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Completed Phase 1 Interventional Accepts healthy volunteers

Safety and Immunogenicity Study of Self-Amplifying RNA Pandemic Influenza Vaccine in Adults

ClinicalTrials.gov ID: NCT06602531

Public ClinicalTrials.gov record NCT06602531. 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 23, 2026, 5:48 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, First-in-human, Randomized, Observer-blind, Parallel Design, Controlled, Dose Level and Schedule-finding Study to Evaluate the Safety, Reactogenicity, and Immunogenicity of a Self-Amplifying mRNA Pandemic Influenza Vaccine (ARCT-2304) When Administered to Healthy Adults

Study identification

NCT ID
NCT06602531
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Arcturus Therapeutics, Inc.
Industry
Enrollment
212 participants

Conditions and interventions

Interventions

  • ARCT-2304 Biological
  • Control vaccine (licensed seasonal influenza vaccine) younger adults Biological
  • Control vaccine (licensed seasonal influenza vaccine) older adults Biological
  • Placebo Vaccine Other

Biological · Other

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
Dec 9, 2024
Primary completion
Jun 12, 2025
Completion
Dec 4, 2025
Last update posted
Apr 2, 2026

2024 – 2025

United States locations

U.S. sites
4
U.S. states
3
U.S. cities
4
Facility City State ZIP Site status
Velocity Clinical Research La Mesa California 91942
Velocity Clinical Research San Bernardino California 92408
Tekton Research Longmont Colorado 80501
CTI Clinical Research Center Cincinnati Ohio 45212

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06602531, 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 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06602531 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →