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临床试验/NCT04688476
NCT04688476进行中(未招募)不适用

An Extended Follow-Up Study of the HPV Vaccine Delayed Booster Trial

University of Arizona2 个研究点 分布在 1 个国家目标入组 113 人开始时间: 2020年11月17日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
113
试验地点
2
主要终点
The differences in geometric mean titer (GMT) of HPV 16 and HPV18 between 30 vs. 48, 48 vs. 60, and 60 vs. 72 months after the priming dose of Gardasil

研究概览

简要总结

This is an extended follow-up study to follow-up study participants who received 1 booster dose of Gardasil 9 in the "HPV vaccine delayed booster trial." This was a prospective, single-arm, open-label, non-randomized, phase IIa trial among 9-11 year-old girls and boys to determine the immunogenicity after a single dose of the nonavalent HPV vaccine (Gardasil 9) over 24 months, with a delayed booster dose at 24 months and an optional booster at 30 months after the first dose. Participants provided blood specimens at 6, 12, 18, 24, and 30 months after the first dose. Serologic geometric mean titers (GMT) of the nine vaccine types (HPV 16/18/ 6/11/31/33/45/52/58) were measured at each time point. One hundred and thirty-three (133) participants received one booster dose at month 24 and elected not to receive the second booster at month 30.

For this follow-up study, we anticipate that we will be able to accrue 120 participants from the original study who received just one booster dose. Participants who received one booster dose of Gardasil 9 will be contacted to return to the clinic to provide blood specimens at 48 (±3), 60 (±3), and 72 (±3) months after the priming dose. Serologic geometric mean titers (GMT) of the nine vaccine types (HPV 16/18/ 6/11/31/33/45/52/58) will be measured at each time point.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Study participants who received one booster dose of Gardasil 9 at month 24 and elected not to receive the second booster at month 30 in the original "HPV vaccine delayed booster trial"
  • Ability to understand and the willingness to sign a written informed consent document by the legal representative(s) of the participant.
  • Ability to understand and the willingness to sign a written assent document by the participant.

排除标准

  • - Has received any HPV vaccine dose from an external source at any point during or after participation in the HPV vaccine delayed booster trial.

结局指标

主要结局

The differences in geometric mean titer (GMT) of HPV 16 and HPV18 between 30 vs. 48, 48 vs. 60, and 60 vs. 72 months after the priming dose of Gardasil

时间窗: 72 months

次要结局

  • The differences in geometric mean titer of other HPV types (HPV6/11/31/33/45/52/58) between 30 vs. 48, 48 vs. 60, and 60 vs. 72 months after the priming dose of Gardasil 9(72 months)

研究者

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

Sherry Chow

Principal Investigator

University of Arizona

研究点 (2)

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