drugset / Trial / NCT01802853

A Bioavailability and Pharmacokinetic Study of Subcutaneous and Intravenous RO6811135 in Healthy Volunteers

NCT01802853 ↗

Phase 1 Completed 12 enrolled Hoffmann-La Roche
RandomizedCrossoverOpen-label

Summary

This open-label, randomized, 2-way crossover study will assess the absolute bioavailability and pharmacokinetics of RO6811135 in healthy male volunteers. Subjects will be randomized to one of the sequences AB or BA to receive single doses of subcutaneous (A) or intravenous (B) RO6811135, with a washout period of at least 7 days between dosing.

Timeline

Start
2013-05
Primary completion
2013-06
Completion
2013-06

Drugs

EvaluationDrugModalityDoseRoute
Comparator RO6811135 Unknown — Subcutaneous

Indications

No indication recorded.