Special Drug Use Investigation for Relenza® (Zanamivir) (Prophylaxis)
NCT01390792 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 622
Last updated 2017-05-16
Summary
The purpose of this post-marketing surveillance study is to collect information on efficacy and safety for prophylactic administration of zanamivir in clinical practice in family or persons living with patients with influenza virus infection.
Conditions
- Influenza, Human
Interventions
- DRUG
-
Zanamivir hydrate
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
GSK Clinical Trials · GlaxoSmithKline
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2007-01-31
- Primary Completion
- 2009-02-28
- Completion
- 2009-05-31
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