Safety and Efficacy of CEM-102 Compared to Linezolid in Acute Bacterial Skin Infections
Status: | Completed |
---|---|
Conditions: | Skin Cancer, Skin and Soft Tissue Infections |
Therapuetic Areas: | Dermatology / Plastic Surgery, Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 4/21/2016 |
Start Date: | August 2009 |
End Date: | March 2010 |
A Phase 2, Randomized, Double-blind, Multi-center Study to Evaluate the Safety and Efficacy of CEM-102 Compared to Linezolid in the Treatment of Acute Bacterial Skin Structure Infections
The purpose of this study is to determine the safety and efficacy of CEM-102 compared to
Linezolid in the treatment of acute bacterial skin structure infections (ABSSIs).
Linezolid in the treatment of acute bacterial skin structure infections (ABSSIs).
ABSSIs are common and affect all age groups. In recent years, ABSSIs caused by multi-drug
resistant pathogens, especially methicillin-resistant Staphylococcus aureus (MRSA) have
become more common. There is an urgent need for additional antibacterial drugs with modes of
action different from those currently available. CEM-102 is one such agent with excellent
activity against S. aureus, including MRSA.
resistant pathogens, especially methicillin-resistant Staphylococcus aureus (MRSA) have
become more common. There is an urgent need for additional antibacterial drugs with modes of
action different from those currently available. CEM-102 is one such agent with excellent
activity against S. aureus, including MRSA.
Inclusion Criteria:
- Diagnosis of acute bacterial skin-structure infection (ABSSI) of no more than 7 days
duration which was suspected or proven to be caused, at least in part, by a
gram-positive pathogen.
- Eligible infections included cellulitis measuring at least 10 cm length and width or
100 cm squared, with or without a focal abscess, and surgical or traumatic wound
infections
- Infection which in the opinion of the investigator will require 10-14 days of
antibacterial therapy.
- Have at least 3 of the following local and/or systemic symptoms and/or signs of
infection: purulent or seropurulent drainage/discharge, erythema, fluctuance,
heat/localized warmth, pain/tenderness to palpation, swelling/induration, regional
lymph node swelling or tenderness, temperature >=100.4 degree F, increased white
blood cell count, or bandemia.
- Must not have received treatment with another systemic antibiotic for the current
ABSSI.
Exclusion Criteria:
- Superficial skin structure infections such as folliculitis, carbuncles, furunculosis,
cutaneous abscesses, and simple cellulitis.
- Infections involving burns, human or animal bites, or chronic diabetic foot ulcers.
- Suspected polymicrobial infection involving Pseudomonas aeruginosa
- Anticipated need for >14 days of antibiotic therapy.
- Infections complicated by the presence of prosthetic materials that will not be
removed, such as permanent cardiac pacemaker battery packs, mesh, or joint
replacement prosthesis.
- Known significant renal, hepatic, or hematologic impairment.
- Received prior potentially effective antimicrobial therapy for the acute bacterial
skin and skin structure infection, unless they were failing therapy after 48 hours or
had a gram-positive pathogen non-susceptible to prior therapy identified as a
causative pathogen.
We found this trial at
15
sites
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials