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Active, not recruiting Phase 1Phase 2 Interventional Accepts healthy volunteers

Study to Evaluate the Safety, Reactogenicity, and Immunogenicity of mRNA-1403 and mRNA-1405 to Prevent Norovirus Acute Gastroenteritis in Healthy Adults 18 to 80 Years of Age

ClinicalTrials.gov ID: NCT05992935

Public ClinicalTrials.gov record NCT05992935. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 6:06 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1/2, Randomized, Placebo-Controlled, Observer-Blind, Dose-Ranging Study to Evaluate the Safety, Reactogenicity, and Immunogenicity of mRNA-1403 and mRNA-1405, Multivalent Candidate Vaccines to Prevent Norovirus Acute Gastroenteritis in Healthy Adults 18 to 80 Years of Age

Study identification

NCT ID
NCT05992935
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
ModernaTX, Inc.
Industry
Enrollment
1,407 participants

Conditions and interventions

Interventions

  • mRNA-1403 Biological
  • mRNA-1405 Biological
  • Placebo Biological

Biological

Eligibility (public fields only)

Age range
18 Years to 80 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 24, 2023
Primary completion
Sep 21, 2026
Completion
Sep 21, 2026
Last update posted
Apr 2, 2026

2023 – 2026

United States locations

U.S. sites
14
U.S. states
13
U.S. cities
14
Facility City State ZIP Site status
ARK Clinical Research, LLC Long Beach California 90815
Tekton Research, Inc - Longmont Center Longmont Colorado 80501
Research Centers of America Hollywood Florida 33024
Accel Research Sites Network Decatur Georgia 30030
Velocity Clinical Research - Boise Meridian Idaho 83642
Optimal Research Peoria Illinois 61614
Velocity Clinical Research Sioux City Iowa 51106
Johnson County Clin-Trials (JCCT) Lenexa Kansas 66219
Velocity Clinical Research Rockville Maryland 20854
Velocity Clinical Research Norfolk Nebraska 68701
Velocity Clinical Research Omaha Nebraska 68134
Rochester Clinical Research, Inc Rochester New York 14609
Epic Medical Research, LLC Red Oak Texas 75154
JBR Clinical Research Salt Lake City Utah 84107

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05992935, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 2, 2026 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05992935 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →