Overview

A Study to Assess Drug-Drug Interaction Between ASP1941 and Miglitol

Status:
Completed
Trial end date:
2010-04-01
Target enrollment:
0
Participant gender:
Male
Summary
This study is to assess the pharmacokinetic interaction between ASP1941 and Miglitol in healthy volunteers.
Phase:
Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Astellas Pharma Inc
Treatments:
1-Deoxynojirimycin
Ipragliflozin
Miglitol
Criteria
Inclusion Criteria:

- Healthy as judged by the investigator/subinvestigator based on the results of physical
examinations and laboratory tests

- Body weight ; ≥50.0 kg, <80.0 kg

- Body Mass Index ; ≥17.6, <26.4

- Written informed consent has been obtained

Exclusion Criteria:

- Received any investigational drugs within 120 days before the screening assessment

- Donated 400 mL of whole blood within 90 days, 200 mL of whole blood within 30 days, or
blood components within 14 days before the screening assessment

- Received medication within 7 days before hospital admission

- A deviation from the assessment criteria of physical examinations or laboratory tests
at screening or upon admission

- History of drug allergies

- With renal, hepatic, gastrointestinal, heart, cerebrovascular or respiratory diseases

- Previous treatment with ASP1941