drugset / Trial / NCT04003818

Efficacy and Safety of Teicoplanin in CDAD

NCT04003818

Phase 4 Terminated 50 enrolled Sanofi
NaSingle-groupOpen-labelTreatment

Summary

Primary Objective: Explore the efficacy of teicoplanin (100-200 mg administered orally twice a day for 7 to 14 days) in patients with Clostridium difficile infection-associated diarrhea and colitis Secondary Objective: Evaluate the safety of teicoplanin in patients with Clostridium difficile infection-associated diarrhea and colitis

Timeline

Start
2020-05-15
Primary completion
2021-01-21
Completion
2021-03-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Teicoplanin Other / unclassified 100 mg Oral
Subject Teicoplanin Other / unclassified 200 mg Oral