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GW823093C For The Treatment Of Type 2 Diabetes Mellitus

This study has been terminated.
(Safety issue)
Sponsor:
ClinicalTrials.gov Identifier:
NCT00370942
First Posted: September 1, 2006
Last Update Posted: March 24, 2017
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):
GlaxoSmithKline
  Purpose
This study was designed to find dose response and as extension in treatment of GW823093C.

Condition Intervention Phase
Diabetes Mellitus, Type 2 Drug: GW823093C A Drug: GW823093C B Drug: GW823093C C Phase 2

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Participant, Investigator)
Primary Purpose: Treatment
Official Title: GW823093 Japan Phase IIa Mono

Resource links provided by NLM:


Further study details as provided by GlaxoSmithKline:

Primary Outcome Measures:
  • Efficacy variables Dose response (change from baseline in HbA1c) at stipulated date in each treatment group [ Time Frame: 12 weeks ]

Secondary Outcome Measures:
  • Long term safety variables [ Time Frame: 64 weeks ]

Enrollment: 159
Study Start Date: April 2006
Study Completion Date: November 2006
Primary Completion Date: November 2006 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Placebo Comparator: GW823093C A
A=45 mg
Drug: GW823093C A
A=45 mg
Placebo Comparator: GW823093C B
B=30 mg
Drug: GW823093C B
B=30 mg
Placebo Comparator: GW823093C C
C=15 mg
Drug: GW823093C C
C=25 mg

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   20 Years to 74 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion criteria:

  • Type 2 diabetes mellitus.
  • Managed by diet therapy or receiving treatment with oral anti-diabetic monotherapy (excluding TZD (Thiazolidinediones))

Exclusion criteria:

  • Patients who have metabolic disease judged by investigator as a clinically significance
  • Serious cardiovascular disease or serious hepatic disease
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00370942


Locations
Japan
GSK Investigational Site
Hokkaido, Japan, 051-0005
GSK Investigational Site
Miyagi, Japan, 985-0852
GSK Investigational Site
Tokyo, Japan, 130-0004
GSK Investigational Site
Tokyo, Japan, 160-0017
Sponsors and Collaborators
GlaxoSmithKline
Investigators
Study Director: GSK Clinical Trials GlaxoSmithKline
  More Information

Responsible Party: GlaxoSmithKline
ClinicalTrials.gov Identifier: NCT00370942     History of Changes
Other Study ID Numbers: DPB106652
First Submitted: August 30, 2006
First Posted: September 1, 2006
Last Update Posted: March 24, 2017
Last Verified: March 2017

Keywords provided by GlaxoSmithKline:
GW823093C
diabetes
type 2 diabetes mellitus
DPP-IV inhibitor

Additional relevant MeSH terms:
Diabetes Mellitus
Diabetes Mellitus, Type 2
Glucose Metabolism Disorders
Metabolic Diseases
Endocrine System Diseases