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Completed Phase 3 Interventional Results available

Safety & Immunogenicity of 13vPnC in HIV-Infected Subjects Aged 18 or Older Who Were Previously Immunized With 23vPS

ClinicalTrials.gov ID: NCT00963235

Public ClinicalTrials.gov record NCT00963235. 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 19, 2026, 3:16 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

A Phase 3, Open-label, Single-Arm Trial to Evaluate the Safety, Tolerability, and Immunogenicity of 3 Doses of 13vPnC Vaccine in HIV-Infected Subjects 18 Years of Age or Older Who Have Been Previously Immunized With 23vPS Vaccine

Brief summary

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

The study will evaluate the safety, tolerability and immunogenicity of a 13-valent pneumococcal conjugate vaccine (13vPnC) in HIV-infected subjects 18 years of age or older who have been previously immunized with at least one dose of 23-valent pneumococcal polysaccharide vaccine (23vPS). All subjects will receive 3 doses of 13vPnC, with each study vaccine dose given approximately 6 months apart.

Study identification

NCT ID
NCT00963235
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pfizer
Industry
Enrollment
331 participants

Conditions and interventions

Interventions

Biological · Procedure

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 2009 (Type not available)
Primary completion
May 2012 (Actual)
Completion
May 2012 (Actual)
Last update posted
Jun 10, 2013

2009 – 2012

United States locations

U.S. sites
15
U.S. states
9
U.S. cities
11
Facility City State ZIP Site status
Pfizer Investigational Site San Francisco California 94115 —
Pfizer Investigational Site Aurora Colorado 80045 —
Pfizer Investigational Site Washington D.C. District of Columbia 20009 —
Pfizer Investigational Site Lexington Kentucky 40536 —
Pfizer Investigational Site Springfield Massachusetts 01199 —
Pfizer Investigational Site St Louis Missouri 63110 —
Pfizer Investigational Site New York New York 10011 —
Pfizer Investigational Site New York New York 10016 —
Pfizer Investigational Site New York New York 10029 —
Pfizer Investigational Site New York New York 10032 —
Pfizer Investigational Site New York New York 10065 —
Pfizer Investigational Site Rochester New York 14642 —
Pfizer Investigational Site Johnson City Tennessee 37604 —
Pfizer Investigational Site Austin Texas 78705 —
Pfizer Investigational Site Dallas Texas 75246 —

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 NCT00963235, 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 Jun 10, 2013 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00963235 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →