Dose Reduction and Discontinuation With Anti-Fibrotic Medications

NCT05779007 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 2778

Last updated 2025-07-28

Study results available
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Summary

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

Conditions

Interventions

DRUG

Pirfenidone

Pirfenidone

DRUG

Nintedanib

Nintedanib

Sponsors & Collaborators

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-04-18
Primary Completion
2023-07-14
Completion
2023-07-14
FDA Drug
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05779007 on ClinicalTrials.gov