Clinical Progression of Mild to Moderate Idiopathic Pulmonary Fibrosis (IPF) Under a Therapy With Esbriet® (Pirfenidone)
NCT02622477 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 12
Last updated 2017-02-28
Summary
The purpose of the study was to assess the clinical outcome of patients with a mild to moderate IPF after a one-year therapy with Esbriet® (Pirfenidone).
Conditions
Interventions
- DRUG
-
This is an observational study. Pirfenidone is available as an 267 mg capsule for oral administration.
Sponsors & Collaborators
-
InterMune Deutschland GmbH
collaborator INDUSTRY - lead INDUSTRY
Principal Investigators
-
Clinical Trials · Hoffmann-La Roche
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2014-06-30
- Primary Completion
- 2016-12-31
- Completion
- 2016-12-31
Countries
- Germany
Study Locations
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