Pneumococcal Infection

  • STATUS
    Recruiting
  • sponsor
    Merck Sharp & Dohme Corp.
Updated on 18 April 2022
covid-19
polysaccharide

Summary

The purpose of this study is to evaluate the concomitant and non-concomitant use of messenger ribonucleic acid (mRNA) mRNA-1273, the nucleoside-modified mRNA vaccine for active immunization to prevent coronavirus disease (COVID-19) caused by severe acute respiratory syndrome coronavirus (SARS-CoV-2), with a 23-valent pneumococcal polysaccharide vaccine for the prevention of pneumococcal disease (V110) and, a 15-valent pneumococcal conjugate vaccine (PCV) indicated for the prevention of invasive pneumococcal disease (V114).

Description

  • Condition: Pneumococcal Infection
  • Clinical Trial Identifier: NCT05158140
  • Sponsor: Merck Sharp & Dohme Corp.
Looking for participants within a 30 mile radius of the study site.

Details
Condition Pneumonia
Clinical Study IdentifierTX290674
SponsorMerck Sharp & Dohme Corp.
Last Modified on18 April 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Age 50+
Is in good health. Any underlying chronic illness must be documented to be in stable condition
Has received a 2-dose regimen of the Moderna mRNA SARS-CoV-2 vaccine ≥6 months before enrollment

Exclusion Criteria

Has a current or known history of SARS-CoV-2 infection
Has a history of myocarditis and/or pericarditis
Has a known or suspected impairment of immunological function including, but not limited to, a history of congenital or acquired immunodeficiency, documented human immunodeficiency virus (HIV) infection, functional or anatomic asplenia, or history of autoimmune disease
Has a coagulation disorder contraindicating intramuscular vaccinations
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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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