Efficacy and Safety of Early Antifibrotic Therapy for Non-progressive Fibrotic Interstitial Lung … (NCT07141810) | Clinical Trial Compass
Not Yet RecruitingPhase 4
Efficacy and Safety of Early Antifibrotic Therapy for Non-progressive Fibrotic Interstitial Lung Disease
104 participantsStarted 2025-10-01
Plain-language summary
Early antifibrotic therapy for f-ILD
Who can participate
Age range40 Years – 85 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Exclusion criteria
✕. Patients with unstable disease (IPF) assessed by investigators during screening had acute exacerbations during screening or within 3 months before randomization;
✕. Patients who are likely to require lung transplantation within 6 months or whose expected survival is less than 1 year as assessed by the investigators at the time of screening;
✕. During screening, chest HRCT indicated that the range of emphysema exceeded the range of pulmonary fibrosis (based on independent imaging evaluation results);
✕. Patients with airway obstruction disease (such as FEV1/FVC after bronchodilator);
✕. Diagnosed with IPF
✕. Diagnosis of PPF according to the 2022 ATS/ERS/JRS/ALAT guidelines
✕. Patients with other types of respiratory diseases that the investigators assessed might affect the study results;
✕. Patients who need to receive oxygen therapy for 15 hours or more per day;
What they're measuring
1
FVC %predict
Timeframe: 48 weeks
Trial details
NCT IDNCT07141810
SponsorShanghai Pulmonary Hospital, Shanghai, China