TIPS : Immunomodulatory Treatment of Interstitial Lung Disease Associated with Surfactant related Gene Mutations
Condition studied
Interstitial Lung Disease
Investigational medicinal product(s)
Every trial of Azithromycin, Hydroxychloroquine, Prednisolone and Prednisone across our registers →
Eligibility
Primary endpoint
Difference in forced vital capacity decline between the 2 groups at one year
Endpoint detail
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), Thoracic CT scan and PFT at 6 months and one year after randomization, Quality of life questionnaire (EORTC QLQ-C30, v3.0) at 3 months, 6 months, 9 months and one year after randomization,, 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
This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View 2026-525336-41-00 on CTIS ↗ ← All trials in the EU