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OpenTrials
Completed

NCT Number: NCT06130345

Post-marketing Safety of Elasomeran/Davesomeran and Andusomeran

The main objective of the study is to evaluate the safety of the elasomeran/davesomeran and andusomeran vaccines as used in routine clinical practice.

Completed

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Key information

Who can participate

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:

  • Non-missing sex: (start of available data, 1 day prior to index)
  • No receipt of elasomeran/davesomeran and andusomeran vaccine: (90 days prior to index, 1 day prior to index)
  • No receipt of influenza vaccine: (90 days prior to index, 1 day prior to index)
  • No receipt of any other COVID-19 vaccine: (90 days prior to index, index date)
  • Continuous enrollment in closed medical and pharmacy claims (365 days prior to index, index date)

Cohort 2: Medically attended COVID-19 concurrent comparator

Eligible vaccine and disease episodes must meet the following inclusion criteria within the specified time windows:

  • Non-missing sex: (start of available data, 1 day prior to index)
  • No receipt of elasomeran/davesomeran and andusomeran vaccine: (180 days prior to index, 1 day prior to index)
  • No evidence of medically attended COVID-19: (180 days prior to index, 1 day prior to index)
  • No receipt of any other COVID-19 vaccine: (180 days prior to index, index date)
  • Continuous enrollment in closed medical and pharmacy claims (365 days prior to index, index date)

Exclusion criteria

  • Vaccine and disease episodes with a prior AESI within the washout window will be excluded from the analytic cohort.
  • For the influenza vaccinated concurrent comparator cohort, individuals who receive an elasomeran/davesomeran and andusomeran vaccine and an influenza vaccine on the same day or within a minimum number of days will be excluded from the primary analysis.

Note: Other protocol-defined inclusion/exclusion criteria may apply.

Treatment and study plan

SPIKEVAX

Biological

Intramuscular injection

Other names: SARS-CoV-2-mRNA vaccine, SPIKEVAX Bivalent, Spikevax XBB.1.5, Elasomeran, Davesomeran, Andusomeran

Primary outcomes

  1. Number of Participants With Adverse Events of Special Interest (AESI)

    Time frame: Day 2 up to Day 60 after vaccination

Sponsors and collaborators

Lead sponsor

ModernaTX, Inc.

Industry

Collaborators

  • Aetion, Inc.

Registry information

Official study title

Post-marketing Safety of Elasomeran/Davesomeran and Andusomeran Vaccines in the United States

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Nov 14, 2023
Registry last updated
Dec 19, 2024

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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