Varicella Clinical Trial
Official title:
Re-examination Study for General Vaccine Use to Assess the Safety Profile of Varivax in Usual Practice
This survey is conducted for preparing application materials for re-examination under the Korean Pharmaceutical Affairs Laws and its Enforcement Regulation; its aim is to reconfirm the clinical usefulness of VARIVAX through collecting the safety information according to the Re-examination Regulation for New Drugs.
This post-marketing survey was conducted in the usual routine practice and the investigator enrolled participants vaccinated with VARIVAX continuously after study start. The purpose of the study was to assess the occurrence of adverse events and to identify factors that may affect the safety of the vaccine under real-life, post-marketing conditions. No hypothesis testing was conducted in this survey. ;
Time Perspective: Prospective
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|---|---|---|---|
| Completed |
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Phase 3 | |
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Phase 3 | |
| Completed |
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Phase 1/Phase 2 | |
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Phase 3 | |
| Completed |
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Phase 3 | |
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| Completed |
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Phase 3 |