A Single-center, Randomized, Double-blind, and Placebo Controlled Phase Ⅰ Clinical Trial of the Safety and Preliminary Immunogenicity of Enterovirus Type71 - Coxsackievirus Type A16 Bivalent Vaccine in People Aged 6 Months to 59 Years
试验速览
- 阶段
- 1 期
- 状态
- 尚未招募
- 入组人数
- 144
- 试验地点
- 1
- 主要终点
- Safety index - incidence of adverse events
研究概览
简要总结
This is a randomized, double-blinded, placebo-controlled phase I clinical trial to evaluate the safety and preliminary immunogenicity of the Enterovirus Type71 - Coxsackievirus Type A16 bivalent vaccine in subjects ( aged 6 months to 59 years ).
详细描述
This is a single-center, randomized, double-blinded, placebo-controlled phase I clinical trial in which three dose levels of the Enterovirus Type71 -Coxsackievirus Type A16 bivalent vaccine will be evaluated the safety and preliminary immunogenicity in subjects aged 6 months to 59 years. A total of 144 participants will be enrolled, including 48 adults (aged 18-59 years), 48 adolescents (aged 6-17 years), and 48 children (aged 6 months-5 years). Participants will be randomized into vaccine group and placebo group in a 3:1 ratio, and receive two doses of vaccine or placebo according to the 0- and 28-day immunization schedule.The dose escalation principle within each age group is from low to high doses, and the sequential enrollment principle between different age groups is from adults to children.
Primary endpoints are the occurrence of safety events after vaccination including the incidence of adverse events within 30 minutes/7 days/28 days after each dose, as well as the incidence of serious adverse events within 12 months after the final dose which will be defined as the secondary safety endpoint. Besides, the secondary immunogenicity endpoints are the geometric mean titers, geometric mean fold increases, seropositive rates, and seroconversion rates of anti-EV71 neutralizing antibodies and anti-CA16 neutralizing antibodies 28 days after the final dose.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Sequential
- 主要目的
- Prevention
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 6 Months 至 59 Years（Child, Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Age Requirement: volunteers aged 6 months and 59 years.
- •Provision of Legal Identification: volunteers and their legal guardians or appointed representatives must provide valid legal identification documents.
- •Informed Consent: participants, legal guardians, or appointed representatives of volunteers must have the capacity to understand the informed consent document and the research process, voluntarily participate, sign the informed consent form, and be able to comply with the requirements in the study as well as complete relevant visits on time.
- •6~23months old: term delivery (gestational week 37 weeks ~ 42 weeks at birth), 2500g ≤ birth weight ≤ 4000g.
- •Requirements for contraception: agree to take contraception actions in 12 months.
- •Temperature Requirement: axillary body temperature is less than 37.3°C.
排除标准
- •Subjects meeting any of the following exclusion criteria will be not eligible for enrollment.
- •Subjects who have been allergic to any component of the vaccine in the past, or have any history of vaccine allergy or suspected allergy or other serious adverse reactions, such as urticaria, respiratory distress, and angioedema.
- •History of taking administration of a non-SARS-CoV-2 inactivated vaccine or subunit vaccine within 7 days before enrollment, or any live attenuated vaccine or SARS-CoV-2 vaccine within 14 days before enrollment.
- •Subjects with convulsion, epilepsy, encephalopathy, psychiatric history or family history.
- •Known to have serious congenital malformations, developmental disorders, genetic defects or abnormal growth and development, or clinically diagnosed serious chronic diseases, including but not limited to neurological, cardiovascular, blood and lymphatic system, immune system, kidney, liver, gastrointestinal, respiratory system, metabolism and bone diseases and a history of malignant tumors.
- •Subjects are acutely ill or in the acute phase of a chronic illness within 3 days before vaccination.
- •Subjects with a hereditary bleeding tendency or coagulopathy, or a history of bleeding disorders.
- •Subjects who intolerance to venipuncture and with a history of needle- or blood-induced syncope.
- •History of surgical removal of the spleen or other vital organs for any reason.
- •Donation or loss of blood (≥400 mL), receipt of blood products, or receipt of blood transfusion within the 3 months before enrollment.
- •Use of any investigational or unregistered product (drug, vaccine, biological product, or device) other than a study vaccine within 3 months before enrollment or planned for use during the study.
- •Have treatment with immunosuppressive agents within 6 months before enrollment, such as long-term systemic glucocorticoid therapy (e.g., prednisone or a similar drug for more than 2 consecutive weeks within 6 months), but topical use (e.g., ointments, eye drops, inhalers, or nasal sprays) was allowed. Topical use should not exceed the recommended dose on the label or have any signs of systemic exposure.
- •History of any EV71 antigen-containing vaccination, whether commercially available or investigational.
- •Subjects with history of hand, foot, and mouth disease.
- •Subjects with abnormal vital signs with clinical significance.
- •Subjects who do not meet the criteria for good health based on comprehensive physical examination, including: (1) abnormal vital signs with clinical significance; (2) clinical laboratory testing shows laboratory abnormalities and with clinical significance (applicable only to subjects aged 2 years and above).
- •Have been diagnosed with an infectious disease that may interfere with the conduct or completion of the study, such as active tuberculosis, viral hepatitis, human immunodeficiency virus (HIV) infection, etc.
- •Females with positive pregnancy test results.
- •Females who are lactating, or subjects who plan to conceive or to donate sperm or ova from the time of signing the informed consent form until 12 months after completion of the full vaccination schedule (applicable only to subjects aged 18 to 59 years).
- •Subjects with a history of abnormal birth delivery, birth asphyxia, neurological impairment, or clinically diagnosed pathological jaundice (applicable only to subjects aged 6 to 23 months).
- •Subjects deemed by the investigator to be unsuitable for participation in the study.
研究组 & 干预措施
low-dose experimental group
Participants aged 18~59 years old, 6~17years old, 6months old~5 years old
干预措施: Low Dose Enterovirus Type71 - Coxsackievirus Type A16 bivalent vaccine, inactivated (human diploid cell) (Biological)
medium-dose experimental group
Participants aged 18~59 years old, 6~17years old, 6months old~5 years old
干预措施: Medium Dose Enterovirus Type71 - Coxsackievirus Type A16 bivalent vaccine, inactivated (human diploid cell) (Biological)
high-dose experimental group
Participants aged 18~59 years old, 6~17years old, 6months old~5 years old
干预措施: High Dose Enterovirus Type71 - Coxsackievirus Type A16 bivalent vaccine, inactivated (human diploid cell) (Biological)
Placebo control group
Participants aged 18~59 years old, 6~17years old, 6months old~5 years old
干预措施: Placebo (Biological)
结局指标
主要结局
Safety index - incidence of adverse events
时间窗: 0- 30 minutes/Day 0 to 7 days/Day 0 to 28 days after each dose
Incidence of adverse events after each dose vaccination
次要结局
- Safety index - incidence of serious adverse events(From the beginning of the vaccination up to12 months after the last vaccination completed)
- Immunogenicity index-Seroconversion rates(Between baseline and Day 28 after full vaccination)
- Immunogenicity index - Geometric mean titer (GMT)(Day 28 after full vaccination)
- Immunogenicity index - Geometric mean fold increases (GMFI)(Between baseline and Day 28 after full vaccination)
- Immunogenicity index-Seropositive rates(Day 28 after full vaccination)