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临床试验/NCT00518180
NCT00518180已完成3 期

A Phase 3, Single-Center, Open-label, Controlled, Randomized Study to Evaluate the Safety and Immunogenicity of Novartis Men ACWY Vaccine Administered Either Alone or Concomitantly With a Combined Tetanus, Reduced Diphtheria Toxoid, Acellular Pertussis Vaccine and Quadrivalent Human Papillomavirus [Types 6, 11, 16, 18] Recombinant Vaccine in Healthy Adolescents

Novartis Vaccines1 个研究点 分布在 1 个国家目标入组 1,620 人开始时间: 2007年7月1日最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
1,620
试验地点
1
主要终点
Percentage of Subjects With Human Serum Bactericidal Assay (hSBA) Seroresponse

研究概览

简要总结

This study will evaluate the safety and immune response of the Novartis Meningococcal ACWY conjugate vaccine when administered with Tdap and HPV vaccinations to healthy adolescents

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
11 Years 至 18 Years(Child, Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Healthy adolescents 11-18 years of age
  • •virgins (both male and female) with no intention of becoming sexually active during the study period
  • •who have been properly vaccinated against diphtheria, tetanus, pertussis

排除标准

  • •who had a previous confirmed or suspected disease caused by N. meningitidis;
  • •who have previously been immunized with a meningococcal vaccine
  • •who have received prior human papillomavirus (HPV) vaccine;
  • •who have any serious acute, chronic or progressive disease
  • •who have epilepsy, any progressive neurological disease or history of Guillain-Barre syndrome;
  • •who have a known or suspected impairment/alteration of immune function, either congenital or acquired
  • •who are known to have a bleeding diathesis, or any condition that may be associated with a prolonged bleeding time;
  • •who have Down's syndrome or other known cytogenic disorders;

研究组 & 干预措施

MenACWY + Tdap + HPV

Experimental

Subjects received MenACWY concomitantly with Tdap and HPV at study month 0 followed by two injections of HPV at month 2 and 6

干预措施: Novartis Meningococcal ACWY Conjugate Vaccine (Biological)

MenACWY →Tdap → HPV

Experimental

Subjects received MenACWY at study month 0 followed by one injection of Tdap at month 1, followed by three injections of HPV at months 2, 4, and 8

干预措施: Novartis Meningococcal ACWY Conjugate Vaccine (Biological)

Tdap →MenACWY → HPV

Experimental

Subjects received Tdap at month 0 followed by one injection of MenACWY at month 1, followed by three injections of HPV at months 2, 4, and 8

干预措施: Tdap Vaccine (Biological)

结局指标

主要结局

Percentage of Subjects With Human Serum Bactericidal Assay (hSBA) Seroresponse

时间窗: 1 month post MenACWY vaccination

Immune responses to MenACWY, as measured by the percentage of hSBA seroresponders, when given: (a) alone; (b) concomitantly with a Tetanus diphtheria acellular pertussis (Tdap) vaccine and a Human Papillomavirus Recombinant (HPV) vaccine; and (c) when given one month after a Tdap vaccine. Seroresponse to MenACWY: For a subject with baseline hSBA titer \<1:4, seroresponse is defined as a postvaccination hSBA titer ≥ 1:8; for a subject with baseline hSBA titer ≥ 1:4, seroresponse is defined as a postvaccination hSBA titer of at least 4 times the baseline.

Percentage of Subjects With Antidiphtheria and Antitetanus Toxin ≥1.0 IU/mL

时间窗: 1 month post Tdap vaccination

To compare the immune response to Tdap given concomitantly with MenACWY and HPV vaccine with the immune response to Tdap when administered alone

Geometric Mean Concentrations (GMC) of Antipertussis Toxin (Anti-PT), Antifilamentous Hemagglutinin (Anti-FHA), and Antipertactin (Anti-PRN)

时间窗: 1 month post Tdap vaccination

To compare the immune response of Tdap given concomitantly with MenACWY and HPV vaccine with the immune response of Tdap when administered alone

次要结局

  • Effect of Concomitant and Sequential Vaccination on hSBA Geometric Mean Titers (GMTs) for A, C, W, and Y Serogroups(1 month post MenACWY vaccination)
  • Percentage of Subjects With Anti-HPV Seroconversion(1 month post third HPV vaccination)
  • The Effect of Sequential Vaccination on Immunogenicity for Diphtheria and Tetanus(1 month post Tdap vaccination)
  • Geometric Mean Concentrations (GMC) for Diphtheria and Tetanus(1 month post Tdap vaccination)
  • Geometric Mean Titers (GMT) of Pertussis Antigens(1 month post Tdap vaccination)
  • Percentages of Subjects With at Least a 4-fold Rise for PT, FHA, and PRN(1 month post Tdap vaccination)
  • Percentage of Subjects With hSBA ≥ 1:8, hSBA Titer ≥ 1:4, for A, C, W, and Y Serogroups(1 month post MenACWY vaccination)
  • Geometric Mean Titers (GMTs) of Anti-HPV by Competitive Luminex Immunoassay(1 month post third HPV vaccination)
  • Number of Subjects With at Least One Reactogenicity Sign After MenACWY and Tdap Vaccination.(Days 1 to 7)
  • Number of Subjects With at Least One Reactogenicity Sign After Each HPV Vaccination(Days 1 to 7)

研究者

发起方
Novartis Vaccines
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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