Immunomodulatory Treatment of Interstitial Lung Disease Associated With Surfactant Related Gene Variants
- Sponsor
- Assistance Publique - Hôpitaux de Paris
- Study ID
- NCT07443436
- Phase
- PHASE2
- Status
- Not Yet Recruiting
Notify me when recruiting opens
Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.
Add your contact details and location so we can keep your interest tied to this study.
Conditions
- Interstitial Lung Disease
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 80 Years
- Healthy Volunteers
- Not accepted
Interventions
- Azithromycin 250 mg x3/week (3 tablets/week) — DRUGRoute of administration: oral route Duration of treatment: 12 months Market authorization: yes Use in their market authorization indication: no
- Prednisone 10 mg/day — DRUGRoute of administration: oral route Duration of treatment: 12 months Market authorization: yes Use in their market authorization indication: no
- Hydroxychloroquine 400 mg/day — DRUGRoute of administration: oral route Duration of treatment: 12 months Market authorization: yes Use in their market authorization indication: no
- Active Comparator: Standard of care — DRUGStandard of care: any symptomatic treatment to interstitial lung disease. No other experimental or off-label treatment (such as ivacaftor) will be allowed during the study.
Study Details
Scientific justification : Variants in surfactant-related genes (SRG) explain approximately 6% of familial pulmonary fibrosis (FPF). The pathophysiology is unknown and seems to involve endoplasmic reticulum stress in type 2 alveolar epithelial cells. Variable improvement in the prognosis of childhood and adult interstitial lung disease (ILD) associated with a variant of a SRG, initially reported to be lethal within months of diagnosis, has been observed since the consensual use of prednisone, azithromycin and hydroxychloroquine targeting endoplasmic reticulum stress, without demonstration of the efficacy of any of these treatments alone or in combination. The investigators hypothesize that a treatment combining prednisone, azithromycin and hydroxychloroquine is safe and could improve the prognosis of adult patients with ILD associated with SRG variant. Main objective and primary endpoint : Main objective: Evaluate the efficacy of triple immunomodulatory therapy (prednisone, azithromycin and hydroxychloroquine) for 12 months in patients with ILD associated with a variant of a surfactant-related gene. Primary endpoint: Difference in forced vital capacity decline between the 2 groups at one year. Secondary objectives and endpoints : Secondary objectives: 1. tolerance of the triple therapy, 2. correlation between the respiratory, radiological and clinical functional response, 3. quality of life of the patients, 4. overall survival, transplant-free survival, exacerbation free-survival, hospitalization-free survival Secondary endpoints: 1. Clinical and biological tolerance (occurrence of an adverse effect during treatment), ECG (at 3, 6, 9, 12 months after randomization) (only HCQ or AZI patients) and ophthalmological (at one year after randomization) 2. Thoracic CT scan and PFT at 6 months and one year after randomization 3. Quality of life questionnaire (EORTC QLQ-C30, v3.0) at 3 months, 6 months, 9 months and one year after randomization, 4. Collection of vital status, lung transplantation, hospitalization for pulmonary and non-pulmonary causes and episodes of exacerbation at each visit until the end of follow-up 12 months after randomization. Design of the study : Multicenter, randomized, controlled, two-arm, parallel, open-label superiority study comparing triple immunomodulatory therapy (prednisone, azithromycin, and hydroxychloroquine) to standard of care Category : Category 2 Population of study participants: Patients aged over 18 years with ILD and SRG variant Number of participants included : 30 Design of the study : Multicenter, randomized, controlled, two-arm, parallel, open-label superiority study comparing triple immunomodulatory therapy (prednisone, azithromycin, and hydroxychloroquine) to standard of care.
Key Dates
- First listed
- Mar 2, 2026
- Start date
- Oct 1, 2026
- Status verified
- Jan 2026
- Primary completion
- Oct 1, 2027
- Completion
- Oct 1, 2027
Study Design
- Enrollment
- 30 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Prednisone 10 mg/day -Hydroxychloroquine 400 mg/day - Azithromycin 250mg*3The experimental treatment will be the combination of: * Prednisone 10 mg/day (1 tablet/day) * Hydroxychloroquine 400 mg/day (2 tablets/day) * Azithromycin 250 mg x3/week (3 tablets/week) Route of administration: oral route Duration of treatment: 12 months Market authorization: yes Use in their market authorization indication: no
- Active Comparator: Standard of careStandard of care: any symptomatic treatment to interstitial lung disease. No other experimental or off-label treatment (such as ivacaftor) will be allowed during the study.
Primary Outcome Measure
Difference in forced vital capacity decline between the 2 groups at one year. [ Time Frame: 12 Months ]
Central Contacts
- Annabelle METOIS0140257939annabelle/[email protected]
- BORIE Raphaël
Related Studies
- Hyperpolarized 129Xe MRI for Imaging Pulmonary FunctionPHASE2 · Recruiting · Bastiaan Driehuys · Durham, North Carolina
- WTC Chest CT Imaging ArchiveEnrolling By Invitation · Icahn School of Medicine at Mount Sinai · New York, New York
- Rheumatoid Arthritis Patients at Risk for Interstitial Lung DiseaseRecruiting · University of Colorado, Denver · Aurora, Colorado
- Creation of a Biospecimen Repository From Patients With Interstitial Lung Diseases (ILD)Recruiting · Mayo Clinic · Rochester, Minnesota