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临床试验/NCT01951677
NCT01951677已完成1 期

Phase 1 Randomized, Controlled, Double-blind Study to Compare the Safety and Effectiveness of Hepatitis B Vaccines in Individuals With Renal Impairment, Diabetes Mellitus or Age Greater Than 40 Years

Vaxine Pty Ltd1 个研究点 分布在 1 个国家目标入组 240 人开始时间: 2013年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
240
试验地点
1
主要终点
Safety

研究概览

简要总结

There is a need for more effective and better-tolerated hepatitis B vaccines for low responder high-risk populations including patients with renal impairment and/or diabetes mellitus and those aged over 40 years. Several approaches are available to enhance the potency of hepatitis B virus vaccines including use of the more highly immunogenic antigens, replacing alum with potentially more effective adjuvants, and increasing the dose of vaccine antigen. A combination of these strategies is being tested in this study to identify the most promising candidate approaches to take forward into advanced clinical development

详细描述

Adjuvants are a critical ingredient in most vaccines and act by boosting the immune response to the target protein (e.g. hepatitis B surface antigen (HBsAg)). Despite considerable research, aluminium hydroxide or phosphate compounds (collectively referred to as "alum") remain the dominant adjuvants used in human hepatitis B virus vaccines. There is thus an unmet need for new HBV vaccine adjuvants, in particular, for adjuvants capable of boosting cell-mediated immunity (this is a particular type of immune response where killer T cells are activated that are then able to attack and destroy the infection) as alum, although good at stimulating antibodies is very poor at stimulating cell-mediated immunity. Alum, whilst generally accepted as safe, can be associated with significant local vaccine reactions and this is another reason why newer better-tolerated vaccine adjuvants would be beneficial. This study will compare a range of experimental adjuvant formulations to identify those that provide the safest and most effective enhancement of T- and B-cell immunity against hepatitis B

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
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18 years and above
  • Male or female
  • Able to provide written informed consent
  • Willing and able to comply with the protocol for the duration of the study.
  • Has one or more of
  • Age 40 years or above
  • Impaired renal function (creatinine >120 mmol/L or calculated glomerular filtration rate <60mls/min)
  • Diagnosis of diabetes mellitus (any type)

排除标准

  • History of prior hepatitis B vaccination
  • History of serious vaccine allergy if in the opinion of the Investigator this represents a contraindication to hepatitis B vaccination
  • Women of childbearing potential unless using a reliable and appropriate contraceptive method, specifically oral contraceptive pill, intrauterine device or mechanical barrier device.
  • Pregnant or lactating women.
  • History of systemic autoimmune disease including Wegener's granulomatosis, systemic lupus erythematosus, Guillain-Barre, scleroderma or multiple sclerosis.
  • Participation in another clinical trial with an investigational agent within 28 days of the scheduled date of first immunization.
  • Any other serious medical, social or mental condition that, in the opinion of the investigator, would be detrimental to the subjects or the study.

研究组 & 干预措施

HBsAg + alum adjuvant

Active Comparator

HBsAg + standard alum adjuvant

干预措施: HBsAg (Drug)

HBsAg + alum adjuvant

Active Comparator

HBsAg + standard alum adjuvant

干预措施: Alum (Biological)

HBsAg + Advax-1(TM)

Experimental

HBsAg + Advax-1

干预措施: HBsAg (Drug)

HBsAg + Advax-1(TM)

Experimental

HBsAg + Advax-1

干预措施: Advax-1(TM) (Biological)

HBsAg + Advax-2(TM)

Experimental

HBsAg + Advax-2

干预措施: HBsAg (Drug)

HBsAg + Advax-2(TM)

Experimental

HBsAg + Advax-2

干预措施: Advax-2(TM) (Biological)

HBsAg + Advax-3(TM)

Experimental

HBsAg + Advax-3

干预措施: HBsAg (Drug)

HBsAg + Advax-3(TM)

Experimental

HBsAg + Advax-3

干预措施: Advax-3(TM) (Biological)

preS HBsAg + alum adjuvant

Active Comparator

preS HBsAg + alum adjuvant

干预措施: PreS HBsAg (Biological)

preS HBsAg + alum adjuvant

Active Comparator

preS HBsAg + alum adjuvant

干预措施: Alum (Biological)

preS HBsAg + Advax-1(TM)

Experimental

preS HBsAg + Advax-1

干预措施: PreS HBsAg (Biological)

preS HBsAg + Advax-1(TM)

Experimental

preS HBsAg + Advax-1

干预措施: Advax-1(TM) (Biological)

preS HBsAg + Advax-2(TM)

Experimental

preS HBsAg + Advax-2

干预措施: PreS HBsAg (Biological)

preS HBsAg + Advax-2(TM)

Experimental

preS HBsAg + Advax-2

干预措施: Advax-2(TM) (Biological)

preS HBsAg + Advax-3(TM)

Experimental

preS HBsAg + Advax-3

干预措施: PreS HBsAg (Biological)

preS HBsAg + Advax-3(TM)

Experimental

preS HBsAg + Advax-3

干预措施: Advax-3(TM) (Biological)

high dose preS HBsAg + alum adjuvant

Active Comparator

high dose preS HBsAg + alum adjuvant

干预措施: PreS HBsAg (Biological)

high dose preS HBsAg + alum adjuvant

Active Comparator

high dose preS HBsAg + alum adjuvant

干预措施: Alum (Biological)

high dose preS HBsAg + Advax-1(TM)

Experimental

high dose preS HBsAg + Advax-1

干预措施: PreS HBsAg (Biological)

high dose preS HBsAg + Advax-1(TM)

Experimental

high dose preS HBsAg + Advax-1

干预措施: Advax-1(TM) (Biological)

high dose preS HBsAg + Advax-2(TM)

Experimental

high dose preS HBsAg + Advax-2(TM)

干预措施: PreS HBsAg (Biological)

high dose preS HBsAg + Advax-2(TM)

Experimental

high dose preS HBsAg + Advax-2(TM)

干预措施: Advax-2(TM) (Biological)

high dose preS HBsAg + Advax-3(TM)

Experimental

high dose preS HBsAg + Advax-3

干预措施: PreS HBsAg (Biological)

high dose preS HBsAg + Advax-3(TM)

Experimental

high dose preS HBsAg + Advax-3

干预措施: Advax-3(TM) (Biological)

结局指标

主要结局

Safety

时间窗: 12 months

Safety as assessed by incidence of adverse events

次要结局

  • Hepatitis B surface antibody geometric mean titer(one-month post each immunization and 10 months post-final immunization)
  • T cell responses(7 days and one month post each immunization and 10 months post-final immunization)
  • Efficacy(one month post each immunization and 10 months post final immunization)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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