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Open-label Study of TAK-875

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01433419
First Posted: September 14, 2011
Last Update Posted: March 22, 2013
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Takeda
September 12, 2011
September 14, 2011
March 22, 2013
January 2012
December 2012   (Final data collection date for primary outcome measure)
Adverse events
Same as current
Complete list of historical versions of study NCT01433419 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
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Open-label Study of TAK-875
Not Provided
The purpose of this study is to evaluate the safety and efficacy of treatment with TAK-875 in diabetic patients.
Not Provided
Interventional
Phase 3
Intervention Model: Parallel Assignment
Diabetes Mellitus
Drug: TAK-875
  • Experimental: TAK-875 25 mg
    Intervention: Drug: TAK-875
  • Experimental: TAK-875 50 mg
    Intervention: Drug: TAK-875
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
333
December 2012
December 2012   (Final data collection date for primary outcome measure)

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.
Sexes Eligible for Study: All
20 Years and older   (Adult, Senior)
Not Provided
Contact information is only displayed when the study is recruiting subjects
Japan
 
 
NCT01433419
TAK-875/OCT-003
U1111-1124-1619 ( Registry Identifier: WHO )
JapicCTI-111605 ( Registry Identifier: JapicCTI )
Not Provided
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Takeda
Takeda
Not Provided
Not Provided
Takeda
March 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP
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