drugset / Trial / NCT02079545
Bioavailability and Pharmacokinetics Study of Sirukumab in Healthy Male Participants
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Sirukumab | Monoclonal antibody | 50 mg | Intravenous |
| Subject | Sirukumab | Monoclonal antibody | 100 mg | Intravenous |
Indications
No indication recorded.