Clinical trial
A Multicentre, Randomized, Investigator-blind, Active-controlled Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Efficacy of Ceftobiprole Versus Intravenous Standard-of-care Cephalosporin Treatment With or Without Vancomycin in Pediatric Patients Aged From 3 Months to Less Than 18 Years With Hospital-acquired Pneumonia or Community-acquired Pneumonia Requiring Hospitalisation
NCT03439124 is registered in ClinicalTrials.gov with Basilea Pharmaceutica as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Multicentre, Randomized, Investigator-blind, Active-controlled Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Efficacy of Ceftobiprole Versus Intravenous Standard-of-care Cephalosporin Treatment With or Without Vancomycin in Pediatric Patients Aged From 3 Months to Less Than 18 Years With Hospital-acquired Pneumonia or Community-acquired Pneumonia Requiring Hospitalisation
- Lead sponsor
- Basilea Pharmaceutica
- Phase
- Phase 3
- Overall status
- Completed
- Start date
- November 27, 2017
- Completion date
- March 16, 2020
- Enrollment
- 138 (actual)
- Sites
- 19
Conditions
As the registry lists them; a condition with its own page is linked.
community-acquired pneumonia (cap), hospital-acquired pneumonia (hap)