drugset / Trial / NCT02570373

A Study to Characterize the Elimination of Guselkumab Glycoform Variants in Healthy Participants

NCT02570373

Phase 1 Completed 8 enrolled Janssen Research & Development, LLC
NaSingle-groupOpen-labelOther

Summary

The purpose of this study is to characterize the elimination of guselkumab glycoform variants following a single intravenous (IV) administration of guselkumab at a 10 milligram per kilogram (mg/kg) dose in healthy participants.

Timeline

Start
2015-09-25
Primary completion
2016-01-12
Completion
2016-01-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Guselkumab Monoclonal antibody 10 mg/kg Intravenous

Indications

No indication recorded.