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临床试验/NCT05450705
NCT05450705进行中(未招募)3 期

A Phase 3 Open-Label Immunogenicity and Safety Study of 2-Dose Regimens of a 9vHPV Vaccine (V503) in Chinese Girls 9 Through 14 Years of Age With a Comparison to 3-Dose Regimen of V503 in Chinese Women 20 Through 26 Years of Age

Merck Sharp & Dohme LLC2 个研究点 分布在 1 个国家目标入组 1,500 人开始时间: 2022年7月22日最近更新:
适应症

试验速览

阶段
3 期
状态
进行中(未招募)
入组人数
1,500
试验地点
2
主要终点
Stage I: Competitive Luminex immunoassay (cLIA) Geometric Mean Titers (GMTs) to 9 vaccine types of 9vHPV vaccine

研究概览

简要总结

This study aims to demonstrate that a 2-dose regimen of the 9-Valent Human Papillomavirus (9vHPV) vaccine (GARDASIL™9, V503) induces non-inferior competitive Luminex immunoassay (cLIA) geometric mean titers (GMTs) to each of the 9vHPV vaccine types in Chinese girls 9 through 14 years of age compared to a 3-dose regimen in Chinese women 20 through 26 years of age. The primary hypothesis is that a 2-dose regimen has a non-inferiority margin of 0.67 in the GMT ratio (girls vs. women) for each HPV type.

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
None

入排标准

年龄范围
9 Years 至 26 Years(Child, Adult)
性别
Female
接受健康志愿者

入选标准

  • Is a healthy Chinese female.
  • Is not a woman of childbearing potential (WOCBP); or is a WOCBP who has not had sex with males or has had sex with males and used effective contraception during Day 1 through 1 month post last dose.

排除标准

  • Has a history of known prior vaccination with an HPV vaccine.
  • Has a history of severe allergic reaction that required medical intervention.
  • Has a known thrombocytopenia or coagulation disorder that would contraindicate IM injections.
  • Has a history of abnormal Pap test or external genital wart, vulvar intraepithelial neoplasia, vaginal intraepithelial neoplasia, anal intraepithelial neoplasia, vulvar cancer, vaginal cancer, or anal cancer.
  • Has a history of a positive test for HPV.
  • Has received immune globulin or blood-derived products in the past 6 months or plans to receive any before one month post last dose.
  • Has a history of splenectomy, is currently immunocompromised, or has been diagnosed with immunodeficiency, human immunodeficiency virus, lymphoma, leukemia, systemic lupus erythematosus, rheumatoid arthritis, juvenile rheumatoid arthritis, inflammatory bowel disease, or other autoimmune condition.
  • Has received immunosuppressive therapy in the past year, excluding inhaled, nasal, or topical corticosteroids and certain regimens of systemic corticosteroids.

结局指标

主要结局

Stage I: Competitive Luminex immunoassay (cLIA) Geometric Mean Titers (GMTs) to 9 vaccine types of 9vHPV vaccine

时间窗: One month after last dose (Up to Month 13)

cLIA GMT to each of 9 vaccine types of 9vHPV vaccine. The GMT for each HPV type will be reported in mMU/mL.

Stage II: cLIA seropositivity percentages to 9 vaccine types of 9vHPV vaccine in girls 9 through 14 years of age

时间窗: Up to Month 84

cLIA seropositivity to each of 9 vaccine types of 9vHPV vaccine in girls 9 through 14 years of age. The percentage of participants who are seropositive for each HPV type will be summarized.

Stage II: cLIA GMTs to 9 vaccine types of 9vHPV vaccine in girls 9 through 14 years of age

时间窗: Up to Month 84

cLIA GMT to each of 9 vaccine types of 9vHPV vaccine in girls 9 through 14 years of age. The GMT for each HPV type will be reported in mMU/mL.

次要结局

  • Stage I: cLIA seroconversion percentages to 9 vaccine types of 9vHPV vaccine(One month after last dose (Up to Month 13))
  • Stage I: Percentage of participants experiencing solicited systemic AEs(Day 1 through Day 8 following any study vaccination)
  • Stage I: Immunoglobulin G Luminex immunoassay (IgG LIA) GMTs to 9 vaccine types of 9vHPV vaccine at one month post last dose(One month after last dose (Up to Month 13))
  • Stage I: IgG LIA seroconversion percentages to 9 vaccine types of 9vHPV vaccine(One month after last dose (Up to Month 13))
  • Stage I: Percentage of participants experiencing solicited injection-site adverse events (AEs)(Day 1 through Day 8 following any study vaccination)
  • Stage I: Percentage of participants experiencing serious AEs (SAEs) Up to Month 13(Up to Month 13)
  • Stage II: IgG LIA GMTs to 9 vaccine types of 9vHPV vaccine in girls 9 through 14 years of age(Up to Month 84)
  • Stage II: IgG LIA seropositivity percentages to 9 vaccine types of 9vHPV vaccine in girls 9 through 14 years of age(Up to Month 84)
  • Stage II: Percentage of participants experiencing SAEs Up to Month 84(Month 18 up to Month 84)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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