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 == Clinical Trials Summary == == Clinical Trials Summary ==
  
-|  |   Participants   |   Covid +   |   Total Adverse Events   |   # of Solicited Severe Adverse Events Reported   |    # of Vax Related Serious  Adverse Events  |   Observed AE's   |  +|  |   Participants   |   Covid+   |   Total Adverse Events   |   # of Solicited Severe Adverse Events Reported   |    # of Vax Related Serious  Adverse Events  |   Observed AE's   |  
-|Phase 1/2|   153   |   2   |   27   |   2   |   0   | pain, tenderness, erythema, induration/swelling, nausea/vomiting, headache, fatigue, myalgia, neutropenia, eosinophilia, thrombocytopenia, chilblains, haematuria, rise in red blood cell/erythrocyte sedimentation rate,   | +|Phase1/2|   153   |   2   |   106   |   2   |   0   | pain, tenderness, erythema, induration/swelling, nausea/vomiting, headache, fatigue, myalgia, neutropenia, eosinophilia, thrombocytopenia, chilblains, haematuria, rise in red blood cell/erythrocyte sedimentation rate   | 
-|Phase 3 |   4,012   |   ?   |   ?   |   0   |+|Phase3 |   4,012   |   ?   |   ?   |   0   |
  
 == Published Clinical Trial Results ==  == Published Clinical Trial Results == 
-[[https://www.medrxiv.org/content/10.1101/2021.08.13.21262021v2|Immunogenicity and safety of inactivated whole virion Coronavirus vaccine with CpG (VLA2001) in healthy adults aged 18 to 55: a randomised phase 1 /2 clinical trial]]+[[https://www.medrxiv.org/content/10.1101/2021.08.13.21262021v2|NCT04671017: Immunogenicity and safety of inactivated whole virion Coronavirus vaccine with CpG (VLA2001) in healthy adults aged 18 to 55: a randomised phase 1 /2 clinical trial]]
  
 +{{https://www.medrxiv.org/content/medrxiv/early/2021/08/20/2021.08.13.21262021/T3.medium.gif}}
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 +== Registered Clinical Trials ==
   NCT04671017 Dose Finding Study to Evaluate Safety, Tolerability and Immunogenicity of an Inactiviated Adjuvanted Sars-Cov-2 Virus Vaccine Candidate Against Covid-19 in Healthy Adults.    NCT04671017 Dose Finding Study to Evaluate Safety, Tolerability and Immunogenicity of an Inactiviated Adjuvanted Sars-Cov-2 Virus Vaccine Candidate Against Covid-19 in Healthy Adults. 
   NCT04864561 Study To Compare The Immunogenicity Against COVID-19, Of VLA2001 Vaccine To AZD1222 Vaccine (COV-COMPARE).    NCT04864561 Study To Compare The Immunogenicity Against COVID-19, Of VLA2001 Vaccine To AZD1222 Vaccine (COV-COMPARE). 
   NCT04956224 Immunogenicity of VLA2101 Compared to VLA2001.    NCT04956224 Immunogenicity of VLA2101 Compared to VLA2001. 
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