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An Open-label, Multi-centre, Drug-drug Interaction Study to Assess the Effect of Voglibose (0.2mg Tid) on the Pharmacokinetics, Safety and Tolerability of Single Oral Administration of Dapagliflozin (10mg) in Japanese Patients With Type 2 Diabetes

Phase 1
Conditions
Type 2 Diabetes Mellitus
Registration Number
JPRN-jRCT2080221000
Lead Sponsor
AstraZeneca
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Sex
All
Target Recruitment
Not specified
Inclusion Criteria

Already on voglibose treatment with a steady dosage for at least 8 weeks

- Provision of informed consent prior to any study specific procedures

- Diagnosed with type 2 diabetes

Exclusion Criteria

- Having clinically relevant medical history or concurrent disease such as cardiovascular disease, renal disease, retinopathy, hepatic disease and haematological disease.

- The investigator(s) judged that the Subject should not participate in the study according to screening test or medical history.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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