drugset / Trial / NCT02348879

A Study to Examine the Safety, Pharmacokinetics and Pharmacodynamics of AMG 403 in Healthy Subject

NCT02348879

Phase 1 Completed 51 enrolled Amgen
RandomizedSingle-groupQuadruple-blindTreatment

Summary

This study is to evaluate the safety of AMG 403 in healthy adult subjects. The study consists of a 21 day screening period followed by administration of the investigational product and up to 154 day evaluation period.

Timeline

Start
2005-01
Primary completion
2006-01
Completion
2006-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Fulranumab Monoclonal antibody Subcutaneous

Indications