A Phase III Clinical Trial to Evaluate the Efficacy, Immunogenicity, Safety and Tolerability of ZOSTAVAX™ in Subjects 50 to 59 Years of Age - ZOSTAVAX™ in Subjects 50 to 59 Years of Age

Merck & Co., Inc.0 个研究点目标入组 20,300 人开始时间: 2007年9月28日最近更新: 2012年3月19日

适应症

试验速览

暂无简介。

•1. Age 50 to 59 years (at time of informed consent).
•2. Signed an informed consent form prior to any study procedure.
•3. Afebrile (<100.4°F [<38.0°C] oral or equivalent) on day of vaccination.
•4. History of varicella or residence in a VZV-endemic area for =30 years.
•5. Female subjects who are of reproductive potential must have a negative serum or urine pregnancy test and agree to remain abstinent, or use (or have their partner use) 2 acceptable methods of birth control for 3 months postvaccination.
•Are the trial subjects under 18? no
•Number of subjects for this age range:
•F.1.2 Adults (18-64 years) yes
•F.1.2.1 Number of subjects for this age range
•F.1.3 Elderly (>=65 years) no
•F.1.3.1 Number of subjects for this age range

•1. A history of hypersensitivity reaction to any vaccine component, including gelatin or neomycin.
•2. Prior receipt of any varicella or zoster vaccine.
•3. Prior history of HZ.
•4. Immunoglobulin or any blood products given 5 months prior to vaccination or expected during the 42 days after vaccination.
•5. Any live virus vaccine administered within 4 weeks prevaccination or expected within 42 days postvaccination.
•6. Any inactivated vaccine administered within 7 days prevaccination or expected within 7 days postvaccination.
•7. Subject is pregnant or breastfeeding.
•8. Participation in a clinical study with administration of an investigational drug or vaccine within the last 30 days prior to enrollment.
•9. An intercurrent illness that might interfere with the interpretation of the study.
•10. Use of immunosuppressive therapy.
•11. Known or suspected immune dysfunction.
•12. Any concomitant use of nontopical antiviral therapy.

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