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Real-life-persistence to Antifibrotic Treatments (REPEAT)

Boehringer Ingelheim logo

Boehringer Ingelheim

Status

Active, not recruiting

Conditions

Idiopathic Pulmonary Fibrosis

Treatments

Drug: Nintedanib
Drug: Pirfenidone

Study type

Observational

Funder types

Industry

Identifiers

NCT06485635
1199-0568

Details and patient eligibility

About

This study will help to better understand the persistence rate to antifibrotic (AF) treatment in real life in France and to identify potential areas for improvement by investigating the factors associated with a non-persistence rate to AF treatment.

Primary objective of the study is to measure the percentage of patients still treated up to 30 months after AF treatment initiation.

Enrollment

10,646 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

All patients with a reimbursement of AF treatment between 2018 and 2022 will be included for analysis.

Exclusion criteria

No exclusion criteria will be applied.

Trial design

10,646 participants in 1 patient group

Patients with a reimbursement of AF treatment
Treatment:
Drug: Pirfenidone
Drug: Nintedanib

Trial contacts and locations

1

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Central trial contact

Boehringer Ingelheim

Data sourced from clinicaltrials.gov

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