Safety of Nintedanib in Real World in China

NCT05676112 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2024-12-10

No results posted yet for this study

Summary

The main objective of this study is to evaluate the incidence rates of adverse drug reactions (ADRs) and fatal adverse events (AEs) among idiopathic pulmonary fibrosis (IPF) patients in China who initiate nintedanib during the study period.

Conditions

Interventions

DRUG

nintedanib

nintedanib

DRUG

pirfenidone

pirfenidone

Sponsors & Collaborators

Eligibility

Min Age
40 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-12-29
Primary Completion
2026-09-30
Completion
2026-09-30

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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 NCT05676112 on ClinicalTrials.gov