Efficacy and Safety Study of PEX168 in Combination Therapy Diabetes Mellitus Type 2 Patients With Metformin

NCT ID: NCT02477969

Last Updated: 2017-01-24

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE3
• Total Enrollment: 587 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-02-27
• Study Completion Date: 2017-06-30

Brief Summary

This is a multicenter, randomized, double-blind, placebo-controlled, phase III clinical study that will enroll approximately 564 T2DM patients who before screening have inadequately controlled blood glucose （7.0%≤HbA1c≤10.5% at randomization）despite at least 8 weeks of metformin monotherapy at stable doses（≥1500 mg/day).

Detailed Description

Subjects will be randomized to receive either PEX168 100μg, 200μg or PEX 168 Dummy Injection as add-on to metformin hydrochloride. The baseline HbA1c level （HbA1c≤8.5% or HbA1c>8.5）is designed as the stratification factor based on which a dynamic randomization will be performed.

This study consists of 4 periods： Period 1：Up to 3 weeks of screening period. Period 2：A 4-week PEX168 dummy injection run-in period. Period 3：A 52-week treatment period (including a 24-week core treatment period and a 28-week extended treatment period).

Period 4: A 30-day safety follow-up period.

Conditions

Type 2 Diabetes Mellitus

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: TRIPLE

Study Groups

PEX168(100µg)

PEX168,100µg,Subcutaneous injection,once a week. Metformin,0.5mg, tid,oral.

Group Type: EXPERIMENTAL

PEX168(100µg)

Intervention Type: DRUG

PEX168,100µg,Subcutaneous injection,once a week. continued for 52 weeks

Metformin

Intervention Type: DRUG

0.5mg,oral,tid.

PEX168(200µg)

PEX168,200µg,Subcutaneous injection,once a week. Metformin,0.5mg, tid,oral.

Group Type: EXPERIMENTAL

PEX168(200µg)

Intervention Type: DRUG

PEX168,Subcutaneous injection,once a week. continued for 52 weeks

Metformin

Intervention Type: DRUG

0.5mg,oral,tid.

Placebo

Placebo,0.5ml,Subcutaneous injection,once a week. Metformin,0.5mg, tid,oral.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

0.5ml,Subcutaneous injection,once a week.continued for 24 weeks,then followed by PEX168 100µg,qw sc. or 200µg qw sc.for 28 weeks.

Metformin

Intervention Type: DRUG

0.5mg,oral,tid.

Interventions

PEX168(100µg)

PEX168,100µg,Subcutaneous injection,once a week. continued for 52 weeks

Intervention Type: DRUG

PEX168(200µg)

PEX168,Subcutaneous injection,once a week. continued for 52 weeks

Intervention Type: DRUG

Placebo

0.5ml,Subcutaneous injection,once a week.continued for 24 weeks,then followed by PEX168 100µg,qw sc. or 200µg qw sc.for 28 weeks.

Intervention Type: DRUG

Metformin

0.5mg,oral,tid.

Intervention Type: DRUG

Other Intervention Names

Polyethylene Glycol Loxenatide; Polyethylene Glycol Loxenatide; PEGylated Loxenatide Injection Mimetics; ge hua zhi

Eligibility Criteria

Inclusion Criteria

1. Type 2 diabetes mellitus confirmed by the 1999 WHO criteria

2. Men or women

3. Age at signing the ICF≥18 years and ≤78 years

4. Body mass index (BMI) 20-40 Kg/m2

5. At least 8 weeks of metformin monotherapy received prior to screening

6. No glucose-lowering medications other than metformin received within the 8 weeks prior to screening

7. 7.5%≤HbA1c≤11.0% at screening（local or centralized test 7.0%≤HbA1c≤10.5% at randomization (centralized test)

8. Ability to understand the procedures and approach of this study, willingness to complete the study in strict compliance with the protocol and to voluntarily sign the ICF

Exclusion Criteria

1. Investigator suspecting the subject of allergy to the study drug

2. Use of any of the following medications or therapies prior to screening

• GLP-1 receptor agonists, GLP-1 analogues, DPP-4 inhibitors or any other incretin analogues
• Growth hormone therapy within the 6 months prior to screening
• History of drug abuse or alcohol abuse
• Participation in any clinical trial for a pharmaceutical product or medical device within the 3 months prior to screening
• Prolonged (for at least 7 consecutive days) intravenous, oral or intraarticular treatment with corticosteroids within the 2 months prior to screening
• Use of any weight control agents or surgeries that might lead to unstable weight within the 2 months prior to screening, or subjects currently on a weight loss plan not in the maintenance phase
• Any medications used prior to screening that at the investigator's discretion may confound the interpretation of the efficacy or safety data, or use of any medications that may cause common toxicities to major organs, including Chinese herbal medicine

3. History or evidence of any of the following conditions prior to screening：

• Type 1 diabetes mellitus, single gene mutation DM, DM associated with pancreatic injury， or secondary DM, e.g., DM secondary to Cushing syndrome or acromegalia
• History of hypertension with SBP>160 mmHg and/or DBP>100 mmHg despite glucose-lowering agents at stable dose (for at least 4 weeks)
• History of acute/chronic pancreatitis, history of symptomatic cholecystopathy, and the risk factors for pancreatitis including pancreatic injury
• History of myeloid C-cell carcinoma, history of multiple endocrine neoplasm （MEN） 2A or 2B syndrome, or related familiar history
• Clinically significant gastric emptying disorders, severe chronic gastrointestinal disorders, prolonged treatment with peristalsis stimulants, or gastrointestinal surgery
• History of severe hypoglycemic episode, or severe hypoglycemia without symptoms
• Significant hematological disorders , or any diseases that may lead to hemolysis or unstable RBC
• Severe diabetic complications (e.g., macrovascular and microvascular complications) that in the opinion of the investigator make the subject not suitable to participate in this study
• Tumors of any organ or system that have or have not been treated within the 5 years prior to screening, regardless of whether there is evidence of relapse or metastasis, with the exception of local basal cell carcinoma of the skin
• Coronary angioplasty, coronary stenting, coronary artery bypass, uncompensated heart failure （NYHA Class III or IV）, stroke or transient cerebral ischemic attack, unstable angina, myocardial infarction, and persistent and clinically significant arrhythmia, experienced within the 6 months prior to screening
• Acute metabolic complications (e.g., ketoacidosis, lactic acidosis, hyperosmolar coma) within the 6 months prior to screening
• Thyroid dysfunction treated with unstable therapeutic doses (e.g., thioureas, thyroid hormones) within the 6 months prior to screening
• Blood lipid disorders treated with unstable therapeutic doses (e.g., statins, fibrates) within the 6 months prior to screening
• Any severe trauma or severe infection that may interfere with BG control within the 1 month prior to screening

4. Laboratory indicators meeting any of the following criteria prior to screening (any test meeting the criteria must be repeated within 3 work days for confirmation)

• ALT>2.5×ULN and/or AST>2.5×ULN and/or total bilirubin>2.5×ULN
• Hemoglobin≤100 g/L
• Serum creatinine>1.5×UNL and eGFR < 45 ml/min/1.73 m2 eGFR is calculated as：186.3 ×[（Serum Creatinine（mmol/L）/88.4）]-1.154 × [Age (years)]- 0.203 × 1.223 × 0.742 （Females） or ×1（Males）
• Serum thyroid-stimulating hormone（TSH） out of the reference range that is assessed as clinically significant by the investigator
• Fasting TGL>5.64 mmol/L（500 mg/dl)
• Blood amylase and urine amylase>ULN that is assessed as clinically significant by the investigator
• Any clinically significant laboratory abnormalities that at the investigator's discretion may confound the interpretation of the efficacy or safety data

5. Clinically significant 12-lead ECG abnormalities, e.g., Grade II or III atrial ventricular block （with the exception of right bundle branch block），long QT syndrome or QTc>500ms

6. Blood donation or loss≥400 mL，or receipt of blood donation within the 4 weeks prior to screening

7. Pregnant or lactating women, or men or women of child-bearing potential not willing to take contraceptive measures during the study

8. Any other conditions of the subject that at the investigator's discretion may compound the interpretation of the efficacy or safety data

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 78 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Jiangsu Hansoh Pharmaceutical Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Weiping Jia, MD

Role: PRINCIPAL_INVESTIGATOR

Shanghai the sixth Hospital

Locations

Shanghai sixth People's Hospital

Shanghai, Shanghai Municipality, China

Countries

China

Other Identifiers

PEX168-302

Identifier Type: -

Identifier Source: org_study_id