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NCT05585632 · ClinicalTrials.gov registry record · Phase 1

A Safety, Reactogenicity, and Immunogenicity Study of mRNA-1045 (Influenza and Respiratory Syncytial Virus [RSV]) or mRNA-1230 (Influenza, RSV, and Severe Acute Respiratory Syndrome Coronavirus 2 [SARS-CoV-2]) Vaccine in Adults 50 to 75 Years Old

A Phase 1 study, sponsored by ModernaTX.

Completed
Registry status
Phase 1
Development phase
392
Enrollment target

NCT05585632: Completed Phase 1 study, sponsored by ModernaTX.

NCT05585632 is a Phase 1 study that has completed, run by ModernaTX. The registered enrollment target is 392 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (553% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05585632, a Phase 1 study, has completed, sponsored by ModernaTX.

COMPLETED
Registry status
Phase 1
Development phase
392 participants
Enrollment target

Study Summary

The primary goal of this study is to evaluate the safety and reactogenicity of multi-component vaccines mRNA-1045 (Influenza and RSV) and mRNA-1230 (influenza, RSV, and SARS-CoV-2) compared with mRNA-1010 (influenza), mRNA-1345 (RSV), and mRNA-1273.214 (SARS-CoV-2) vaccines in healthy older participants.

Interventions

  • BIOLOGICAL mRNA-1345
  • BIOLOGICAL mRNA-1010
  • BIOLOGICAL mRNA-1273.214
  • BIOLOGICAL mRNA-1045
  • BIOLOGICAL mRNA-1230

Trial Details

FieldValue
Enrollment Target 392 participants
Start Date 2022-10-14
Est. Completion 2024-02-28
Phase Phase 1
ModernaTX

90 total trials

What the finished NCT05585632 record still lists

NCT05585632 is an interventional study that assigns participants to a tested intervention. The registered 392 participants enrollment target is mid-sized for trials with a published cap, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (553% higher).

The record links to 0 conditions, and to 5 interventions - of which mRNA-1345 is the first listed.

NCT05585632 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05585632 about?

NCT05585632 is a clinical study titled "A Safety, Reactogenicity, and Immunogenicity Study of mRNA-1045 (Influenza and Respiratory Syncytial Virus [RSV]) or mRNA-1230 (Influenza, RSV, and Severe Acute Respiratory Syndrome Coronavirus 2 [SARS-CoV-2]) Vaccine in Adults 50 to 75 Years Old". The primary goal of this study is to evaluate the safety and reactogenicity of multi-component vaccines mRNA-1045 (Influenza and RSV) and mRNA-1230 (influenza, RSV, and SARS-CoV-2) compared with mRNA-1010 (influenza), mRNA-1345 (RSV), and mRNA-1273.214 (SARS-CoV-2) vaccines in healthy older particip...

What is the current status of trial NCT05585632?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 392 participants. The study started on 2022-10-14. Estimated completion is 2024-02-28.

What interventions are being tested in trial NCT05585632?

The interventions under investigation include: mRNA-1345 (BIOLOGICAL), mRNA-1010 (BIOLOGICAL), mRNA-1273.214 (BIOLOGICAL), mRNA-1045 (BIOLOGICAL), mRNA-1230 (BIOLOGICAL).

Who is sponsoring clinical trial NCT05585632?

This trial is sponsored by ModernaTX, which has 90 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05585632's enrollment target sits among peer trials

392 77th of 2000 higher than 1,923 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05585632, the US trial registry maintained by the National Library of Medicine. NCT05585632 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.