drugset / Trial / NCT05518695

Evaluate the Pharmacokinetics of BAT2022 in Healthy Chinese Subjects

NCT05518695 ↗

Phase 1 Completed 32 enrolled Bio-Thera Solutions
RandomizedFactorialQuadruple-blindTreatment

Summary

To evaluate the safety and tolerability of BAT2022 in healthy subjects.

Timeline

Start
2022-06-09
Primary completion
2022-11-07
Completion
2022-11-07

Drugs

EvaluationDrugModalityDoseRoute
Subject BAT2022 Unknown 100 mg Intravenous
Subject BAT2022 Unknown 300 mg Intravenous
Subject BAT2022 Unknown 1000 mg Intravenous
Subject BAT2022 Unknown 1500 mg Intravenous

Indications