Overview

A Study of RO4998452 in Type 2 Diabetes Patients With Varying Degrees of Renal Impairment

Status:
Completed
Trial end date:
2010-09-01
Target enrollment:
0
Participant gender:
All
Summary
This 4 arm study will investigate the pharmacodynamics and pharmacokinetics of RO4998452 in type 2 diabetes patients with varying degrees of renal impairment. Eligible patients will be divided into 4 groups, with normal renal function, or mild, moderate or severe renal impairment. All patients will receive a single oral dose of RO4998452 in the fasted state.The anticipated time on study treatment is <3 months (single dose study)and the target sample size is <100 individuals.
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Hoffmann-La Roche
Criteria
Inclusion Criteria:

- adult patients, 40-80 years of age;

- type 2 diabetes;

- normal renal function, or impaired but stable renal function;

- stable with regard to medication or treatment regimen taken for renal impairment or
diabetes.

Exclusion Criteria:

- patients with a renal transplant;

- end-stage renal disease, requiring dialysis;

- nephrotic syndrome, or a history of nephrectomy;

- type 1 diabetes mellitus.