EUCTR2008-008732-84-DK
Active, not recruiting
Not Applicable
A Phase IIb, double-blind, parallel group, multi-centre, dose-finding study to investigate the efficacy and safety of 4 doses of MP-513 when added to ongoing metformin monotherapy in subjects with Type 2 diabetes mellitus, with an open label extension
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Type 2 diabetes mellitus
- Sponsor
- Mitsubishi Tanabe Pharma Corporation
- Enrollment
- 400
- Status
- Active, not recruiting
- Last Updated
- 14 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Double\-Blind Treatment Period
- •1\. A signed and dated informed consent form has been obtained from the subject, in accordance with ICH GCP, before any screening or study related procedures take place.
- •2\. The subject is aged \=18 years at signature of the informed consent form.
- •3\. The subject has had a documented diagnosis of Type 2 diabetes for at least 6 months at the screening visit.
- •4\. The subject’s Type 2 diabetes is managed by metformin monotherapy \=1500 mg/day (or \= 1000 mg/day if this is the maximum tolerated dose), plus diet and exercise, as appropriate, and the dose has been unchanged for at least 56 consecutive days at the screening visit.
- •5\. The subject’s HbA1c is \=7\.0 % and \< 10\.0% at the screening visit and Day \-15\.
- •6\. The subject’s BMI is \=20\.0 and \=40\.0 kg/m2 at the screening visit and on Day \-1\.
- •7\. The subject’s C\-peptide is positive (\> 0\.5 nmol/L) at the screening visit.
- •8\. The subject’s FPG at screening visit and on Day \-15 is \<15 mmol/L.
- •9\. Female subjects have a negative serum pregnancy test at the screening visit.
Exclusion Criteria
- •Double\-Blind Treatment Period
- •1\. The subject is suffering from any disease, including Type 2 diabetes or its complications, that in the opinion of
- •the investigator, is sufficiently severe to render the subject unfit, or affect the subject’s ability to participate in the
- •for example:
- •Macroangiopathy with symptoms of coronary heart disease or peripheral
- •arterial obstructive disease.
- •Microangiopathy with symptoms of (autonomous) neuropathy with any
- •one or more of the following: gastroparesis, retinopathy or nephropathy.
- •Symptoms of poor blood glucose control (polyuria, polydipsia or weight
- •2\. The subject has a history of Type 1 diabetes or a secondary form of diabetes.
Outcomes
Primary Outcomes
Not specified
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