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Clinical trial

An Open-label, Multi-center Study to Compare the Relative Bioavailability of Tocilizumab in Healthy Subjects Following Single Dose Subcutaneous (SC) Administration Via Disposable Auto-Injector (DAI) Device vs Pre-filled Glass Syringe (PFS)

NCT01418989 is registered in ClinicalTrials.gov with Hoffmann-La Roche as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
An Open-label, Multi-center Study to Compare the Relative Bioavailability of Tocilizumab in Healthy Subjects Following Single Dose Subcutaneous (SC) Administration Via Disposable Auto-Injector (DAI) Device vs Pre-filled Glass Syringe (PFS)
Lead sponsor
Hoffmann-La Roche
Phase
Phase 1
Overall status
Completed
Start date
July 31, 2011
Completion date
November 30, 2011
Enrollment
239 (actual)
Sites
2

Conditions

As the registry lists them; a condition with its own page is linked.

healthy volunteer