophenolate, methotrexate or azathioprine (including, but not limited to cyclosporine A, tacrolimus, leflunomide, oral or parenteral gold, Janus kinase (JAK) inhibitors) within 3 months prior to Day 1
- Treatment with cyclophosphamide (oral or intravenous) within 6 months prior to Day 1
- Use of anti-fibrotic agents including colchicine, D-penicillamine, pirfenidone or tyrosine kinase inhibitors (e.g., nintedanib, nilotinib, imatinib, dasatinib) within 4 weeks prior to Day 1
- Cytotoxic drugs such as, chlorambucil, nitrogen mustard, or other alkylating agents within 6 months of Day 1
- Treatment with IM or IV corticosteroids within 1 month prior to Day 1
- Systemic sclerosis-like illness, including but not limited to localized scleroderma (morphoea), eosinophilic fasciitis, sclerodermoid graft-versus-host disease, fibro mucinous conditions (scleroedema, scleromyxoedema), scleroderma-like conditions that are associated with environmental chemical and drug exposure (e.g., toxic rapeseed oil, vinyl chloride, bleomycin, gadolinium-based contrast agents [nephrogenic systemic fibrosis], or due to metabolic disease)
- Primary diagnosis of a rheumatic autoimmune disease other than dcSSc, including but not limited to rheumatoid arthritis, systemic lupus erythematosus, polymyositis, dermatomyositis, systemic vasculitis, Sjogren's syndrome, antisynthetase syndrome, or mixed connective tissue disease, as determined by the investigator
- History or presence of cardiovascular, respiratory, hepatic, renal, gastrointestinal, endocrine, hematologic, or neurological disorders capable of significantly altering the absorption, metabolism, or elimination of drugs; constituting a risk when taking the study intervention or interfering with the interpretation of data
- Obstructive pulmonary disease (pre-bronchodilator FEV1/FVC <0.7)
- FVC ≤45% of predicted, or a DLco (corrected for hemoglobin) ≤40% of predicted or requiring supplemental oxygen at screening
- Significant emphysema on screening HRCT (extent of emphysema exceeds extent of ILD)
Where in France
Also in 17 other countries, 112 sites
- Assistance Publique Hopitaux De ParisBobigny, FranceTaking people
- Centre Hospitalier Régional et Universitaire de BrestBrest, FranceTaking people
- Assistance Publique Hopitaux de ParisParis, FranceTaking people
- Assistance Publique Hopitaux De ParisParis Cedex 13, FranceTaking people
- Centre Hospitalier Universitaire De ToulouseToulouse Cedex 9, FranceTaking people
About the trial
What the trial wants to find out
This study investigates the efficacy and safety of belimumab compared to placebo, in addition to standard therapy, for the treatment of participants with systemic sclerosis associated interstitial lung disease (SSc-ILD). The study will evaluate the effect of belimumab treatment on lung function as well as on extra-pulmonary disease manifestations, including skin thickening and general symptoms, such as fatigue, that impact quality of life (QoL).
The 2 groups in the trial
- BelimumabTreatment being tested
Participants will receive belimumab in addition to standard therapy.
- PlaceboPlacebo, for comparison
Participants will receive placebo in addition to standard therapy.
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorData and sources
- Registry record
- Listed on ClinicalTrials.gov and on the EU's official list of trials (CTIS).
- Official title
- A Phase 2/3, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate The Efficacy And Safety of Belimumab Administered Subcutaneously in Adults With Systemic Sclerosis Associated Interstitial Lung Disease (SSC-ILD)
- Plain-language title
- Tests belimumab for lung scarring in people with sclerodermaGenerated from the registry record. The registry title is the official one.
- AI summary
- From the trial's eligibility criteria. Read by machine on 12 November 2026.
- Publications
- Systemic sclerosis: pathogenic mechanisms and their implications for treatment.Seminars in immunopathology, 2025
- Record updated
- 8 September 2026