Trials Sponsors Conditions Drugs Pricing

Conditions

Pandemic Influenza

Keywords

Pandemic influenzaVaccine

Outcome Measures

Primary Outcomes (1)

To identify the preferred vaccine formulation dosage (antigen & adjuvant) and schedule (one or two administrations) of the H1N1sw monovalent vaccine in children and adolescents
43 days after first vaccination

Secondary Outcomes (1)

To evaluate immunogenicity against A/California H1N1sw strain after booster dose of egg-derived seasonal trivalent, MF59 adjuvanted vaccine Fluad, recommended for 2010/2011 season, administered 12 months after primary course according to CHMP criteria.
3 weeks after booster vaccination

Study Arms (3)

low dose of antigen + low dose of adjuvant

EXPERIMENTAL

Biological: Monovalent A/H1N1 influenza vaccine

high dose of antigen + high dose of adjuvant

EXPERIMENTAL

Biological: Monovalent A/H1N1 influenza vaccine

high dose of antigen

EXPERIMENTAL

Biological: Monovalent A/H1N1 influenza vaccine

Interventions

Monovalent A/H1N1 influenza vaccineBiological

This trial will be performed at multiple study sites in a population of healthy children and adolescent. Subjects will be randomized to receive 2 IM injections of low dose of antigen \& adjuvant, or high dose of antigen \& adjuvant, or high dose of antigen, according to the study groups.

high dose of antigenhigh dose of antigen + high dose of adjuvantlow dose of antigen + low dose of adjuvant

Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.

Eligibility Criteria

Age6 Months - 17 Years

Sexall

Healthy VolunteersYes

Age GroupsChild (0-17)

You may qualify if:

Males and females 6 months of age to 17 years of age on the day of enrollment;
Subject's parents or legal guardians who have given written consent and the subjects has given assent consent, if applicable;

Sponsors & Collaborators

Novartis Vaccines
Industrylead

Study Sites (5)

Gent, Antwerpen, Belgium

Santigo de chile

Santiago, Chile

Gazcue Santo Domingo

Gazcue Santo Domingo, Dominican Republic

Wurzburg, Fulda, Neumunster, Balve, Stuttgart-Feuerbach, Leipzig, Rostock, Mainz, Detmold, Alsfeld

Mainz, Germany

Rotterdam, Netherlands

Related Publications (1)

Knuf M, Leroux-Roels G, Rumke HC, Abarca K, Rivera L, Lattanzi M, Pedotti P, Arora A, Kieninger-Baum D, Della Cioppa G. Safety and immunogenicity of an MF59-adjuvanted A/H1N1 pandemic influenza vaccine in children from three to seventeen years of age. Vaccine. 2015 Jan 1;33(1):174-81. doi: 10.1016/j.vaccine.2014.10.085. Epub 2014 Nov 11.
PMID: 25444803DERIVED

Enrollment

778 participants (actual enrollment reported by the registry).

Study Design

Study Type: interventional
Phase: phase 3
Allocation: RANDOMIZED
Masking: SINGLE
Who Masked: INVESTIGATOR
Purpose: PREVENTION
Intervention Model: PARALLEL
Sponsor Type: INDUSTRY
Responsible Party: SPONSOR

Study Record Dates

First Submitted

September 2, 2009

First Posted

September 3, 2009

Study Start

September 2009

Date type not reported

This date has not been verified as actual or estimated.

You may not qualify if:

Subject's parents or legal guardians who are not able to comprehend and to follow all required study procedures;
Individuals with history or any illness that, in the opinion of the investigator, might interfere with the results of the study or pose additional risk to the subjects due to participation in the study;
Individuals with any serious chronic or progressive disease according to judgment of the investigator;
History of any anaphylaxis, serious vaccine reactions to any excipients and to eggs (including ovalbumin) and chicken protein;
Individuals who have had adjuvanted influenza vaccine or documented confirmed or suspected influenza disease within 3 months prior to Day 1.
Receipt of another investigational agent within 4 weeks prior to enrollment or before completion of the safety follow-up period in this or in another study, unwilling to refuse a participation in another clinical study through the end of this study;
Individuals who receive any other vaccine 4 weeks prior to enrolment in this study or who are planning to receive any vaccine within four weeks from the study vaccines; the only exception being plain seasonal influenza vaccines which are allowed until one week prior to and after one week study vaccinations;
Individuals who have received blood, blood products and/or plasma derivatives or any parenteral immunoglobulin preparation in the past 12 weeks;
Individuals with axillary temperature ≥ 38.0 degrees Celsius within 3 days of intended study vaccination;
Known or suspected alteration of immune function;
History of progressive or severe neurologic disorder;
Surgery planned during the study period that in the Investigator's opinion would interfere with the study visits schedule;
If female, of childbearing potential, and has not used any of the "acceptable contraceptive methods" for at least 2 months prior to study entry;
Females who are pregnant or nursing (breastfeeding) mothers, or females of childbearing potential do not plan to use acceptable birth control measures during the first 3 weeks after vaccination;
Members of research staff or their relatives.

Immunogenicity, Safety and Tolerability of Two Doses of Adjuvanted and Non-adjuvanted Swine Origin A/H1N1 Monovalent Influenza Vaccine (Egg-Derived) in Healthy Subjects From 6 Months to 17 Years of Age

Brief Summary

Registry Overview

Trial Relationships

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Secondary Outcomes (1)

Study Arms (3)

low dose of antigen + low dose of adjuvant

high dose of antigen + high dose of adjuvant

high dose of antigen

Interventions

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (5)

Related Publications (1)

Enrollment

Study Design

Study Record Dates

You may not qualify if:

Source record

Locations

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Secondary Outcomes (1)

Study Arms (3)

low dose of antigen + low dose of adjuvant

high dose of antigen + high dose of adjuvant

high dose of antigen

Interventions

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (5)

Related Publications (1)

Enrollment

Study Design

Study Record Dates

You may not qualify if:

Source record

Locations