drugset / Trial / NCT00757042

Safety Study of Tezepelumab (AMG 157) in Healthy Adults and Adults With Atopic Dermatitis

NCT00757042

Phase 1 Completed 78 enrolled Amgen
RandomizedSequentialDouble-blindTreatment

Summary

This study is a single dose escalation study of tezepelumab (AMG 157) in healthy adults (Part A) and adults with moderate to severe atopic dermatitis (Part B). The purpose of the study is to evaluate the safety, tolerability, immunogenicity and pharmacokinetics of tezepelumab.

Timeline

Start
2008-09-18
Primary completion
2011-01-05
Completion
2011-01-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Tezepelumab Monoclonal antibody 2.1 mg Subcutaneous
Subject Tezepelumab Monoclonal antibody 700 mg Subcutaneous

Indications