drugset / Trial / NCT05685615

PK of BV100 in Patients VABP Suspected or Confirmed to Be Due to CRAB

NCT05685615

Phase 2 Completed 39 enrolled BioVersys AG
RandomizedParallel-groupOpen-labelTreatment

Summary

A multicenter Phase 2 study to evaluate the pharmacokinetics, efficacy, and safety of intravenous BV100 combined with Polymyxin B in adult patients with VABP suspected or confirmed to be due to CRAB

Timeline

Start
2023-04-20
Primary completion
2024-11-01
Completion
2024-12-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Rifabutin Small molecule 200 mg Intravenous
Subject Rifabutin Small molecule 300 mg Intravenous
Background Polymyxin B Peptide 12500 iu/kg Intravenous
Background Polymyxin B Peptide 15000 iu/kg Intravenous

Indications

No indication recorded.