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Completed Phase 2 Interventional

Safety, Potential Efficacy, and Pharmacokinetics of PZ-601 in the Treatment of Complicated Skin and Skin Structure Infection

ClinicalTrials.gov ID: NCT00671580

Public ClinicalTrials.gov record NCT00671580. 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 Sep 30, 2026, 3:42 PM 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 Phase II Randomized, Observer-Blind, Multi-Center Study to Evaluate the Safety, Potential Efficacy, and Pharmacokinetics of Two Dosing Regimens of Intravenous PZ-601 and Standard of Care in the Treatment of Complicated Skin and Skin Structure Infections

Brief summary

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

The purpose of this study is to evaluate the potential effect and safety of two different doses of PZ-601 and to compare this with another antibiotic that is approved by the US Food and Drug Administration (also known as FDA) to treat adults with skin and skin structure infections.

Study identification

NCT ID
NCT00671580
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Protez Pharmaceuticals, Inc.
Industry
Enrollment
99 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 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
May 2008 (Type not available)
Primary completion
Feb 2009 (Actual)
Completion
Feb 2009 (Actual)
Last update posted
Jun 3, 2009

2008 – 2009

United States locations

U.S. sites
15
U.S. states
9
U.S. cities
15
Facility City State ZIP Site status
eStudySite - Sharp Chula Vista Chula Vista California 91911 —
Novellus Research Site Fountain Valley California 92708 —
Novellus Research Site Long Beach California 90806 —
eStudySite - Tri-City Medical Center Oceanside California 92056 —
eStudySite - Good Samaritan Hospital San Jose California 95124 —
Infectious Disease of Indiana, PSC Indianapolis Indiana 46280 —
Gulf Coast Research, LLC Baton Rouge Louisiana 70808 —
Henry Ford Hospital Detroit Michigan 48202 —
University of Missouri Health Care Columbia Missouri 65212 —
Truman Medical Center - Hospital Hill Kansas City Missouri 64108 —
Mercury Street Medical Group Butte Montana 59701 —
Holy Name Hospital Institute for Clinical Research Teaneck New Jersey 07666 —
Summa Health System Akron Ohio 44304 —
Remington-Davis, Inc. Columbus Ohio 43215 —
NewBridge Medical Research Warren Pennsylvania 16365 —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00671580, 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 Jun 3, 2009 · Synced Sep 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00671580 live on ClinicalTrials.gov.

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