A Randomized, Open-Label, Active-Controlled, Parallel-Group, Multicenter Study to Determine the Safety and Efficacy of Albiglutide Administered in Combination With Insulin Glargine as Compared With the Combination of Insulin Glargine and Preprandial Lispro Insulin in Subjects With Type 2 Diabetes Mellitus
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 586
- 试验地点
- 1
- 主要终点
- Change From Baseline (BL) in Glycosylated Hemoglobin (HbA1c) at Week 26
研究概览
简要总结
This study will examine the safety and efficacy of albiglutide in combination with insulin glargine as compared with the combination of insulin glargine and preprandial lispro insulin in subjects with type 2 diabetes.
详细描述
This randomized, open-label, active-controlled, parallel-group, multicenter study evaluates the safety and efficacy of a weekly subcutaneously injected dose of albiglutide in combination with insulin glargine as compared with the combination of insulin glargine and preprandial lispro insulin in subjects with type 2 diabetes. Subjects with a historical diagnosis of type 2 diabetes who are inadequately controlled despite the use of insulin glargine or other intermediate- or long-acting insulins for >/= 6 months but < 5 years, with or without oral antidiabetic medications, who are unable to achieve a glycosylated hemoglobin value of < 7% will be recruited into the study. Subjects must also be willing and capable of pursuing an intensive regimen of both basal and preprandial insulin.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Subjects with type 2 diabetes, currently treated with insulin glargine or other intermediate- or long-acting insulin, with or without oral antidiabetic medications, but experiencing inadequate glycemic control and willing and capable of participating in a regimen of intensive insulin administration. A subject who has been on an intermediate- or long acting insulin for >/=6 months but <5 years, and, in spite of dosage adjustments based on home blood glucose monitoring, is unable to achieve a HbA1c of <7%.
- •BMI >/= 20kg/m2 and </=45 kg/m2
- •Fasting C-peptide >/=0.8 ng/mL (>/= 0.26 nmol/L)
- •HbA1c between 7.0% and 10.5%, inclusive
- •Use of oral or systemically injected glucocorticoids is generally not allowed within 3 months before randomization; inhaled, intra articular, and topical corticosteroids are allowed
- •Hemoglobin </=11 g/dL for male subjects and >/=10 g/dL for female subjects
- •Creatinine clearance >60 mL/min (calculated using the Cockcroft Gault formula)
- •Thyroid stimulating hormone level is normal or clinically euthyroid as demonstrated by further thyroid tests (e.g., T4, T3, thyroid-binding globulin)
- •Female subjects of childbearing potential (i.e., not surgically sterile and/or not postmenopausal) must be practicing adequate contraception. Adequate contraception must be practiced for the duration of participation in the study including the 8 week Posttreatment Follow-up Period
- •Able and willing to monitor his or her own blood glucose concentrations with a home glucose monitor as per the protocol recommendations of self administration
- •No major illness or debility that in the investigator's opinion prohibits the subject from actively participating in their diabetes management and completing the study
- •Able and willing to provide written informed consent
排除标准
- •History of cancer, other than squamous cell or basal cell carcinoma of the skin, that has not been in full remission for at least 3 years before Screening.
- •History of treated diabetic gastroparesis
- •Current ongoing symptomatic biliary disease or history of pancreatitis
- •History of significant gastrointestinal surgery, including gastric bypass and banding, antrectomy, Roux en Y bypass, gastric vagotomy, small bowel resection, or surgeries thought to significantly affect upper gastrointestinal function
- •Recent clinically significant cardiovascular and/or cerebrovascular disease including but not limited to the following:
- •Previous history of stroke or transient ischemic attack within 1 month before Screening.
- •Acute coronary syndrome, which includes the following:
- •Documented MI within the 2 months before Screening and during the period up until receiving the first dose of study medication
- •Any cardiac surgery including percutaneous transluminal coronary angioplasty, coronary stent placement, or coronary artery bypass graft surgery within the 2 months before Screening and during the period up until receiving the first dose of study medication
- •Unstable angina not responsive to nitroglycerin within the 2 months before Screening and during the period up until receiving the first dose of study medication
- •Unstable cardiac rhythm, however, as an example, controlled atrial fibrillation is allowed
- •Current or history of heart failure (New York Heart Association class I to IV).
- •Resting systolic pressure is >160 mm Hg and/or diastolic pressure >100 mm Hg.
