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Clinical Trials/NCT01240759
NCT01240759
Completed
Phase 2

A Phase 2, Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study of S-707106 in Subjects With Type 2 Diabetes Mellitus and Inadequate Glycemic Control With Metformin Therapy

Shionogi1 site in 1 country218 target enrollmentOctober 2010

Overview

Phase
Phase 2
Intervention
S-707106 Dose A
Conditions
Type 2 Diabetes Mellitus
Sponsor
Shionogi
Enrollment
218
Locations
1
Primary Endpoint
Change from Baseline to Week 12 in Hemoglobin A1c (HbA1c)
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The purpose of this study is to evaluate the safety and efficacy of S-707106 co-administered with metformin in subjects with type 2 diabetes mellitus.

Detailed Description

Based on the unmet clinical need for more safe and effective type 2 diabetes mellitus therapies, together with the nonclinical efficacy and safety profile of S-707106, Shionogi USA, Inc. is initiating studies to further assess the efficacy, clinical pharmacology and safety profile of S-707106 in preparation for full clinical development as a novel treatment for type 2 diabetes mellitus. It is anticipated that S-707106 will provide clinicians and patients with a new therapeutic option to treat type 2 diabetes mellitus with potential advantages over existing therapy.

Registry
clinicaltrials.gov
Start Date
October 2010
End Date
January 2012
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Shionogi
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Subjects with type 2 diabetes mellitus receiving a stable dose of metformin for the past 3 months (with no other medication for glycemic control) and who are clinically stable as determined by medical history
  • Body mass index (BMI) ≥25.0 and \<45.0 (kg/m2) using http://www.bmicalculator.org/ as the BMI calculator
  • No clinically significant abnormal laboratory tests as determined by the investigator except Hemoglobin A1c level ≥7.5% and ≤11.0% and C peptide level \>1.0 ng/mL

Exclusion Criteria

  • Type 1 diabetes mellitus or gestational diabetes mellitus within last 6 months
  • Use of any medication for glycemic control other than metformin during the past 3 months or thiazolidinediones within the past year
  • Congestive heart failure as defined by New York Heart Association class III or IV
  • Fasting glucose \>270 mg/dL
  • Creatinine clearance is \<60 mL/minute
  • History of myocardial infarction within the past 3 months, history of clinically significant cardiac arrhythmia, clinically significant hypotension or hypertension, or clinically significant abnormal electrocardiogram as determined by the investigator

Arms & Interventions

S-707106 Dose A

One S-707106 A tablet + 3 Placebo A tablets

Intervention: S-707106 Dose A

S-707106 Dose A

One S-707106 A tablet + 3 Placebo A tablets

Intervention: Placebo A tablet

S-707106 Dose A

One S-707106 A tablet + 3 Placebo A tablets

Intervention: Metformin

S-707106 Dose B

One S-707106 B tablet + 3 Placebo A tablets

Intervention: S-707106 Dose B

S-707106 Dose B

One S-707106 B tablet + 3 Placebo A tablets

Intervention: Placebo A tablet

S-707106 Dose B

One S-707106 B tablet + 3 Placebo A tablets

Intervention: Metformin

S-707106 Dose C

S-707106 Dose C = Four S-707106 B tablets

Intervention: S-707106 Dose C

S-707106 Dose C

S-707106 Dose C = Four S-707106 B tablets

Intervention: Metformin

Metformin

The standard of care dose of metformin for the individual patient + 3 Placebo A tablets

Intervention: Placebo A tablet

Metformin

The standard of care dose of metformin for the individual patient + 3 Placebo A tablets

Intervention: Metformin

Outcomes

Primary Outcomes

Change from Baseline to Week 12 in Hemoglobin A1c (HbA1c)

Time Frame: Baseline and at 12 weeks

Hemoglobin A1c

Secondary Outcomes

  • Sparse pharmacokinetic assessments(5 days)
  • Change from Baseline at Week 12 in: Fasting plasma glucose, 1,5-Anhydroglucitol, Fructosamine, Glycoalbumin, C-peptide, Beta-cell function and insulin resistance indices using Homeostatic Model Assessment, and Postprandial glucose test(Baseline and at 12 weeks)
  • Safety assessments(5-6 months)
  • Serial pharmacokinetic (PK) assessments(5 days)
  • Percent of subjects with Hemoglobin A1c < 7.0% at Week 12(12 weeks)

Study Sites (1)

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