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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Study of the Effect of Pneumococcal Conjugate Vaccine (PCV) on Immunogenicity of Pentacel™

ClinicalTrials.gov ID: NCT00772928

Public ClinicalTrials.gov record NCT00772928. 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 Sep 2, 2026, 6:44 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Immunogenicity Assessment of Pentacel™ (Hybrid CP20/20/5/3DT-mIPV//PRP-T) When Given at Different Times From or Concurrently With a Pneumococcal Conjugate Vaccine

Brief summary

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

This study is designed to evaluate in a controlled manner the effect of Prevnar® on the immune responses of Pentacel™ Primary Objective - Stage I: To compare the immune responses elicited by an infant series of Pentacel™ when given at different times from or concurrently with a Pneumococcal conjugate vaccine (Prevnar®). Primary Objective - Stage II: To compare the immune responses elicited by a 4th dose of Pentacel™ when given at different times from or concurrently with Prevnar®.

Study identification

NCT ID
NCT00772928
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Sanofi
Industry
Enrollment
1,167 participants

Conditions and interventions

Eligibility (public fields only)

Age range
42 Days to 89 Days
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
Sep 30, 2003
Primary completion
Apr 30, 2006
Completion
Oct 31, 2006
Last update posted
Jan 31, 2012

2003 – 2006

United States locations

U.S. sites
23
U.S. states
13
U.S. cities
22
Facility City State ZIP Site status
Not listed Montgomery Alabama 36106
Not listed Fayetteville Arkansas 72703
Not listed Jonesboro Arkansas 72401
Not listed Little Rock Arkansas 72205
Not listed Fountain Valley California 92708
Not listed Oakland California 94612
Not listed Rolling Hills Estate California 90274
Not listed Norwich Connecticut 06360
Not listed Bardstown Kentucky 40004
Not listed Louisville Kentucky 40202
Not listed Boston Massachusetts 02115
Not listed Kansas City Missouri 64112
Not listed Brooklyn New York 11201
Not listed Norristown Pennsylvania 19401
Not listed Pittsburgh Pennsylvania 15241
Not listed Austin Texas 78745
Not listed Fort Worth Texas 76107
Not listed San Antonio Texas 78229
Not listed San Antonio Texas 78745
Not listed Layton Utah 84041
Not listed Spokane Washington 99220
Not listed Vancouver Washington 98864
Not listed La Crosse Wisconsin 54601

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 NCT00772928, 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 Jan 31, 2012 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00772928 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →