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NCT00500266 · ClinicalTrials.gov registry record · Phase 3

Study Evaluating Safety of 13-Valent Pneumococcal Conjugate Vaccine in Healthy Elderly Subjects

A Phase 3 study, sponsored by Pfizer.

Completed
Registry status
Phase 3
Development phase
1,053
Enrollment target

NCT00500266: Completed Phase 3 study, sponsored by Pfizer.

NCT00500266 is a Phase 3 study that has completed, run by Pfizer. The registered enrollment target is 1,053 participants, above the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (36% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00500266, a Phase 3 study, has completed, sponsored by Pfizer.

COMPLETED
Registry status
Phase 3
Development phase
1,053 participants
Enrollment target

Study Summary

To evaluate the safety of 13-valent pneumococcal conjugate vaccine (13vPnC) in elderly subjects who were vaccinated with one or more doses of 23-valent pneumococcal polysaccharide vaccine (23vPS) at least 3 years before study enrollment.

Primary Outcome

Local reactions were collected by the participant using an electronic diary. Redness and swelling scaled as any(present); mild(2.5-5.0 centimeters\[cm\]); moderate(5.1-10.0 cm); severe(\>10.0cm). Pain as any(present); mild(present, no interference with activity); moderate(present, some interference with activity); severe(present, prevents daily activity). Limitation of arm movement as any(present); mild(present, could move arm above head); moderate(could move arm above shoulder but not above hea

Interventions

  • BIOLOGICAL 13-valent Pneumococcal Conjugate Vaccine (13vPnC)

Trial Details

FieldValue
Enrollment Target 1,053 participants
Start Date 2008-05
Est. Completion 2009-05
Phase Phase 3
Pfizer

1,845 total trials

What the finished NCT00500266 record still lists

NCT00500266 is an interventional study that assigns participants to a tested intervention. Its 1,053 participants enrollment target places it among the larger protocols in the corpus, above the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (36% higher).

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

NCT00500266 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00500266 about?

NCT00500266 is a clinical study titled "Study Evaluating Safety of 13-Valent Pneumococcal Conjugate Vaccine in Healthy Elderly Subjects". To evaluate the safety of 13-valent pneumococcal conjugate vaccine (13vPnC) in elderly subjects who were vaccinated with one or more doses of 23-valent pneumococcal polysaccharide vaccine (23vPS) at least 3 years before study enrollment.

What is the current status of trial NCT00500266?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 1,053 participants. The study started on 2008-05. Estimated completion is 2009-05.

What interventions are being tested in trial NCT00500266?

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

Who is sponsoring clinical trial NCT00500266?

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

How this trial's enrollment target compares

Where NCT00500266's enrollment target sits among peer trials

1,053 278th of 2000 higher than 1,723 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00500266, the US trial registry maintained by the National Library of Medicine. NCT00500266 (large enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.