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NCT01433393 Clinical Trial

Double-blind Comparative Study of TAK-875

Diabetes Mellitus Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01433393
Other study ID # TAK-875/CCT-003
Secondary ID U1111-1124-1518J
Status Completed
Phase Phase 3
First received September 12, 2011
Last updated November 7, 2012
Est. completion date September 2012

Study information
Verified date November 2012
Source Takeda
Contact n/a
Is FDA regulated No
Health authority Japan: Ministry of Health, Labor and Welfare
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the efficacy and safety of treatment with TAK-875 in diabetic patients.

Recruitment information / eligibility
Status Completed
Enrollment 192
Est. completion date September 2012
Est. primary completion date September 2012
Accepts healthy volunteers
Gender Both
Age group 20 Years and older
Eligibility Inclusion Criteria:

1. The participant is an outpatient.

2. The participant signs and dates a written, informed consent form and any required privacy authorization prior to the initiation of any study procedures.

Exclusion Criteria:

1. The participant has any serious cardiac disease, serious cerebrovascular disorder, or any serious pancreatic or hematological disease.

2. The participant is considered ineligible for the study for any other reason by the investigator or sub-investigator.

Study Design

Intervention Model: Parallel Assignment

Related Conditions & MeSH terms

Intervention

Drug:
• TAK-875

• TAK-875

• Placebo

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Takeda

Country where clinical trial is conducted

Japan, 

Outcome
Type Measure Description Time frame Safety issue
Primary HbA1c No
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