Aetion, Inc
New York, 10001, United States
NCT Number: NCT06130345
The main objective of the study is to evaluate the safety of the elasomeran/davesomeran and andusomeran vaccines as used in routine clinical practice.
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Observational
New York, 10001, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Cohort 1: Influenza vaccinated concurrent comparator
Eligible vaccine episodes must meet the following inclusion criteria within the protocol-specified time windows:
Cohort 2: Medically attended COVID-19 concurrent comparator
Eligible vaccine and disease episodes must meet the following inclusion criteria within the specified time windows:
Exclusion criteria
Note: Other protocol-defined inclusion/exclusion criteria may apply.
Intramuscular injection
Other names: SARS-CoV-2-mRNA vaccine, SPIKEVAX Bivalent, Spikevax XBB.1.5, Elasomeran, Davesomeran, Andusomeran
Time frame: Day 2 up to Day 60 after vaccination
ModernaTX, Inc.
Industry
Post-marketing Safety of Elasomeran/Davesomeran and Andusomeran Vaccines in the United States
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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