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Prospective, Interventional, Phase IV Study, Evaluating the Efficacy and Safety of Teicoplanin (100-200 mg, Administered Orally Twice a Day) in Patients With Clostridium Difficile Infection-associated Diarrhea and Colitis

Trial Profile

Prospective, Interventional, Phase IV Study, Evaluating the Efficacy and Safety of Teicoplanin (100-200 mg, Administered Orally Twice a Day) in Patients With Clostridium Difficile Infection-associated Diarrhea and Colitis

Status: Discontinued
Phase of Trial: Phase IV

Latest Information Update: 20 May 2021

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At a glance

  • Drugs Teicoplanin (Primary)
  • Indications Clostridium difficile infections; Colitis; Diarrhoea
  • Focus Therapeutic Use
  • Sponsors Sanofi

Most Recent Events

  • 17 May 2021 Status changed from completed to discontinued with the reason the study was stopped due to COVID-19 and great challenges during patient enrolment period. Current status of this study is far behind the plan. The study cannot be completed according to the plan. Sanofi decides to terminate the study upon comprehensive assessment.
  • 19 Apr 2021 Status changed from recruiting to completed.
  • 13 Aug 2020 Planned End Date changed from 1 Apr 2022 to 1 Oct 2022.

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