IPF, PPF, and non-progressive ILD
Conditions
Interventions
None listed
Sponsors
Nippon Boehringer Ingelheim Co., Ltd
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients diagnosed with at least 2 fibrosing ILD codes in different months during the patient identification period Patients aged 20 years or older on the index date Patients for whom data for the 12 months prior to the index date can be extracted as baseline data
Exclusion criteria
Exclusion criteria: None
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To describe patient journey in patients with fibrosing Interstitial Lung Diseases (ILDs) in Japan. | — |
Secondary
| Measure | Time frame |
|---|---|
| To describe baseline demographic and clinical characteristics in patients with fibrosing ILDs in Japan. To investigate the initial symptoms prior to the diagnosis of fibrosing ILDs in patients with fibrosing ILDs in Japan. To investigate the time from the development of Progressive Pulmonary Fibrosis (PPF) to initiation of the PPF treatment in patients with PPF in Japan. To investigate the proportions of patients having each of the Idiopathic Pulmonary Fibrosis (IPF) and PPF treatments in patients with IPF and PPF in Japan. To investigate the time from PPF treatment to death in patients with PPF in Japan. To investigate the proportions of patients meeting each PPF criterion among those meeting any of the 9 PPF criteria in Japan. | — |
Countries
Japan
Contacts
Public ContactTsuyoshi Ishii
Nippon Boehringer Ingelheim Co., Ltd. Medicine Division
Outcome results
None listed