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NCT02124161 · ClinicalTrials.gov registry record · Phase 4

Concomitant Administration of 13-valent Pneumococcal Conjugate Vaccine (13vPnC) With Influenza Vaccine in 23-valent Pneumococcal Polysaccharide (23vPS) Pre-vaccinated Adults.

A Phase 4 study, sponsored by Pfizer.

Completed
Registry status
Phase 4
Development phase
882
Enrollment target

NCT02124161 is a Phase 4 study that has completed, run by Pfizer. The registered enrollment target is 882 participants.

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The verdict

NCT02124161, a Phase 4 study, has completed, sponsored by Pfizer.

COMPLETED
Registry status
Phase 4
Development phase
882 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the immunogenicity and safety of 13-valent pneumococcal polysaccharide vaccine when given concomitantly with seasonal inactivated influenza vaccine to adults 50 years and older who have previously received 23-valent pneumococcal polysaccharide vaccine.

Interventions

  • OTHER Placebo
  • BIOLOGICAL Seasonal Inactivated Influenza Vaccine
  • BIOLOGICAL 13-valent pneumococcal conjugate vaccine

Trial Details

FieldValue
Enrollment Target 882 participants
Start Date 2014-09
Est. Completion 2015-05
Phase Phase 4

Sponsor

Pfizer

1,845 total trials

What the Registry Record Tells You About NCT02124161

The ClinicalTrials.gov registry entry for NCT02124161 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 882 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 3 interventions - of which Placebo is the first listed.

NCT02124161 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02124161 about?

NCT02124161 is a clinical study titled "Concomitant Administration of 13-valent Pneumococcal Conjugate Vaccine (13vPnC) With Influenza Vaccine in 23-valent Pneumococcal Polysaccharide (23vPS) Pre-vaccinated Adults.". The purpose of this study is to evaluate the immunogenicity and safety of 13-valent pneumococcal polysaccharide vaccine when given concomitantly with seasonal inactivated influenza vaccine to adults 50 years and older who have previously received 23-valent pneumococcal polysaccharide vaccine.

What is the current status of trial NCT02124161?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 882 participants. The study started on 2014-09. Estimated completion is 2015-05.

What interventions are being tested in trial NCT02124161?

The interventions under investigation include: Placebo (OTHER), Seasonal Inactivated Influenza Vaccine (BIOLOGICAL), 13-valent pneumococcal conjugate vaccine (BIOLOGICAL).

Who is sponsoring clinical trial NCT02124161?

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.