ClinicalTrials.gov record
Completed Phase 2 Interventional Results available

Study Evaluating the Pharmacokinetics (PK), Safety, and Tolerability of Tigecycline in Patients 8 to 11 Years of Age

ClinicalTrials.gov ID: NCT00488345

Public ClinicalTrials.gov record NCT00488345. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 17, 2026, 3:44 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Open-Label, Ascending Multiple-Dose Study to Assess the Pharmacokinetics, Safety, and Tolerability of Tigecycline in Patients 8 to 11 Years of Age With Selected Serious Infections

Study identification

NCT ID
NCT00488345
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
Industry
Enrollment
59 participants

Conditions and interventions

Eligibility (public fields only)

Age range
8 Years to 11 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 30, 2007
Primary completion
Aug 31, 2009
Completion
Aug 31, 2009
Last update posted
Oct 23, 2012

2007 – 2009

United States locations

U.S. sites
18
U.S. states
12
U.S. cities
18
Facility City State ZIP Site status
Not listed Long Beach California 90806
Not listed Oakland California 94609
Not listed Orange California 92868
Not listed San Diego California 92123
Not listed Tampa Florida 33606
Not listed Louisville Kentucky 40202
Not listed Flint Michigan 48503
Not listed Jackson Mississippi 39218
Not listed Omaha Nebraska 68131
Not listed New York New York 10032
Not listed Durham North Carolina 27710
Not listed Akron Ohio 44308
Not listed Cincinnati Ohio 45229-3039
Not listed Hershey Pennsylvania 17033-0850
Not listed Philadelphia Pennsylvania 19104
Not listed Pittsburgh Pennsylvania 15213
Not listed Salt Lake City Utah 84108
Not listed Richmond Virginia 23298

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 18 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00488345, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 23, 2012 · Synced May 17, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00488345 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →