CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 116 enrolled
Drug / intervention
Menactra®: Meningococcal Polysaccharide Diphtheria Toxoid Conjugatebiological
Likely dose
Menactra®: Meningococcal Polysaccharide Diphtheria Toxoid Conjugate 0.5 mLfrom 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/NCT01689155
NCT01689155N/ACompleted

Post-licensure Safety Surveillance Study of Menactra® Vaccine When Administered As a 2-dose Schedule to Children 9 Months Through 23 Months of Age.

Sanofi Pasteur, a Sanofi Company·observational·Posted Sep 21, 2012·Updated Nov 11, 2016

In Brief

An observational study evaluating Menactra®: Meningococcal Polysaccharide Diphtheria Toxoid Conjugate for Meningitis and Meningococcal Infection. Completed, enrolled 116 participants across 1 site.

Detailed Summary

This is a passive-surveillance study that will accrue subjects for surveillance. For each accrued subject, surveillance for outcomes will continue for six months following the first dose. If a second dose is given within that time, then surveillance will be continued for six months following the second dose. Observational Objective: * To describe and characterize adverse events occurring after vaccination with Menactra vaccine.

Study Details

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

Timeline

N/ACompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
First PostedSep 21, 2012
Enrollment StartJun 1, 2011
Primary CompletionJun 1, 2015
Study CompletionApr 1, 2016
TodayJul 2, 2026
Enrollment to primary: 4 yearsPosted 13.8 years ago

Interventions

Menactra®: Meningococcal Polysaccharide Diphtheria Toxoid Conjugatebiological

0.5 mL, Intramuscular