Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 4 Interventional

Safety and Efficacy Study of Ceftaroline in Subjects With Staphylococcus Aureus Bacteremia or With Persistent Methicillin-Resistant Staphylococcus Aureus Bacteremia

ClinicalTrials.gov ID: NCT01701219

Public ClinicalTrials.gov record NCT01701219. 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 Jul 21, 2026, 4:34 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 Multicenter, 2-Cohort Study to Describe the Safety and Efficacy of Ceftaroline Fosamil in Subjects With Staphylococcus Aureus Bacteremia or With Persistent Methicillin-Resistant Staphylococcus Aureus Bacteremia

Study identification

NCT ID
NCT01701219
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Forest Laboratories
Industry
Enrollment
56 participants

Conditions and interventions

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
Dec 31, 2012
Primary completion
Apr 30, 2014
Completion
Jun 30, 2014
Last update posted
Jul 30, 2014

2013 – 2014

United States locations

U.S. sites
27
U.S. states
17
U.S. cities
26
Facility City State ZIP Site status
Investigational Site Birmingham Alabama 35294
Investigational Site Sacramento California 95817
Investigational Site San Francisco California 94110
Investigational Site Sylmar California 91342
Investigational Site Torrance California 90502
Investigational Site Hartford Connecticut 06102
Investigational Site Pensacola Florida 32504
Investigational Site Stuart Florida 34994
Investigational Site Decatur Georgia 30030
Investigational Site Macon Georgia 31201
Investigational Site Chicago Illinois 60612
Investigational Site Fort Wayne Indiana 46845
Investigational Site Louisville Kentucky 40202
Investigational Site Boston Massachusetts 02111
Investigational Site Detroit Michigan 48201
Investigational Site Detroit Michigan 48202
Investigational Site Grosse Pointe Woods Michigan 48236
Investigational Site Royal Oak Michigan 48073
Investigational Site Laconia New Hampshire 03246
Investigational Site Neptune City New Jersey 07753
Investigational Site Newark New Jersey 07102
Investigational Site Jamaica New York 11418
Investigational Site Toledo Ohio 43620
Investigational Site Greenville South Carolina 29605
Investigational Site Houston Texas 77030
Investigational Site Annandale Virginia 22003
Investigational Site Roanoke Virginia 24014

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 NCT01701219, 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 Jul 30, 2014 · Synced Jul 21, 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 NCT01701219 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →