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临床试验/NCT05329961
NCT05329961进行中(未招募)早期 1 期

An Open-Label Clinical Trial Evaluating the Immunogenicity of the 9vHPV Vaccination 2-dose Regimen Over a Four-year Follow up Among Children 4 to 8 Years Old, An Exploratory Immunogenicity Study

Boston Medical Center1 个研究点 分布在 1 个国家目标入组 155 人开始时间: 2022年9月26日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
早期 1 期
状态
进行中(未招募)
入组人数
155
试验地点
1
主要终点
HPV11 antibodies at 60 months

研究概览

简要总结

This study is an open-label nonrandomized exploratory proof of concept and descriptive 4-year immunogenicity study to assess immunogenicity after administration of a 2-dose regimen of 9-valent human papillomavirus vaccine (9vHPV) vaccine separated by 12 months (months 0, 12).

详细描述

Study participants will include 150 boys and girls aged 4-8 years (total, 75 boys and 75 girls) to receive 2 doses of the 9vHPV vaccine at 0 and 12 months. Patients will be recruited by age-group to achieve balanced enrollment of 15 girls and 15 boys per year of age. The investigators will examine the immunogenicity profile in this cohort, for which titers will be analyzed one month after dose 2 (Month 13).

Though clinical efficacy cannot be assessed in young children because of limited exposure to human papillomavirus (HPV), this descriptive study will allow the investigators to understand whether the 9vHPV vaccine in younger patients provides immunogenicity similar to that shown for the 9-14 and 16-26 age groups who have received the 9vHPV vaccine. This study will require an IND for the use of the HPV vaccine in children younger than 9 years.

Immunogenicity will be measured by examining serum antibodies of all participants using a competitive Luminex immunoassay (cLIA). The antibody response testing will be performed at Merck Research Laboratory.

The goal of this study is to explore whether a 2-dose 9vHPV vaccine regimen with dosage separated by 12 months is immunogenic among children aged 4-8 years. The primary outcome will be geometric mean titers (GMT) for HPV6, HPV11, HPV16, HPV18, HPV31, HPV33, HPV45, HPV52, and HPV58 antibodies at month 13. Results will allow the investigators to qualitatively compare immunogenicity in individuals vaccinated at age 4-8 years to known immunogenicity in 9vHPV recipients vaccinated at ages 9-14. Knowledge of whether vaccination in this age group is sufficient to induce high-level protective antibody titers after the second dose will support further efficacy studies in a larger randomized trial of a 2-dose 9vHPV regimen for children aged 4-8 years.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
4 Years 至 8 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Children aged 4-8 years old
  • Receives care at the Boston Medical Center or one of the affiliated Community heath centers
  • Naïve to HPV Vaccine

排除标准

  • A history of severe allergic reaction, including known allergy to any vaccine component, specially severe allergic reaction to yeast
  • Immunocompromised/previous immunosuppressive therapy
  • Thrombocytopenia or other coagulation disorder

研究组 & 干预措施

Single Arm

Experimental

HPV 9-valent human papillomavirus vaccine (Gardasil 9) - 0.5mL intramuscular dose - 2 doses (Month 0, 12)

干预措施: Gardasil9 (Drug)

结局指标

主要结局

HPV11 antibodies at 60 months

时间窗: 60 months

A serum sample will be analyzed using 9-valent Luminex immunoassay (cLIA, mMU/mL) to assess the geometric mean for HPV antibodies. The results will be considered positive for HPV11 if it is \>16 mMU.

HPV18 antibodies at 13 months

时间窗: 13 months

A serum sample will be analyzed using 9-valent Luminex immunoassay (cLIA, mMU/mL) to assess the geometric mean for HPV antibodies. The results will be considered positive for HPV18 if it is \>24 mMU.

HPV31 antibodies at 13 months

时间窗: 13 months

A serum sample will be analyzed using 9-valent Luminex immunoassay (cLIA, mMU/mL) to assess the geometric mean for HPV antibodies. The results will be considered positive for HPV31 if it is \>10 mMU.

HPV33 antibodies at 13 months

时间窗: 13 months

A serum sample will be analyzed using 9-valent Luminex immunoassay (cLIA, mMU/mL) to assess the geometric mean for HPV antibodies. The results will be considered positive for HPV33 if it is \>8 mMU.

