Iclaprim, a dihydrofolate reductase inhibitor antibiotic in Phase III of clinical development: a review of its pharmacology, microbiology and clinical efficacy and safety

Author:

Huang David B1,Dryden Matthew2

Affiliation:

1. Motif BioSciences, 5 Independence Way, Suite 300 Princeton, NJ 08540, USA; Rutgers New Jersey Medical School, 5 Independence Way, Suite 300 Princeton, NJ 08540, USA

2. Department of Microbiology & Infection, Hampshire Hospitals NHS Foundation Trust, Romsey Road, Winchester, Hampshire, SO22 5DG, UK

Abstract

Iclaprim is under clinical development for treating acute bacterial skin and skin structure infections (ABSSSI) and nosocomial pneumonia most often due to Gram-positive bacteria, including infections due to drug-resistant bacteria. In two recent Phase III studies of patients with acute bacterial skin and skin structure infections, intravenous iclaprim 80 mg every 12 h was noninferior to dose-adjusted vancomycin. Additional studies are planned for patients with nosocomial pneumonia. Iclaprim represents an alternative for the treatment of severe skin and pulmonary infections due to Gram-positive bacteria.

Publisher

Future Medicine Ltd

Subject

Microbiology (medical),Microbiology

Reference28 articles.

1. US Centers for Disease Control and Prevention. Antibiotic resistance threats in the United States (2013). www.cdc.gov/drugresistance/pdf/ar-threats-2013–508.pdf.

2. Bacteriophage therapy: a potential solution for the antibiotic resistance crisis

3. The Antimicrobial Resistance Crisis: Causes, Consequences, and Management

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