Overview
A Study to Assess Drug-Drug Interaction Between ASP1941 and Miglitol
Status:
Completed
Completed
Trial end date:
2010-04-01
2010-04-01
Target enrollment:
0
0
Participant gender:
Male
Male
Summary
This study is to assess the pharmacokinetic interaction between ASP1941 and Miglitol in healthy volunteers.Phase:
Phase 1Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Astellas Pharma IncTreatments:
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