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Completed Phase 4 Interventional Accepts healthy volunteers Results available

Safety and Immunogenicity of Sequential Rotavirus Vaccine Schedules

ClinicalTrials.gov ID: NCT01266850

Public ClinicalTrials.gov record NCT01266850. 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 Oct 17, 2026, 5:18 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

Safety and Immunogenicity of Sequential Rotavirus Vaccine Schedules With RotaTeq® and Rotarix®

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Rotavirus, sometimes called the "stomach flu," is the most common cause of severe diarrhea in children. Vaccines can prevent many types of infections and work by causing the body to make proteins called antibodies that fight infection. For some vaccines, more than one vaccination is needed so that the body will make enough antibodies to fight infection. The vaccines (RotaTeq® or Rotarix® oral vaccines) given in this study are recommended for infants by the Centers for Disease Control and Prevention (CDC) Advisory Committee on Immunization Practices (ACIP). These vaccines require either 2 or 3 vaccinations to be effective. Healthy infants between 6 weeks and 14 weeks, 6 days of age at Visit 1 will participate for about 10-12 months. Study procedures include reaction assessment and blood sample.

Study identification

NCT ID
NCT01266850
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Enrollment
1,384 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
6 Weeks to 14 Weeks
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
Mar 2011 (Type not available)
Primary completion
Oct 2013 (Actual)
Completion
Mar 2014 (Actual)
Last update posted
Oct 28, 2014

2011 – 2014

United States locations

U.S. sites
13
U.S. states
10
U.S. cities
11
Facility City State ZIP Site status
Kaiser Permanente Vaccine Study Center Oakland California 94612-3610 —
Children's Hospital & Research Center Oakland - Primary Care Clinic Oakland California 94618-1033 —
Emory Children's Center - Pediatric Infectious Diseases Atlanta Georgia 30322-1014 —
University of Iowa - Vaccine Research & Education Unit Iowa City Iowa 52242-2600 —
University of Maryland School of Medicine - Center for Vaccine Development - Baltimore Baltimore Maryland 21201-1509 —
Children's Mercy Hospital and Clinics - Infectious Diseases Kansas City Missouri 64108-4619 —
Duke Translational Medicine Institute - Clinical Vaccine Unit Durham North Carolina 27704-2120 —
Primary Physicians Research Inc. - Pittsburgh Pittsburgh Pennsylvania 15241-3100 —
Vanderbilt University - Pediatric - Vanderbilt Vaccine Research Center Nashville Tennessee 37232-2573 —
The University of Texas Medical Branch - Sealy Center for Vaccine Development (SCVD) Galveston Texas 77555-1121 —
Baylor College of Medicine - Molecular Virology and Microbiology Houston Texas 77030-3411 —
Group Health Research Institute - Seattle Seattle Washington 98101-1466 —
Seattle Children's Hospital - Infectious Diseases Seattle Washington 98105-3901 —

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 NCT01266850, 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 Oct 28, 2014 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01266850 live on ClinicalTrials.gov.

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