• sponsor
    Emergent BioSolutions
Updated on 13 January 2022


The goal of this multi-center, randomized, double blind, placebo controlled study is to evaluate the safety and immunogenicity of PXVX0317 in healthy adult and adolescent subjects.


  • Condition: Chikungunya
  • Clinical Trial Identifier: NCT05072080
  • Sponsor: Emergent BioSolutions

Condition Vaccines
Clinical Study IdentifierTX290578
SponsorEmergent BioSolutions
Last Modified on13 January 2022


Yes No Not Sure

Inclusion Criteria

Males or females, 12 to <65 years of age
Able and willing to provide informed consent (and assent, as applicable) voluntarily signed by subject (and guardian, as applicable)

Exclusion Criteria

Currently pregnant, breastfeeding, or planning to become pregnant during the study
Positive laboratory evidence of current infection with human immunodeficiency virus (HIV-1, HIV-2), hepatitis C virus (HCV) or hepatitis B virus (HBV)
History of severe allergic reaction or anaphylaxis to any component of the vaccine
History of any known congenital or acquired immunodeficiency that could impact response to vaccination (e.g., leukemia, lymphoma, generalized malignancy, functional or anatomic asplenia, alcoholic cirrhosis)
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Step 1 Connect with a study center
What happens next?
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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