drugset / Trial / NCT04003818
Efficacy and Safety of Teicoplanin in CDAD
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
Outcome
Outcome not reported
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.”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Teicoplanin | Other / unclassified | 100 mg | Oral |
| Subject | Teicoplanin | Other / unclassified | 200 mg | Oral |