This randomized, double-blind, placebo-controlled, multiple ascending dose study will evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of RO6811135 in patients with type 2 diabetes mellitus. Patients will be randomized to receive either RO6811135 or placebo daily for 2 weeks, with a follow-up examination 2 to 3 weeks after the last dose of study drug.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
56
Unnamed facility
Chula Vista, California, United States
Unnamed facility
Cincinnati, Ohio, United States
Safety: Incidence of adverse events
Time frame: approximately 5 months
Pharmacokinetics: Area under the concentration-time curve (AUC)
Time frame: Day 1 and Day 14
Pharmacodynamics of RO681135: Blood analysis
Time frame: 14 days
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