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A Phase III, Multicentre, Randomised, Double-Blind Comparative Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil (600 mg Every 8 Hours) vs Vancomycin Plus Aztreonam in the Treatment of Patients With Complicated Bacterial Skin and Soft Tissue Infections With Evidence of Systemic Inflammatory Response or Underlying Comorbidities.

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Trial Profile

A Phase III, Multicentre, Randomised, Double-Blind Comparative Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil (600 mg Every 8 Hours) vs Vancomycin Plus Aztreonam in the Treatment of Patients With Complicated Bacterial Skin and Soft Tissue Infections With Evidence of Systemic Inflammatory Response or Underlying Comorbidities.

Status: Discontinued
Phase of Trial: Phase III

Latest Information Update: 08 Sep 2017

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At a glance

  • Drugs Ceftaroline fosamil (Primary) ; Aztreonam; Vancomycin
  • Indications Methicillin-resistant Staphylococcus aureus infections; Skin and soft tissue infections
  • Focus Registrational; Therapeutic Use
  • Sponsors AstraZeneca

Most Recent Events

  • 01 Sep 2016 Results published in the Journal of Antimicrobial Chemotherapy
  • 30 Mar 2016 Protocol amended as time frame of primary endpoint changed from 8-15 days to 7- 20 days after the last dose of study drug as reported by ClinicalTrials.gov.
  • 28 Jan 2015 Status changed from recruiting to discontinued as reported by ClinicalTrials.gov record.

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