CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 792 enrolled
Drug / intervention
Live, attenuated dengue serotype 1, 2, 3, and 4 virus +12 morebiological
Likely dose
Live, attenuated dengue serotype 1, 2, 3, and 4 virus 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/NCT01436396
NCT01436396Phase 3Completed

Immunogenicity and Safety of Yellow Fever Vaccine (Stamaril®) Administered Concomitantly With Tetravalent Dengue Vaccine in Healthy Toddlers at 12-13 Months of Age in Colombia and Peru

Sanofi Pasteur, a Sanofi Company·interventional·Posted Sep 19, 2011·Updated Mar 25, 2022

In Brief

A Phase 3 clinical trial evaluating Live, attenuated dengue serotype 1, 2, 3, and 4 virus, Yellow fever vaccine, and 7 other interventions for Dengue and 2 related conditions. Completed, enrolled 792 participants across 2 sites in 2 countries.

Detailed Summary

The study was designed to evaluate whether the first CYD dengue vaccination can be administered concomitantly with Stamaril® yellow fever vaccine during the same day and visit, but at 2 different sites of administration. Primary Objective: * To demonstrate the non-inferiority of the immune response against Yellow Fever (YF) in flavivirus (FV) non-immune subjects at baseline receiving one dose of Stamaril vaccine administered concomitantly with the first dose of CYD dengue vaccine compared to participants receiving one dose of Stamaril vaccine concomitantly with placebo. Secondary Objectives: * To assess the non-inferiority of YF immune response 28 days post-Stamaril vaccination based on seroconversion rates regardless of the FV status of participants at baseline. * To describe the YF immune response 28 days post-Stamaril vaccination in both groups. * To describe the antibody (Ab) response to each dengue virus serotype 28 days post CYD dengue vaccine (Visit \[V\] 05 and V07), following CYD dengue vaccine Dose 1 and Dose 2 from Group 2 versus following CYD dengue vaccine Dose 2 and Dose 3 for Group 1 (effect of YF vaccination). * To describe the safety of Stamaril vaccine administered concomitantly with the first dose of CYD dengue vaccine, or Stamaril administered concomitantly with placebo. * To describe the safety of CYD dengue vaccine after the first dose of CYD dengue vaccine administered concomitantly with Stamaril vaccine or CYD vaccine administered alone. * To describe the safety of the CYD dengue vaccine in all participants after each dose.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesColombia, Peru
Collaborators--

Timeline

Phase 3CompletedFinished
201220132014201520162017201820192020202120222023202420252026
First PostedSep 19, 2011
Enrollment StartSep 7, 2011
Primary CompletionSep 1, 2013
Study CompletionSep 2, 2013
TodayJul 2, 2026
Enrollment to primary: 2.0 yearsPosted 14.8 years ago

Interventions

Live, attenuated dengue serotype 1, 2, 3, and 4 virusbiological

0.5 mL, subcutaneous at age 12, 18, and 24 months

Yellow fever vaccinebiological

0.5 mL subcutaneous in the deltoid at age 12 to 13 months.

Measles, mumps, and rubella (MMR) vaccinebiological

0.5 mL, subcutaneous at age 12 to 13 months.

Pneumococcal Conjugated Vaccinebiological

0.5 mL, intramuscular at age 13 to 14 months

Hepatitis A Pediatric Vaccinebiological

0.5 mL, intramuscular at age 13 to 14 months and 25 to 26 months

Diphtheria, tetanus, pertussis, polio, and Haemophilus influenzae vaccinebiological

0.5 mL, intramuscular at age 19 to 20 months

Live, attenuated dengue serotype 1, 2, 3, and 4 virusbiological

0.5 mL, subcutaneous at age 18 to 19 and 24 to 25 months

Yellow Fever Vaccinebiological

0.5 mL, subcutaneous at age 12 to 13 months

Placebo (NaCl)biological

0.5 mL, subcutaneous at age 12 to 13 months

Measles, mumps, and rubella vaccinebiological

0.5 mL, subcutaneous at age 13 to 14 months

Pneumococcal Conjugated Vaccinebiological

0.5 mL, intramuscular at age 13 to 14 months

Diphtheria, tetanus, pertussis, polio, and Haemophilus influenzae vaccinebiological

0.5 mL, intramuscular at age 19 to 20 months

Hepatitis A Pediatric Vaccinebiological

0.5 mL, intramuscular at age 13 to 14 months and 25 to 26 months