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Completed Phase 3 Interventional

Treatment of Neutropenic Patients With Fever Who Are Suspected to Have A Gram Positive Infection

ClinicalTrials.gov ID: NCT00035425

Public ClinicalTrials.gov record NCT00035425. 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 Oct 21, 2026, 1:10 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 Randomized, Double-Blind Trial Comparing Linezolid To Vancomycin In The Empiric Treatment Of Febrile Neutropenic Oncology Patients With Suspected Gram-Positive Infections

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study will treat patients who have fever and neutropenia (after cancer chemotherapy) that is possibly due to a specific bacteria (gram positive bacteria).

Study identification

NCT ID
NCT00035425
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pfizer
Industry
Enrollment
120 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
13 Years and older
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 2001 (Type not available)
Primary completion
Not listed
Completion
Nov 2002 (Actual)
Last update posted
Dec 1, 2009

2001 – 2002

United States locations

U.S. sites
16
U.S. states
6
U.S. cities
8
Facility City State ZIP Site status
Pfizer Investigational Site Los Angeles California 90033 —
Pfizer Investigational Site Springfield Illinois 62701-1014 —
Pfizer Investigational Site Springfield Illinois 62703 —
Pfizer Investigational Site Springfield Illinois 62769 —
Pfizer Investigational Site Springfield Illinois 62781 —
Pfizer Investigational Site The Bronx New York 10461 —
Pfizer Investigational Site The Bronx New York 10467 —
Pfizer Investigational Site Houston Texas 77030 —
Pfizer Investigational Site Richmond Virginia 23226 —
Pfizer Investigational Site Richmond Virginia 23229 —
Pfizer Investigational Site Richmond Virginia 23249 —
Pfizer Investigational Site Richmond Virginia 23294-4367 —
Pfizer Investigational Site Richmond Virginia 23294 —
Pfizer Investigational Site Federal Way Washington 98003 —
Pfizer Investigational Site Lakewood Washington 98499 —
Pfizer Investigational Site Tacoma Washington 98405 —

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 24 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00035425, 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 Dec 1, 2009 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00035425 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →