Blood Collection In Healthy Adult Volunteers To Obtain Serum For Use In Serum Bactericidal Activity Assay Development

NCT ID: NCT00401232

Last Updated: 2018-03-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

955 participants

Study Classification

INTERVENTIONAL

Study Start Date

2006-08-31

Study Completion Date

2017-12-31

Brief Summary

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This is a study to collect blood from volunteers to assist in assay development.

Detailed Description

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Conditions

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Healthy Subjects

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Study Groups

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Arm 1

Group Type OTHER

Blood Collection

Intervention Type PROCEDURE

Blood Collection

Interventions

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Blood Collection

Blood Collection

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Healthy Volunteers aged 18-64

Exclusion Criteria

* Bleeding disorder
Minimum Eligible Age

18 Years

Maximum Eligible Age

64 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Pfizer

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Pfizer CT.gov Call Center

Role: STUDY_DIRECTOR

Pfizer

Locations

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SNBL Clinical Pharmacology Center

Baltimore, Maryland, United States

Site Status

Frontage Clinical Services Inc

Hackensack, New Jersey, United States

Site Status

Countries

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United States

Related Links

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Other Identifiers

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B1971032

Identifier Type: OTHER

Identifier Source: secondary_id

6108A1-800

Identifier Type: -

Identifier Source: org_study_id

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