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临床试验/NCT00662870
NCT00662870已完成3 期

Safety, Immunogenicity and Lot Comparability of DAPTACEL™ (Aventis Pasteur Classic Five-component Pertussis Vaccine in Combination With Tetanus and Diphtheria Toxoids Adsorbed) When Administered With Other Recommended Vaccines at 2, 4, 6, and 15 to 16 Months of Age.

Sanofi26 个研究点 分布在 1 个国家目标入组 1,941 人开始时间: 2001年5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
Sanofi
入组人数
1,941
试验地点
26
主要终点
Immunogenicity: To provide information concerning the immune response of DAPTACEL after vaccination.

研究概览

简要总结

This study was designed to assess the lot comparability of DAPTACEL, as well as the safety and immunogenicity of DAPTACEL when co-administered with other recommended infant vaccines.

Stage I Primary Objectives:

  1. To assess the lot-comparability of immunogenicity of DAPTACEL by when co-administered with other recommended vaccines.
  2. To compare the immune response to DTaP-IPV/Hib (Pentacel) with those of three lots of DAPTACEL when co-administered with other recommended vaccines.
  3. To compare the immune response of PRP-T antigen in Pentacel with that of ActHIB concurrently administered in a different injection site with DAPTACEL when these vaccines are co-administered with other recommended vaccines.

Stage II Primary Objectives:

  1. To compare the immune response of DAPTACEL when the 4th dose is co-administered with Hib or other infant vaccines.
  2. To compare the the immune response of Pentacel with those elicited by DAPTACEL when co-administered with ActHIB in toddlers.

详细描述

This is a two-stage, randomized, multi-center study to assess the safety, immunogenicity and lot comparability of DAPTACEL

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
42 Days 至 84 Days(Child)
性别
All
接受健康志愿者
是

入选标准

  • •Healthy infants 2 months of age.
  • •Infants with at least 37 weeks of gestation at delivery.
  • •Signed informed consent from parent or guardian.
  • •Able to attend the scheduled visits and to comply with the study procedure.
  • •Subjects must have received the first dose of hepatitis B vaccine from birth to 28 days prior to the first dose of DAPTACEL or Pentacel.

排除标准

  • •Clinically significant findings on review of systems or physical examination (determined by investigator or sub-investigator to be sufficient for exclusion).
  • •Known or suspected hypersensitivity to any component of the study vaccine to be administered.
  • •Known or suspected impairment of immunologic function or receipt of immunosuppressive therapy or immunoglobulin since birth.
  • •Known HIV-positive mother.
  • •Personal or immediate family history of congenital immune deficiency.
  • •Developmental delay or neurologic disorders.
  • •Chronic medical, congenital, developmental or surgical disease.
  • •Participation in any other experimental vaccine trial.
  • •Any condition which, in the opinion of the investigator or sub-investigator, would interfere with the evaluation of the vaccine or pose a health risk to the subject.
  • •Prior history of having received more than one dose of hepatitis B vaccine, any diphtheria, tetanus and acellular pertussis combination vaccine (DTaP), diphtheria, tetanus and whole-cell pertussis combination vaccine (DTwP), Haemophilus influenzae type b (Hib)-conjugate vaccine, poliovirus vaccine or pneumococcal conjugate vaccine

研究组 & 干预措施

DAPTACEL Lot 1

Experimental

Participants receiving Diphtheria and Tetanus Toxoids and Acellular Pertussis vaccine (DAPTACEL) Lot 1

干预措施: DAPTACEL® (Diphtheria and Tetanus Toxoids and Acellular Pertussis vaccine) (Biological)

DAPTACEL Lot 2

Experimental

Participants receiving Diphtheria and Tetanus Toxoids and Acellular Pertussis vaccine (DAPTACEL) Lot 2

干预措施: DAPTACEL® (Diphtheria and Tetanus Toxoids and Acellular Pertussis vaccine) (Biological)

DAPTACEL Lot 3

Experimental

Participants receiving Diphtheria and Tetanus Toxoids and Acellular Pertussis vaccine (DAPTACEL) Lot 3

干预措施: DAPTACEL® (Diphtheria and Tetanus Toxoids and Acellular Pertussis vaccine) (Biological)

Pentacel

Active Comparator

Participants receiving Pentacel vaccine

干预措施: Pentacel: DTaP-IPV/Hib (Biological)

结局指标

主要结局

Immunogenicity: To provide information concerning the immune response of DAPTACEL after vaccination.

时间窗: 30 days post-vaccination 3

次要结局

未报告次要终点

研究者

发起方
Sanofi
申办方类型
Industry
责任方
Sponsor

研究点 (26)

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