HPV45 antibodies at 13 months

时间窗: 13 months

A serum sample will be analyzed using 9-valent Luminex immunoassay (cLIA, mMU/mL) to assess the geometric mean for HPV antibodies. The results will be considered positive for HPV45 if it is \>8 mMU.

HPV52 antibodies at 13 months

时间窗: 13 months

A serum sample will be analyzed using 9-valent Luminex immunoassay (cLIA, mMU/mL) to assess the geometric mean for HPV antibodies. The results will be considered positive for HPV52 if it is \>8 mMU.

HPV58 antibodies at 13 months

时间窗: 13 months

A serum sample will be analyzed using 9-valent Luminex immunoassay (cLIA, mMU/mL) to assess the geometric mean for HPV antibodies. The results will be considered positive for HPV58 if it is \>8 mMU.

HPV6 antibodies at 60 months

时间窗: 60 months

A serum sample will be analyzed using 9-valent Luminex immunoassay (cLIA, mMU/mL) to assess the geometric mean for HPV antibodies. The results will be considered positive for HPV6 if it is \>30mMU.

HPV16 antibodies at 60 months

时间窗: 60 months

A serum sample will be analyzed using 9-valent Luminex immunoassay (cLIA, mMU/mL) to assess the geometric mean for HPV antibodies. The results will be considered positive for HPV16 if it is \>20 mMU.

HPV18 antibodies at 60 months

时间窗: 60 months

A serum sample will be analyzed using 9-valent Luminex immunoassay (cLIA, mMU/mL) to assess the geometric mean for HPV antibodies. The results will be considered positive for HPV18 if it is \>24mMU.

HPV31 antibodies at 60 months

时间窗: 60 months

A serum sample will be analyzed using 9-valent Luminex immunoassay (cLIA, mMU/mL) to assess the geometric mean for HPV antibodies. The results will be considered positive for HPV31 if it is \>10 mMU.

HPV33 antibodies at 60 months

时间窗: 60 months

A serum sample will be analyzed using 9-valent Luminex immunoassay (cLIA, mMU/mL) to assess the geometric mean for HPV antibodies. The results will be considered positive for HPV33 if it is \>8 mMU.

HPV45 antibodies at 60 months

时间窗: 60 months

A serum sample will be analyzed using 9-valent Luminex immunoassay (cLIA, mMU/mL) to assess the geometric mean for HPV antibodies. The results will be considered positive for HPV45 if it is \>8 mMU.

HPV52 antibodies at 60 months

时间窗: 60 months

A serum sample will be analyzed using 9-valent Luminex immunoassay (cLIA, mMU/mL) to assess the geometric mean for HPV antibodies. The results will be considered positive for HPV52 if it is \>8 mMU.

HPV58 antibodies at 60 months

时间窗: 60 months

A serum sample will be analyzed using 9-valent Luminex immunoassay (cLIA, mMU/mL) to assess the geometric mean for HPV antibodies. The results will be considered positive for HPV58 if it is \>8 mMU.

HPV6 antibodies at 13 months

时间窗: 13 months

A serum sample will be analyzed using 9-valent Luminex immunoassay (cLIA, mMU/mL) to assess the geometric mean for HPV antibodies. The results will be considered positive for HPV6 if it is \>30mMu.

HPV11 antibodies at 13 months

时间窗: 13 months

A serum sample will be analyzed using 9-valent Luminex immunoassay (cLIA, mMU/mL) to assess the geometric mean for HPV antibodies. The results will be considered positive for HPV11 if it is \>16mMu.

HPV16 antibodies at 13 months

时间窗: 13 months

A serum sample will be analyzed using 9-valent Luminex immunoassay (cLIA, mMU/mL) to assess the geometric mean for HPV antibodies. The results will be considered positive for HPV16 if it is \>20mMu.

次要结局

  • Injection site swelling after first injection(day 3 after injection)
  • Injection site swelling after second injection(day 3 after injection)
  • Injection site redness after first injection(day 3 after injection)
  • Injection site redness after second injection(day 3 after injection)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Eilsha Wachman

Professor of Pediatrics, Vice Chair for Research

Boston Medical Center

研究点 (1)

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