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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Efficacy, Safety, and Immunogenicity of a Plant-Derived Quadrivalent Virus-Like Particles (VLPs) Influenza Vaccine in Adults

ClinicalTrials.gov ID: NCT03301051

Public ClinicalTrials.gov record NCT03301051. 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 Sep 5, 2026, 6:13 AM 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 Randomized, Observer-blind, Placebo-controlled, Multicenter, Phase 3 Study to Assess the Efficacy, Safety, and Immunogenicity of a Plant-Derived Quadrivalent Virus-Like Particles Influenza Vaccine in Adults 18-64 Years of Age

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This Phase 3 study is intended to assess the efficacy of the Quadrivalent VLP Influenza Vaccine during the 2017-2018 influenza season in healthy adults 18 to 64 years of age. One dose of Quadrivalent VLP Influenza Vaccine (30 μg/strain) or of placebo will be administered to approximately 10,000 participants

Study identification

NCT ID
NCT03301051
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Medicago
Industry
Enrollment
10,160 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 64 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 30, 2017
Primary completion
May 1, 2018
Completion
May 8, 2018
Last update posted
Aug 13, 2023

2017 – 2018

United States locations

U.S. sites
29
U.S. states
18
U.S. cities
26
Facility City State ZIP Site status
Site 222 Mobile Alabama 36608
Site 210 Anaheim California 92801
Site 223 Milford Connecticut 06460
Site 217 Coral Gables Florida 33134
Site 220 Hollywood Florida 33024
Site 212 South Miami Florida 33143
Site 203 Savannah Georgia 31406
Site 218 Stockbridge Georgia 30281
Site 206 Wichita Kansas 67025
Site 202 Metairie Louisiana 70006
Site 225 St Louis Missouri 63141
Site 224 Norfolk Nebraska 68701
Site 208 Omaha Nebraska 63134
Site 213 Las Vegas Nevada 89104
Site 205 Binghamton New York 13901
Site 228 Endwell New York 13760
Site 216 Charlotte North Carolina 28209
Site 221 Charlotte North Carolina 28277
Site 227 Winston-Salem North Carolina 27103
Site 201 Columbus Ohio 43123
Site 207 Dakota Dunes South Dakota 57049
Site 209 Bristol Tennessee 37260
Site 204 Austin Texas 78705
Site 229 Austin Texas 78745
Site 226 Fort Worth Texas 76104
Site 219 Fort Worth Texas 76135
Site 214 Salt Lake City Utah 84124
Site 211 West Jordan Utah 84088
Site 230 Norfolk Virginia 23507

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 44 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03301051, 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 Aug 13, 2023 · Synced Sep 5, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03301051 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →