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A Prospective, Randomized, Double Dummy, Double Blind, Multinational, Multicenter Trial Comparing the Safety and Efficacy of Sequential (Intravenous/Oral) Moxifloxacin 400 mg OD to Intravenous Piperacillin/Tazobactam 4.0/0.5 g Every 8 Hours Followed by Oral Amoxicillin/Clavulanic Acid Tablets 875/125 mg Every 12 Hours for the Treatment of Subjects With Complicated Skin and Skin Structure Infections

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Trial Profile

A Prospective, Randomized, Double Dummy, Double Blind, Multinational, Multicenter Trial Comparing the Safety and Efficacy of Sequential (Intravenous/Oral) Moxifloxacin 400 mg OD to Intravenous Piperacillin/Tazobactam 4.0/0.5 g Every 8 Hours Followed by Oral Amoxicillin/Clavulanic Acid Tablets 875/125 mg Every 12 Hours for the Treatment of Subjects With Complicated Skin and Skin Structure Infections

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 10 Nov 2021

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At a glance

  • Drugs Moxifloxacin (Primary) ; Moxifloxacin (Primary) ; Amoxicillin/clavulanic acid; Piperacillin/tazobactam
  • Indications Abscess; Bacterial skin diseases; Cellulitis; Diabetic foot ulcer; Escherichia coli infections; Skin and soft tissue infections; Staphylococcal infections; Wound infections
  • Focus Registrational; Therapeutic Use
  • Acronyms RELIEF
  • Sponsors Bayer; Bayer HealthCare

    • Most Recent Events

    • 19 Jul 2019 This trial has been completed in United Kingdom, according to European Clinical Trials Database
    • 06 Jul 2019 Trial has been completed in Hungary, according to European Clinical Trials Database record.
    • 24 Sep 2010 Results from a sub-study in patients with diabetic foot infections were presented at the 46th Annual Meeting of the European Association for the Study of Diabetes.
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