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Real-life-persistence to Antifibrotic Treatments

Real-life-Persistence to Antifibrotic Treatments

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06485635
Acronym
REPEAT
Enrollment
10646
Registered
2024-07-03
Start date
2024-10-16
Completion date
2026-04-07
Last updated
2026-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Idiopathic Pulmonary Fibrosis

Brief summary

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.

Interventions

DRUGNintedanib

Nintedanib

DRUGPirfenidone

Pirfenidone

Sponsors

Boehringer Ingelheim
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

No

Design outcomes

Primary

MeasureTime frame
Persistence to antifibrotic (AF) treatment (measured as percentage of patients still treated up to 30 months after AF treatment initiation)up to 30 months

Secondary

MeasureTime frameDescription
AF prevalence in French populationup to 5 years
AF incidence in French populationup to 4 years
Number of AF treated patients split by indicationup to 2 yearsIndications: * Idiopathic Pulmonary Fibrosis (IPF) * Interstitial Lung Disease associated with Systemic Sclerosis (SSc-ILD) * Progressive Pulmonary Fibrosis (PPF)
Number of patients adherent to AF treatmentup to 30 monthsIn incident AF patients, percentage of days covered (PDC) will be calculated at different time point to measure the adherence to AF treatment for patients persistent to treatment at this time point. The PDC is the ratio dividing the number of days exposed by the number of days in the period evaluated. A PDC≥ 80% is considered as a good adherence to medication.
Percentage of the target cumulative dose of treatment received by the patientsup to 30 months
Influence of factors (yes/no) associated with persistence to AF treatmentsup to 30 monthsFor a pre-determined list of variables (as defined in the study protocol) in incident AF patients, a multivariate time-dependant Cox model will test several covariates to check if they are associated with persistence to AF treatment.
Number of patients with switch from one AF treatment to the another with no treatment stopup to 5 years
Number of patients at site of follow-up (identified as 2 lung function tests performed in the center)up to 5 years
Overall Survival (defined as time from index date (first reimbursement of AF treatment) to death from any cause)up to5 years
Event-free survivalup to 5 yearsDefined as the time from index date to * oxygenotherapy onset * hospitalisation for respiratory exacerbations * hospitalisation for other respiratory diseases * ath from any cause

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 16, 2026