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Double Blind Comparative Study of TAK-875

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01585792
Enrollment
80
Registered
2012-04-26
Start date
2012-05-31
Completion date
2012-12-31
Last updated
2013-04-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetic Patients

Brief summary

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

Interventions

DRUGGlimepiride
DRUGPlacebo

Sponsors

Takeda
Lead SponsorINDUSTRY

Study design

Primary purpose
TREATMENT

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum

Inclusion criteria

* The participant is an outpatient. * 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

* The participant has any serious cardiac disease, serious cerebrovascular disorder, or any serious pancreatic or hematological disease. * The participant is considered ineligible for the study for any other reason by the investigator or subinvestigator.

Design outcomes

Primary

MeasureTime frameDescription
Blood glucose4 weeksBlood glucose

Countries

Japan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026