drugset / Trial / NCT02079545

Bioavailability and Pharmacokinetics Study of Sirukumab in Healthy Male Participants

NCT02079545

RandomizedParallel-groupOpen-label

Summary

The purpose of the study is to assess the bioavailability (the extent to which a medication becomes available to the body) of subcutaneously (under the skin using a needle) administered sirukumab and to compare the pharmacokinetics of sirukumab administered subcutaneously using a pre-filled syringe fitted with the UltraSafe Passive™ Delivery system (PFS-U) with the SmartJect™ Autoinjector (PFS-AI) in healthy male participants.

Timeline

Start
2014-03
Primary completion
2015-01
Completion
2015-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Sirukumab Monoclonal antibody 50 mg Intravenous
Subject Sirukumab Monoclonal antibody 100 mg Intravenous

Indications

No indication recorded.