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OpenTrials
Completed

NCT Number: NCT01632007

Double-blind Comparative Study of SYR-472

The purpose of this study is to evaluate the efficacy and safety of treatment with SYR-472 in diabetic patients.

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Key information

Conditions

Diabetes Mellitus Endocrine System Diseases Glucose Metabolism Disorders Metabolic Diseases Nutritional and Metabolic Diseases

Age range

20 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Akita, Japan

Loading trial locations.

Who can participate

Only the study team can determine whether someone qualifies for participation.

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.（e.g., subjects who require hospitalization or subjects who were hospitalized within 24 weeks prior to the commencement of the observation period)
  • The participant is considered ineligible for the study for any other reason by the investigator or subinvestigator.

Treatment and study plan

SYR-472

Drug

Alogliptin 25 mg

Drug

Other names: SYR-322

Placebo

Drug

Primary outcomes

  1. Glycosylated hemoglobin (HbA1c)

    Time frame: 24 weeks.

    Measurement of change in HbA1c (ratio of hemoglobin bound to glucose).

Sponsors and collaborators

Lead sponsor

Takeda

Industry

Registry information

Important dates

Study start
2012
Primary completion
2013
Study completion
2013
First posted
Jun 29, 2012
Registry last updated
Dec 11, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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