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NCT00824850 · ClinicalTrials.gov registry record · Phase 2

Study Evaluating Prevnar Infant Long-term Immune Response Versus Prevnar Naive Cohort

A Phase 2 study, sponsored by Pfizer.

Completed
Registry status
Phase 2
Development phase
75
Enrollment target

NCT00824850 is a Phase 2 study that has completed, run by Pfizer. The registered enrollment target is 75 participants.

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The verdict

NCT00824850, a Phase 2 study, has completed, sponsored by Pfizer.

COMPLETED
Registry status
Phase 2
Development phase
75 participants
Enrollment target

Study Summary

The purpose of this study is to assess the "late" immune response to further doses of pneumococcal conjugate vaccine more than 10 years after primary immunization with Prevnar (7vPnC) in infancy, as compared with individuals who did not receive Prevnar in infancy (the Prevnar naive cohort which received MnCC). The study will take place at a single study center. Study participants must have participated previously in a specific Wyeth Prevnar study (Study D118-P8) and must still be enrolled in the Northern California Kaiser Permanente (NCKP) health plan.

Interventions

  • BIOLOGICAL 13-valent Pneumococcal Conjugate Vaccine

Trial Details

FieldValue
Enrollment Target 75 participants
Start Date 2010-01
Est. Completion 2010-09
Phase Phase 2

Sponsor

Pfizer

1,845 total trials

What the Registry Record Tells You About NCT00824850

The ClinicalTrials.gov registry entry for NCT00824850 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 75 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pfizer, which has 1,845 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which 13-valent Pneumococcal Conjugate Vaccine is the first listed.

NCT00824850 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00824850 about?

NCT00824850 is a clinical study titled "Study Evaluating Prevnar Infant Long-term Immune Response Versus Prevnar Naive Cohort". The purpose of this study is to assess the "late" immune response to further doses of pneumococcal conjugate vaccine more than 10 years after primary immunization with Prevnar (7vPnC) in infancy, as compared with individuals who did not receive Prevnar in infancy (the Prevnar naive cohort which rece...

What is the current status of trial NCT00824850?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 75 participants. The study started on 2010-01. Estimated completion is 2010-09.

What interventions are being tested in trial NCT00824850?

The interventions under investigation include: 13-valent Pneumococcal Conjugate Vaccine (BIOLOGICAL).

Who is sponsoring clinical trial NCT00824850?

This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.