Efficacy and Safety of Voglibose Compared With Acarbose in Participants With Type 2 Diabetes

NCT ID: NCT02049814

Last Updated: 2019-03-13

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 494 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-05-09
• Study Completion Date: 2016-06-28

Brief Summary

The primary purpose of this study is to evaluate the efficacy of voglibose versus acarbose combined with metformin in participants with type 2 diabetes mellitus (T2DM) by evaluating levels of glycosylated hemoglobin.

Detailed Description

The drug being tested in this study is called voglibose. Voglibose is being tested to treat type 2 diabetes in people who have diabetes that is inadequately controlled on metformin alone. This study will look at glycemic control in people who take voglibose.

The study will enroll 494 patients. All participants will be enrolled in a 2-week screening phase and a metformin run-in phase. Eligible participants will be randomly assigned (by chance, like flipping a coin) to one of the two treatment groups:

• Metformin and Voglibose 0.2 mg
• Metformin and Acarbose 50 mg

All participants will be asked to take their current dose of metformin tablets and either voglibose or acarbose tablets three times a day throughout the study.

This multi-center trial will be conducted in China. The overall time to participate in this study is up to 20 weeks and participants will make 8 visits to the clinic.

Conditions

Type 2 Diabetes Mellitus

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Metformin + Voglibose 0.2 mg

Metformin tablets, at the maximum tolerated dose ≥1000 mg/day, orally, for 12 weeks, in addition to voglibose 0.2 mg, tablets, orally, three times daily, for Weeks 1 and 2, followed by voglibose 0.3 mg, tablets, orally, three times daily, Weeks 3 through 12.

Group Type: EXPERIMENTAL

Metformin

Intervention Type: DRUG

Metformin tablets

Voglibose

Intervention Type: DRUG

Voglibose tablets

Metformin + Acarbose 50 mg

Metformin tablets, at the maximum tolerated dose ≥1000 mg/day, orally, for 12 weeks, in addition to acarbose 50 mg, tablets, orally, three times daily, Weeks 1 and 2, then acarbose 100 mg, tablets, orally, three times daily, Weeks 3 through 12.

Group Type: ACTIVE_COMPARATOR

Metformin

Intervention Type: DRUG

Metformin tablets

Acarbose

Intervention Type: DRUG

Acarbose tablets

Interventions

Metformin

Metformin tablets

Intervention Type: DRUG

Voglibose

Voglibose tablets

Intervention Type: DRUG

Acarbose

Acarbose tablets

Intervention Type: DRUG

Other Intervention Names

Glucophage; Basen; Glucobay, Precose, Prandase

Eligibility Criteria

Inclusion Criteria

1. Has a historical diagnosis of type 2 diabetes mellitus (T2DM) for at least 6 months prior to the screening visit (V1).

2. Is male or female and aged from 18 to 75 years, inclusively.

3. Has a body mass index (BMI) between 20 and 45 kg/m^2, inclusively.

4. Is experiencing inadequate glycemic control with a glycosylated hemoglobin (HbA1c) concentration between 7.0% and 10.0%, inclusively.

5. Has been treated with Metformin for at least 3 months and at a stable dose (≥1000 mg/day) for at least 8 weeks prior to Screening, unless there is documentation that the participant's current dose is his or her maximum tolerated dose (MTD) and MTD is ≤1000 mg/day.

6. Keeps constant body weight with fluctuation range no more than 10% over for at least 3 months before screening.

7. Hemoglobin levels of the participant are ≥12 g/dL (≥120 g/L) in male and≥ 10 g/dL (≥100 g/L) in female at screening visit.

8. Male serum creatinine <1.5 mg/dL and female serum creatinine <1.4 mg/dL, or estimated glomerular filtration rate (eGFR) >60 ml/min/1.73m^2 based on calculation using the Modification of Diet in Renal Disease (MDRD) approximation at Screening.

9. In the opinion of the investigator, the participant is capable of understanding and complying with protocol requirements.

10. The participant or, when applicable, the participant's legally acceptable representative signs and dates a written informed consent form and any required privacy authorization prior to the initiation of any study procedures.

Exclusion Criteria

1. Type 1 diabetes mellitus.

2. Has received insulin, voglibose, acarbose or other oral hypoglycemic drugs (except Metformin) for accumulative total of more than 7 days within the latest 3 months prior to Visit 1.

3. Has a history of cardiovascular disease: acute myocardial infarction, class III or IV heart failure, or cerebrovascular accident (stroke) within the latest 3 months prior to Visit 1.

4. The participant's liver function is damaged and has a significant clinical sign or symptom of hepatopathy, acute or chronic hepatitis, or the value of alanine aminotransferase (ALT) or aspartate aminotransferase (AST) is 3 times more than the upper limit of normal level at Visit 1.

5. Has an active proliferative retinopathy or macular degeneration that need to have an urgent treatment in the opinion of investigators.

6. Has a frequent attack of hypoglycemia or loses consciousness due to hypoglycemia in the opinion of investigators.

7. Has one or more times ketoacidosis or hyperosmotic status/coma.

8. Is receiving long-term (>14days) systemic glucocorticoid treatment (except the medicine: local, intraocular, inhalation or via the nose) or has received such treatment for 4 weeks at Visit 1.

9. Has a hematopathy (e.g. hemolytic anemia, drepanocytosis) that may interfere with the HbA1c test.

10. Has other liabilities (e.g. drug abuse, alcoholism or mental disorder) that may hinder the participant to follow and complete the study.

11. Has participated in another clinical study within the past 90 days or has received any investigational compound within 30 days prior to randomization.

12. Is unsuitable for this study in the opinion of investigators.

13. Has a disease need to use other taboo or caution drugs that is not listed in this study.

14. If female, is pregnant or lactating or intending to become pregnant before, during, or within 30 days after participating in this study.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Takeda

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Medical Director, Clinical Science

Role: STUDY_DIRECTOR

Takeda

Locations

Hefei, Anhui, China

Maanshan, Anhui, China

Beijing, Beijing Municipality, China

Guangzhou, Guangdong, China

Shenzhen, Guangdong, China

Taishan, Guangdong, China

Zhuzhou, Hunan, China

Nanjing, Jiangsu, China

Xuzhou, Jiangsu, China

Changchun, Jilin, China

Jilin, Jilin, China

Shenyang, Liaoning, China

Qingdao, Shandong, China

Shanghai, Shanghai Municipality, China

Yanan, Shanxi, China

Yan’an, Shanxi, China

Tianjin, Tianjin Municipality, China

Wenzhou, Zhejiang, China

Countries

China

Other Identifiers

U1111-1147-3393

Identifier Type: OTHER

Identifier Source: secondary_id

VOG-P4-001

Identifier Type: OTHER

Identifier Source: secondary_id

BASCN1201

Identifier Type: -

Identifier Source: org_study_id