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CompletedNCT01072331

Pharmacokinetic/Pharmacodynamic Study of MP-513 With Type 2 Diabetes Mellitus

Pharmacokinetic/Pharmacodynamic Study of MP-513 in Japanese Patients With Type 2 Diabetes Mellitus

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
99 (actual)
Sponsor
Tanabe Pharma Corporation · Industry
Sex
All
Age
20 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the effect of MP-513 on 24-h glycemic control in patients with type 2 Diabetes for 4 weeks administration.

Conditions

Interventions

TypeNameDescription
DRUGMP-513MP-513 10 mg, once a day, for 4 weeks
DRUGMP-513MP-513 20 mg, once a day, for 4 weeks
DRUGPlacebo of MP-513MP-513 placebo, once a day, for 4 weeks

Timeline

Start date
2010-02-01
Primary completion
2010-08-01
Completion
2010-08-01
First posted
2010-02-22
Last updated
2026-01-02
Results posted
2012-12-19

Locations

1 site across 1 country: Japan

Source: ClinicalTrials.gov record NCT01072331. Inclusion in this directory is not an endorsement.

Pharmacokinetic/Pharmacodynamic Study of MP-513 With Type 2 Diabetes Mellitus (NCT01072331) · Clinical Trials Directory