Regulatory Nebilet PMS
NCT01077661 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 743
Last updated 2017-05-30
Summary
An open label, multi-centre, non-interventional post-marketing surveillance (PMS) to monitor the safety and effectiveness of Nebivolol administered in Korean patients according to the prescribing information
Conditions
Interventions
- DRUG
-
Nebivolol
patients administrated Nebivolol according to the prescribing information
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
GSK Clinical Trials · GlaxoSmithKline
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2009-10-31
- Primary Completion
- 2010-12-31
- Completion
- 2011-01-31
Countries
- South Korea
Study Locations
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