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临床试验/ISRCTN98052401
ISRCTN98052401已完成未知

Studying the immunogenicity and safety of combination vaccines for COVID-19

Asian Healthcare Foundation0 个研究点目标入组 44 人开始时间: 2022年1月6日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
44

研究概览

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Adult male or female human volunteer aged 18-65 years (inclusive of both) and not vaccinated for COVID-19/influenza, willing and able to provide written, signed and dated informed consent
  • 2. Negative immunoglobulin M (IgM) SARS-CoV-2 antibodies through enzyme immunoassay test result
  • 3. Negative COVID-2019 Reverse Transcriptase-Polymerase Chain Reaction (RT-PCR) test result at the screening visit
  • 4. No medical history or evidence of COVID-19
  • 5. No acute infections and/or respiratory diseases within 14 days before enrollment
  • 6. No evidence of vaccine-induced reactions or complications after receiving immunobiological products in the past medical history
  • 7. Willing to give consent to use effective contraception methods during the study
  • 8. Negative urine pregnancy test at the screening visit (for childbearing aged women)
  • 9. Negative human immunodeficiency virus (HIV 1 & 2), syphilis, hepatitis B and C test results

排除标准

  • 1. Aged <18 years of age
  • 2. Any vaccination/immunization within 30 days before enrollment
  • 3. Any treatment with steroids (except hormonal contraceptives) and/or immunoglobulins or other blood products within 30 days before enrollment
  • 4. Any treatment with immunosuppressive therapy within 3 months before enrollment
  • 5. Any drug allergy (anaphylactic shock, Quincke's edema, polymorphic exudative eczema, atopy, serum disease), hypersensitivity or allergic reaction to immunobiological products, known allergic reactions to study drug components, acute exacerbation of allergic diseases on enrollment day
  • 6. Any neoplasms in the past medical history
  • 7. Donated blood or plasma within 3 months before enrollment
  • 8. Any history or evidence of splenectomy
  • 9. Any immunodeficiency state
  • 10. Any history or evidence of anorexia or protein deficiency of any origin
  • 11. Alcohol or drug addiction in the past medical history
  • 12. Participation in any other interventional clinical trial within 3 months
  • 13. Any other condition that the study physician considers as a barrier to the trial completion as per the protocol
  • 14. Pregnancy or breastfeeding
  • 15. Subjects who test positive for Coronavirus disease through RT-PCR SARS CoV-2 Test and positive anti-COVID antibodies

研究者

发起方
Asian Healthcare Foundation

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