drugset / Trial / NCT02537002

Single Dose Study of PF-05230907 in Healthy Japanese Subjects

NCT02537002 ↗

Phase 1 Completed 17 enrolled Pfizer
RandomizedParallel-groupDouble-blindBasic science

Summary

The purpose of this study is the following: * To determine the safety and tolerability of single ascending intravenous (IV) doses of PF-05230907 in healthy Japanese subjects. * To characterize the PK profile of single ascending IV doses of PF-05230907 in healthy Japanese subjects. * To characterize the PD profiles of single ascending IV doses of PF-05230907 in healthy Japanese subjects. * To evaluate the immunogenicity of PF-05230907 in healthy Japanese subjects

Timeline

Start
2015-09
Primary completion
2016-03
Completion
2016-03

Drugs

EvaluationDrugModalityDoseRoute
Subject PF-05230907 Unknown 3 ug/kg Intravenous
Subject PF-05230907 Unknown 5 ug/kg Intravenous

Indications

No indication recorded.