CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 849 enrolled
Drug / intervention
Monovalent Subvirion A/H1N1 Influenza vaccine (7.5 µg of HA) +3 morebiological
Likely dose
Monovalent Subvirion A/H1N1 Influenza vaccine (7.5 µg of HA)from record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00953524
NCT00953524Phase 2Completed

Immunogenicity and Safety of Multiple Formulations of an A/H1N1 Pandemic Vaccine in Healthy Adult and Elderly Subjects

Sanofi Pasteur, a Sanofi Company·interventional·Posted Aug 6, 2009·Updated Mar 10, 2014

In Brief

A Phase 2 clinical trial evaluating Monovalent Subvirion A/H1N1 Influenza vaccine (7.5 µg of HA), Monovalent Subvirion A/H1N1 Influenza vaccine (15 µg of HA), and 2 other interventions for Influenza and Swine-origin A/H1N1 Influenza. Completed, enrolled 849 participants across 15 sites.

Detailed Summary

The purpose of the study is to evaluate different doses of the Influenza A/H1N1 pandemic vaccine. Primary Objectives: * To describe the immunogenicity of the candidate vaccines after each injection. * To describe the safety of the candidate vaccines after each injection.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedAug 6, 2009
Enrollment StartAug 1, 2009
Primary CompletionMar 1, 2010
Study CompletionDec 1, 2010
TodayJul 2, 2026
Enrollment to primary: 7 monthsPosted 16.9 years ago

Interventions

Monovalent Subvirion A/H1N1 Influenza vaccine (7.5 µg of HA)biological

0.5 mL, Intramuscular on Day 0 and on Day 21

Monovalent Subvirion A/H1N1 Influenza vaccine (15 µg of HA)biological

0.5 mL, Intramuscular on Day 0 and Day 21

Monovalent Subvirion A/H1N1 Influenza vaccine (30 µg of HA)biological

0.5 mL, Intramuscular on Day 0 and day 21

Normal saline solution (placebo)biological

0.5 mL, Intramuscular on Day 0 and Day 21