Assessment of the Dose Reduction and Discontinuation Associated With Anti-Fibrotic Medications in Patients With Idiopathic Pulmonary Fibrosis

10/11/2026
10/11/2026
EU PAS number:
EUPAS1000001179
Study
Finalised
Study identification

EU PAS number

EUPAS1000001179

Study ID

1000001179

Official title and acronym

Assessment of the Dose Reduction and Discontinuation Associated With Anti-Fibrotic Medications in Patients With Idiopathic Pulmonary Fibrosis

DARWIN EU® study

No

Study countries

United States

Study description

The overarching aim of our study is to assess the incidence of dose reduction and discontinuations for pirfenidone and nintedanib.

Study status

Finalised
Research institutions and networks
No information provided.

Contact details

Boehringer Ingelheim

Primary lead investigator

Study timelines

Date when funding contract was signed

Actual:

Study start date

Actual:

Date of final study report

Planned:
Actual:
Sources of funding

More details on funding

No information provided.
Regulatory

Was the study required by a regulatory body?

Unknown

Is the study required by a Risk Management Plan (RMP)?

Not applicable