Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 1 Interventional Accepts healthy volunteers Results available

Safety and Immunogenicity of Three Dosage Levels of Swine Influenza Vaccine in Children Ages 3 to <9 Years, Adolescents 9 to <18 Years, Adults 18 to <65 Years and Elderly 65 Years and Older.

ClinicalTrials.gov ID: NCT01855945

Public ClinicalTrials.gov record NCT01855945. 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, 4:46 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

Phase I Multi-center, Observer-Blind, Randomized, Dose-Ranging Study of Adjuvanted and Non-Adjuvanted Cell Culture-Derived, Inactivated Novel Swine Origin A/H3N2v Monovalent Subunit Influenza Virus Vaccine (H3N2c) in Children Ages 3 to <9 Years, Adolescents 9 to <18 Years, Adults 18 to < 65 Years and Elderly ≥ 65 Years and Older.

Study identification

NCT ID
NCT01855945
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Novartis Vaccines
Industry
Enrollment
627 participants

Conditions and interventions

Interventions

  • Swine Influenza Biological

Biological

Eligibility (public fields only)

Age range
3 Years to 92 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
Apr 30, 2013
Primary completion
Aug 31, 2014
Completion
Aug 31, 2014
Last update posted
Feb 16, 2016

2013 – 2014

United States locations

U.S. sites
11
U.S. states
9
U.S. cities
11
Facility City State ZIP Site status
51, Northern California Clinical Research Center Redding California 96001
47, Benchmark Research Sacramento California 95822
46, Johnson County Clinical Trials Lenexa Kansas 66213
49, Heartland Research Associates, LLC Wichita Kansas 67207
43, Central Kentucky Research Associates Lexington Kentucky 40509
41, Benchmark Research Metairie Louisiana 70006
44, Rochester Clinical Research Inc. Rochester New York 14609
50, PMG Research of Raleigh Raleight North Carolina 27609
45, Omega Medical Research Warwick Rhode Island 02886
42, Research Acros Dallas Texas 75234
48, "J. Lewis Research, Inc. Salt Lake City Utah 84109

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 NCT01855945, 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 Feb 16, 2016 · Synced Jul 21, 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 NCT01855945 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →