NCT00698568已完成3 期
Study to Evaluate the Safety of GSK Biologicals' Herpes Simplex Candidate Vaccine (gD2t) With MPL in HSV Seropositive or Seronegative Subjects Without Genital Herpes Disease
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 7,460
- 试验地点
- 47
- 主要终点
- To compare between herpes simplex vaccine and placebo recipients the general safety of the vaccine by recording all the unsolicited adverse experiences and all serious adverse experiences
研究概览
简要总结
This study will evaluate, versus a placebo, the safety of Herpes simplex candidate vaccine with adjuvant in initially HSV seropositive or seronegative subjects who have no genital herpes disease.
详细描述
This study was monitored by a Data Safety Monitoring Board. At the time of conduct of this study, the sponsor GlaxoSmithKline was known by its former name SmithKline Beecham.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •18 years of age and over at the time of first vaccination
- •Written informed consent
- •Females of childbearing potential must have a negative pregnancy test at enrollment and prior to each vaccination and be using an accepted method of birth control
排除标准
- •Any previous history of or current clinical signs or symptoms of genital herpes disease.
- •Any previous vaccination against herpes simplex.
- •Any previous administration of MPL.
- •History of herpetic keratitis.
- •History of erythema multiforme.
- •Female subjects who are pregnant, lactating or planning a pregnancy before one month after the last vaccine dose
- •Patient is immuno-compromised or is receiving immuno-modifying therapy of any kind. Topical corticoid therapy is allowed.
- •HIV positive at the time of enrollment
- •Clinical signs of acute or febrile illness at the time of entry into the study.
- •Any continuous suppressive antiviral oral therapy within the 6 months prior to entry.
- •Any administration of immunoglobulins during the vaccination course or within one month prior to the first vaccination.
- •Any vaccine administration less than one week before or after a study vaccination.
- •Previous known hypersensitivity to vaccination or to any component of the vaccine.
- •Simultaneous participation in any other clinical trial of an investigational drug or vaccine concurrent with this study or during the period beginning 30 days prior to entry into the study or 5 half-lives of the drug
- •Recent history of alcoholism or drug abuse
- •Recent clinical history or evidence of significant hepatic disease
- •History of a current acute or chronic auto immune disease.
- •Recent clinical history or evidence of renal dysfunction
- •Life-threatening or serious cardiac (NYHA grades III-IV), gastrointestinal, haematological or immunological disorder which, in the opinion of the investigator, would preclude entry into the study.
- •Inability or unwillingness to comply with the protocol or not expected to complete the study period
结局指标
主要结局
To compare between herpes simplex vaccine and placebo recipients the general safety of the vaccine by recording all the unsolicited adverse experiences and all serious adverse experiences
时间窗: During a 30-day period after each vaccination (AEs), during 7 months after study start (SAEs)
次要结局
- To compare between vaccine and placebo recipients the effect on pre-existing herpes simplex virus infection by recording the frequency and severity of all herpes simplex clinical episodes(Day 0 through month 19)
- To evaluate the incidence and the types of the serious adverse experiences in both groups(Month 7 to month 19)
- To compare between vaccine and placebo recipients the incidence and severity of the reactogenicity as measured by recording the local reactions and the general symptoms(On the day of each vaccination and on the following 3 days)
- To compare between vaccine and placebo recipients the effect on the haematological and biochemical parameters in subjects from 20% of the centers in each country(At day -90 to day -7, and at month 7 and month 13)
- To evaluate the humoral immune response to the vaccine by measuring the anti-gD2 antibodies in a subset of vaccine and placebo recipients from each of the serostatus groups(Before vaccination, and one month and 7 months after vaccination)
- To compare the anti-gD2 antibody responses between the subsets of HSV double seronegative and HSV-1 seropositive only vaccine recipients(At months 7 and 13)
研究者
研究点 (47)
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