Post Marketing Surveillance of Roflumilast in Korea

NCT02068456 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1837

Last updated 2017-06-22

No results posted yet for this study

Summary

The purpose of this study is to evaluate the safety and efficacy of roflumilast in the real-use conditions with its registered indications.

Conditions

Interventions

Sponsors & Collaborators

Principal Investigators

  • AstraZeneca AstraZeneca · AstraZeneca

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-09-18
Primary Completion
2017-04-26
Completion
2017-04-26

Countries

  • South Korea

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 NCT02068456 on ClinicalTrials.gov