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A Study to Evaluate the Safety, Reactogenicity, and Immunogenicity of mRNA-1982 to Prevent Lyme Disease in Healthy Participants (18 to 70 Years of Age)

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NCT07561294 · readout in 812 d

Sponsored by ModernaTX, Inc. (industry) · MRNA — their whole pipeline →.

Phase
Phase 2
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · Single · Prevention
Enrollment
366actual
Sites
8
Country
Canada

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
Start2026-04-29actualWhen the study began enrolling
Primary completion2028-11-09estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2028-11-09estimatedThe whole study's end, after follow-up
First posted2026-05-01actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-03actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Lyme Disease

Interventions

  • Biological: mRNA-1982
  • Biological: Placebo

Primary outcomes

what the primary-completion date above is the date OF
Both Phases: Number of Participants with Solicited Local and Systemic Adverse Reactions
measured Day 1 up to Day 7 (7 days post-injection)
Both Phases: Number of Participants with Unsolicited Adverse Events
measured Day 1 up to Day 28 (28 days post-injection)
Both Phases: Number of Participants with Medically Attended Adverse Events, Adverse Events of Special Interest, Serious Adverse Events, and Adverse Events Leading to Discontinuation
measured Day 1 up to Month 21 (End of study)

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