drugset / Trial / NCT01423318

A Study of Lebrikizumab in Healthy Japanese and Caucasian Volunteers

NCT01423318

Phase 1 Completed 60 enrolled Genentech, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

This randomized, double-blind, placebo-controlled, parallel-group study will evaluate the safety and pharmacokinetics of subcutaneous lebrikizumab in healthy Japanese volunteers. Healthy Japanese and Caucasian volunteers will be randomized to receive a single subcutaneous dose of either lebrikizumab or placebo.

Timeline

Start
2011-08
Primary completion
2012-02
Completion
2012-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Lebrikizumab Monoclonal antibody Subcutaneous

Indications

No indication recorded.