A Study to Investigate Safety, Reactogenicity, and Immunogenicity of mRNA-1365 (Profile 2) in Older Healthy Adults

NCT07764237 · Status: NOT_YET_RECRUITING · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 375

Last updated 2026-08-13

No results posted yet for this study

Summary

The main objective of this trial is to evaluate the safety, reactogenicity, and immunogenicity of study interventions across intervention groups

Conditions

  • Respiratory Syncytial Virus (RSV)
  • Human Metapneuomovirus (hMPV)

Interventions

BIOLOGICAL

mRNA-1365 (Profile 2)

Sterile liquid for injection

BIOLOGICAL

mRNA-1345 (Profile 1)

Sterile liquid for injection

BIOLOGICAL

mRNA-1345 (Profile 3)

Sterile liquid for injection

Sponsors & Collaborators

  • ModernaTX, Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
SEQUENTIAL

Eligibility

Min Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-08-16
Primary Completion
2027-07-20
Completion
2027-07-20
FDA Drug
Yes

Countries

  • Canada
  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07764237 on ClinicalTrials.gov