Study Comparing Efficacy and Safety of Amaryl M and Metformin Uptitraion to Type 2 DM

Type 2 Diabetes Mellitus Clinical Trial

Official title:

A Multicenter, Randomized, Parallel-group, Open Study to Compare the Efficacy and Safety of Early Combination Therapy With Amaryl M to Metformin Uptitration in Type 2 DM Patients Inadequately Controlled on Metformin HCL

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00612144
• Other study ID #: GLIME_L_02861
• Status: Completed
• Phase: Phase 4
• First received: January 7, 2008
• Last updated: March 26, 2013
• Start date: December 2007
• Est. completion date: May 2009

Study information

• Verified date: March 2013
• Source: Handok Pharmaceuticals Co., Ltd.
• Contact: n/a
• Is FDA regulated: No
• Health authority: Korea: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The aim of this study is to compare the efficacy and safety of early combination therapy with Amaryl M with that of uptitration of metformin monotherapy in patients with type 2 DM inadequately controlled by prior monotherapy with metformin.

Description:

Treatment algorithms for type 2 DM generally employ monotherapy as a first-line pharmacologic treatment option. Disease progression renders monotherapy less effective in controlling blood glucose over time, with approximately half of the patients requiring additional therapy by 3 years after diagnosis. As a result, the use of multiple pharmacologic agents to control blood glucose is well accepted.

In combination therapy, selection of suitable drug may be individualized depending on their health conditions. However, it is advisable to select drugs having different mechanism considering their complimentary action with each other. Therefore, sulfonylureas and metformin HCL is the best combination in which "insulin deficiency" and "insulin resistance", the basic two pathophysiologies in type 2 diabetes could be targeted. The efficacy and safety of the combination with sulfonylureas and metformin HCL have been proven in numerous clinical studies as combination is more effective than monotherapy using each drug in blood glucose control.

Also, new approaches are required in order to attain and maintain good glycaemic control over time and aggressive earlier introduction of combination therapy is being increasingly recommended over conventional stepwise strategies.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 192
• Est. completion date: May 2009
• Est. primary completion date: May 2009
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 30 Years to 75 Years

Eligibility

Inclusion Criteria:

• Ages 30 to 75 at the time of screening visit

• Subjects with type 2 DM diagnosed for at least 3 months before screening

• Subjects with type 2 DM treated with monotherapy of 500mg = metformin = 1000mg for at lest 4 weeks prior to screening

• HbA1c = 7.0% but = 10.0% at the time of screening visit

• 21 kg/m2 = BMI = 40 kg/m2

• A negative pregnancy test for all females of childbearing potential

• Provision of signed and dated informed consent prior to any study procedures

• Ability and willingness to perform SMBG and record the data on the subject's diary

Exclusion Criteria:

• A history of acute metabolic complications such as diabetic ketoacidosis or hyperosmolar nonketotic coma within 3 months before screening

• Current therapy with anti-hyperglycemic agents (except metformin) use in the 4 weeks (8 weeks in case of thiazolidinedione) before screening

• Concomitant treatment prohibited during the study period

• Any oral hypoglycemic agent other than glimepiride, metformin HCl, and fixed-dose combination of glimepiride and metformin HCl

• Any insulin therapy over 7 days consecutively or intermittently in order to treat acute metabolic decompensation or systemic infection during the study

• Intermittent use of systemic corticosteroids or large dose of inhaled steroids

• Subjects with clinically significant renal (serum creatinine level > 1.5 mg/dL in male and > 1.4 mg/dL in female) or hepatic disease (ALT and AST > 2x ULN)

• Clinically significant laboratory abnormality on screening labs or any medical condition that would affect the completion or outcome of the study in the opinion of the investigator and/or sponsor;

• Pregnant or lactating females

• History of drug or alcohol abuse

• Subjects who have a history of noncompliance with regards to follow-up medical care

• Subjects with known hypersensitivity to glimepiride, metformin HCL

• Night-shift workers

• Treatment with any investigational product in the last 3 months before study entry

• Others; subjects who have participated in this study

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Diabetes Mellitus, Type 2
• Type 2 Diabetes Mellitus

Intervention

Drug:
• Glimepiride/metformin fixed combination
Amaryl M 1/250mg~4/1000mg bid for 12~26 weeks Maintenance dose for 10 weeks after 2~14 weeks of dose titration Dose titration according to titration algorithm based on daily mean SMBG
• Metformin HCl
Metformin HCl 500mg~1250mg bid for 12~26 weeks Maintenance dose for 10 weeks after 2~14 weeks of dose titration Dose titration according to titration algorithm based on daily mean SMBG

Locations

Country	Name	City	State
Korea, Republic of	Handok Pharmaceuticals, Co., LTD	Seoul

Sponsors (1)

Lead Sponsor	Collaborator
Handok Pharmaceuticals Co., Ltd.

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Adjusted mean changes in HbA1c from baseline to the last visit		12~24 weeks	No
Secondary	Adjusted mean changes in FPG from baseline to the last visit		12~24 weeks	No
Secondary	Response rate based on HbA1c and FPG levels measured at the last visit		12~24 weeks	No
Secondary	Frequency with hypoglycemic episode		12~24 weeks	Yes
Secondary	Adverse event		12~24 weeks	Yes
Secondary	Abnormal change from baseline in clinical laboratory		12~24 weeks	Yes