Efficacy and Safety of Early Antifibrotic Therapy for Non-progressive Fibrotic Interstitial Lung Disease

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age40-85
SponsorShanghai Pulmonary Hospital, Shanghai, China

About this trial

Early antifibrotic therapy for f-ILD

Eligibility criteria

Qualifiers

None

Disqualifiers

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);

Trial design

Treatments tested in this trial

  • Antifibrotic drugs (nidanib or pirfenidone)

Treatment groups

104 Participants
are divided into 2 treatment groups

Locations

This trial has no locations