A Study to Assess Efficacy and Safety of ASP1941 in Diabetic Patients With Renal Impairment
NCT01316094 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 165
Last updated 2025-05-22
Summary
This study is to assess the effect of renal function on the efficacy and safety of ASP1941 in type 2 diabetic patients with mild to moderate renal impairment.
Conditions
Interventions
- DRUG
-
ASP1941
oral
- DRUG
-
oral
Sponsors & Collaborators
-
Astellas Pharma Inc
lead INDUSTRY
Principal Investigators
-
Central Contact · Astellas Pharma Inc
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- QUADRUPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 20 Years
- Max Age
- 74 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2011-01-18
- Primary Completion
- 2012-11-28
- Completion
- 2012-11-28
Countries
- Japan
Study Locations
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