- •QTc interval (Fridericia) >470 ms confirmed by a central reader at Screening
- •History of stroke or other central nervous system disorder that would negatively impact the subject's ability to participate in a program of intensive insulin management (eg, physically or mentally incapable of performing home blood glucose monitoring or administering and/or adjusting insulin dosage)
- •Hemoglobinopathy that may affect determination of HbA1c
- •History of human immunodeficiency virus infection
- •History of total bilirubin >1.5 × ULN unless the subject has a previously known history of Gilbert's syndrome and a fractionated bilirubin that shows conjugated bilirubin <35% of total bilirubin
- •ALT or aspartate aminotransferase (AST) >2.5 ×ULN
- •Fasting triglyceride level >850 mg/dL at Screening or Week -1 (Visit 5).
- •Acute symptomatic (within 3 months before Screening) infection with hepatitis B or hepatitis C; however, subjects with past or chronic hepatitis B or hepatitis C are allowed provided the requirements for ALT, AST, and total bilirubin are met
- •History of a psychiatric disorder that will affect the subject's ability to participate in the study
- •History of alcohol or substance abuse within 1 year before Screening
- •Positive urine drug screen at Screening, unless the subject is taking a medically approved medication for which a positive drug screen simply verifies the use of this medication
- •Hypoglycemia unawareness which has impaired cognitive function and required outside assistance
- •Female subject is pregnant (confirmed by laboratory testing), lactating, or <6 weeks postpartum
- •Known allergy to any GLP 1 analogue, insulin, other study medications' excipients, excipients of albiglutide, or Baker's yeast
- •Receipt of any investigational drug within the 30 days, or 5 half lives whichever is longer, before Screening or a history of receipt of an investigational antidiabetic drug within the 3 months before randomization, or receipt of albiglutide in previous studies
- •Current use of any GLP 1 analogue
- •History of type 1 diabetes mellitus, diabetic complications (e.g., active proliferative retinopathy or severe diabetic neuropathy) that in the opinion of the investigator would preclude effective participation in the study, or a history of ketoacidosis or hyperosmolar coma
- •Contraindications (as per the prescribing information) for the use of either background or potential randomized study medications (e.g., insulin glargine or lispro insulin)
- •History or family history of medullary carcinoma
- •History or family history of multiple endocrine neoplasia type 2
研究组 & 干预措施
albiglutide + insulin glargine
albiglutide in combination with insulin glargine
干预措施: albiglutide + insulin glargine (Biological)
insulin glargine + preprandial lispro insulin
insulin glargine in combination with preprandial lispro insulin
干预措施: insulin glargine + preprandial lispro insulin (Drug)
结局指标
主要结局
Change From Baseline (BL) in Glycosylated Hemoglobin (HbA1c) at Week 26
时间窗: Baseline and Week 26
HbA1c is a form of hemoglobin that is measured primarily to identify the average plasma glucose concentration over a 2- to 3-month period. The BL HbA1c value is defined as the last non-missing value before the start of treatment. Change from BL was calculated as the value at Week 26 minus the value at BL. The analysis was performed using an Analysis of Covariance (ANCOVA) model with treatment group, region, history of prior myocardial infarction (yes versus no), and age category (\<65 years versus ≥65 years) as factors and Baseline HbA1c as a continuous covariate.The last observation carried forward (LOCF) method was used to impute missing post-BL HbA1c values; the last non-missing post-BL on-treatment measurement was used to impute the missing measurement. HbA1c values obtained after hyperglycemic rescue were treated as missing and were replaced with pre-rescue values.
次要结局
- Change From Baseline in Body Weight at Weeks 36, 48 and 52(Baseline and Weeks 36, 48 and 52)
- Change From Baseline in Fasting Plasma Glucose (FPG) at Week 26(Baseline and Week 26)
- Change From Baseline in Fasting Plasma Glucose (FPG) at Weeks 36, 48 and 52(Baseline and Weeks 36, 48 and 52)
- Number of Participants Who Achieved HbA1c Response Level of <6.5% and <7.0% at Week 26(Week 26)
- Time to Hyperglycemia Rescue(From the start of study medication until the end of the treatment (up to Week 52))
- Change From Baseline in Body Weight at Week 26(Baseline and Week 26)
- Change From Baseline in HbA1c at Weeks 36, 48 and 52(Baseline and Weeks 36, 48 and 52)