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COMPLETED Phase 3

Study Comparing 13-valent Pneumococcal Conjugate Vaccine With 7-valent Pneumococcal Conjugate Vaccine

NCT00373958 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to evaluate the safety, tolerability, and immunogenicity of the 13-valent pneumococcal vaccine (13vPnC) compare to the 7-valent pneumococcal vaccine (7vPnC) and to compare the immune response to concomitant vaccines administered with 13vPnC and 7vPnC.

Conditions Studied

Interventions

  • BIOLOGICAL 13 valent pneumococcal conjugate vaccine
  • BIOLOGICAL 7vPnc pneumococcal conjugate vaccine

Study Locations (20)

California

  • — Downey
  • — Fontana
  • — Loma Linda
  • — Paramount
  • — Riverside

Arkansas

  • — Fayetteville
  • — Jonesboro
  • — Little Rock

Kentucky

  • — Bardstown
  • — Louisville
  • — Louisville

Georgia

  • — Marietta
  • — Woodstock

Illinois

  • — Chicago
  • — Park Ridge

Colorado

  • — Centennial

Connecticut

  • — Norwich

Florida

  • — Tampa

Trial Details

FieldValue
Enrollment Target 666 participants
Start Date 2006-09
Est. Completion 2008-06
Phase Phase 3

Sponsor

Pfizer

769 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00373958

The ClinicalTrials.gov registry entry for NCT00373958 describes a study currently listed as completed. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 666 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pfizer, which has 769 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Vaccines, Pneumococcal appearing as the primary indexed condition, and to 2 interventions — of which 13 valent pneumococcal conjugate vaccine is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00373958 reports 20 study locations spanning 10 distinct geographic areas — top geographies include California, Arkansas, Kentucky. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00373958 about?

NCT00373958 is a clinical study titled "Study Comparing 13-valent Pneumococcal Conjugate Vaccine With 7-valent Pneumococcal Conjugate Vaccine". The purpose of this study is to evaluate the safety, tolerability, and immunogenicity of the 13-valent pneumococcal vaccine (13vPnC) compare to the 7-valent pneumococcal vaccine (7vPnC) and to compare the immune response to concomitant vaccines administered with 13vPnC and 7vPnC.

What is the current status of trial NCT00373958?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 666 participants. The study started on 2006-09. Estimated completion is 2008-06.

What conditions does trial NCT00373958 study?

This clinical trial studies the following conditions: Vaccines, Pneumococcal. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00373958?

The interventions under investigation include: 13 valent pneumococcal conjugate vaccine (BIOLOGICAL), 7vPnc pneumococcal conjugate vaccine (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00373958?

This trial is sponsored by Pfizer, which has 769 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00373958 being conducted?

This trial has 20 study locations across Arkansas, California, Colorado, Connecticut, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial