EUCTR2007-002771-14-DE进行中（未招募）不适用
COMPARISON OF THREE COMMERCIAL BATCHES OF THE JAPANESE ENCEPHALITIS VACCINE IC51. DOUBLE BLIND, RANDOMIZED, CONTROLLED PHASE 3 STUDY
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- Intercell AG
- 入组人数
- 384
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •- At least 18 years of age
- •- In female subjects, either childbearing potential terminated by surgery or 1 year post menopausal, or a negative serum pregnancy test during screening and the willingness not to become pregnant during the entire study period by practicing reliable methods of contraception, as specified in protocol Section 6.4
- •- Written informed consent obtained prior to study entry (subjects should give their consent themselves)
- •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) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •- History of clinical manifestation of any flavivirus infection
- •- History of vaccination against JE (including study participation in any previous or current IC51 clinical study), Yellow fever and Dengue fever
- •- Use of any other investigational or non-registered drug or vaccine in addition to the study vaccine during the study period or within 30 days preceding the first dose of study vaccine
- •- Administration of any other vaccine within 4 weeks before randomization and during the study period
- •- Immunodeficiency including post-organ-transplantation or immunosuppressive therapy
- •- A family history of congenital or hereditary immunodeficiency
- •- History of autoimmune disease
- •- Administration of chronic (defined as more than 14 days) immunosuppressants or other immune-modifying drugs within 6 months of vaccination. (For corticosteroids, this will mean prednisone, or equivalent, >/= 0.05 mg/kg/day. Topical and inhaled steroids are allowed.)
- •- Any acute infections within 4 weeks prior to randomization
- •- History of severe hypersensitivity reactions, in particular to a component of the IC51 vaccine (e.g. protamine sulfate), anaphylaxis or severe cases of atopy requiring emergency treatment or hospital admission
- •- Infection with HIV (a negative test result within 30 days before screening is acceptable), HBV (Hepatitis B surface antigen [HBsAg]) or HCV
- •- History of urticaria after hymenoptera envenomation, drugs, physical or other provocations, or of idiopathic cause
- •- Drug addiction within 6 months prior to enrollment (including alcohol dependence, i.e. more than approximately 60 g alcohol per day, or conditions which might interfere with the study conduct)
- •- Inability or unwillingness to avoid more than the usual intake of alcohol during the 48 hours after vaccination
- •- Diabetes mellitus in subjects receiving insulin therapy, severe cardiopulmonary disorders, or history of malignancy in the past 5 years
- •- Pregnancy (positive pregnancy test during screening or at baseline), lactation or unreliable contraception in female subjects with child-bearing potential (for details, please refer to Section 6.4)
- •- Subjects with any condition which in the opinion of the investigator makes the subject unsuitable for inclusion
- •- Inability or unwillingness to provide informed consent and to abide by the requirements of the study
- •- Persons who have been committed to an institution (by a court or by an authority) will not participate in the study
研究者
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