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Post-marketing Surveillance (PMS) Use-Result Surveillance With SPIKEVAX BIVALENT, SPIKEVAX X Injection, SPIKEVAX JN Injection and SPIKEVAX IN PRE-FILLED SYRINGE

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NCT06333704 · readout in 953 d

Sponsored by ModernaTX, Inc. (industry) · MRNA — their whole pipeline →. With C&R Research, Inc..

Phase
Status
Active, not recruiting
Study type
Observational
Enrollment
4,207actual
Sites
26
Country
South Korea

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2023-03-10actualWhen the study began enrolling
Primary completion2029-03-29estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2029-03-29estimatedThe whole study's end, after follow-up
First posted2024-03-27actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-04-16actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • SARS-CoV-2

Interventions

  • Biological: SPIKEVAX Bivalent BA.1 — also filed as MODERNA SPIKEVAX BIVALENT (Elasomeran, Imelasomeran), SPIKEVAX BIVALENT (Elasomeran, Imelasomeran)
  • Biological: SPIKEVAX Bivalent BA.4/5 — also filed as SPIKEVAX BIVALENT (Elasomeran, Davesomeran), SPIKEVAX BIVALENT INJECTION DUO (Elasomeran, Davesomeran)
  • Biological: SPIKEVAX XBB.1.5 — also filed as SPIKEVAX X Injection
  • Biological: SPIKEVAX JN.1 — also filed as SPIKEVAX JN Injection, SPIKEVAX in Pre-filled Syringe

Primary outcome

what the primary-completion date above is the date OF
Number of Participants With AEs
measured Up to 28 days post vaccination

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