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NCT06714812: EAD-IPF-N

Diarrheal Adverse Events in Caucasian Patients With Idiopathic Pulmonary Fibrosis Undergoing Treatment With Nintedanib

Active, enrolled Last updated 19 December 2025
What this trial tests

trial in IPF in 100 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
20 August 2023
Primary endpoint
31 December 2023
31 December 2025

Quick facts

Lead sponsorIRCCS Azienda Ospedaliero-Universitaria di Bologna
StatusActive, enrolled
Study typeOBSERVATIONAL
Enrollment100
Start date20 August 2023
Primary completion31 December 2023
Estimated completion31 December 2025
Sites1 location across Italy

Conditions studied

Sponsor

IRCCS Azienda Ospedaliero-Universitaria di Bologna — full company profile →

Who can join

18 and older, any sex, with IPF. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this observational study is to identify the demographic and clinical characteristics associated with the development of diarrheal adverse events in a Caucasian population with IPF undergoing treatment with nintedanib. Additionally this study aims to evaluate the different therapeutic strategies for dose reduction of nintedanib and assess the effectiveness of these strategies in reducing the occurrence of diarrhea.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for IPF

Currently open trials in the same condition.

Other IRCCS Azienda Ospedaliero-Universitaria di Bologna trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06714812.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing