Ireland
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Clinical Trials in the EU / 2026-525336-41-00
Authorised, not yet recruiting Phase II

TIPS : Immunomodulatory Treatment of Interstitial Lung Disease Associated with Surfactant related Gene Mutations

2026-525336-41-00 · tracked via the Priya Life Science EU tracker
Sponsor type
Hospital/Clinic/Other health care facility
Therapeutic area
Respiratory Tract Diseases
Decision date
14/08/2026
Enrollment target
30
Sites
France

Condition studied

Interstitial Lung Disease

Investigational medicinal product(s)

PREDNISOLONEPREDNISONEAZITHROMYCINHYDROXYCHLOROQUINE

Every trial of Azithromycin, Hydroxychloroquine, Prednisolone and Prednisone across our registers →

Eligibility

Age group
65+ years, 18-64 years
Sex
Female, Male

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

Official registry record

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