drugset / Trial / NCT03578588

Benapenem PK Phase Ib Multiple-dose Study

NCT03578588 ↗

Phase 1 Completed 12 enrolled Sihuan Pharmaceutical Holdings Group Ltd.
RandomizedSequentialOpen-labelTreatment

Summary

A single-center, randomized, open-label, three-period and three-crossover trial design is adopted in the single-dose pharmacokinetic study. 12adult volunteers, are assigned to 3 groups, B1(250mg), B2 (500mg), and B3 (1000mg). Each group of subjects receive single-dose test drug at different dosages in each period. The tolerability and pharmacokinetic studies are performed simultaneously. Two doses, 250 mg and 500 mg, are proposed for multiple-dose tolerability and pharmacokinetic studies. The subjects are divided into two groups, C1 and C2, 12 subjects in each group, half males and half females. 250 mg group is performed first. Each subject receives only one dose, intravenous drip, once daily, for 7 consecutive days

Timeline

Start
2015-12-14
Primary completion
2016-01-13
Completion
2016-01-13

Drugs

EvaluationDrugModalityDoseRoute
Subject Banapenem Unknown 250 mg Intravenous
Subject Banapenem Unknown 500 mg Intravenous
Subject Banapenem Unknown 1000 mg Intravenous

Indications

No indication recorded.