The Effect of Saxagliptin on Glucose Fluctuation and Immune Regulation in Patients With Type 1 Diabetes

NCT ID: NCT02307695

Last Updated: 2016-07-06

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE4
• Total Enrollment: 184 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-11-30
• Study Completion Date: 2017-03-31

Brief Summary

To investigate whether saxagliptin could reduce the fluctuation of glycemia and improve the glycemic control in those type 1 diabetes through mechanisms of suppressing glucagon secretion, improving beta cell function, and re-regulating of the T cell immune system.

Detailed Description

Type 1 diabetes mellitus (T1DM) is characterized by immune mediated beta-cell destruction. Due to the imbalance between glucagon and insulin, long-term T1DM patients experience frequent hypoglycaemia and high glucose variability despite of multiple daily injections of insulin.

Dipeptidyl peptidase 4 (DPP-4) inhibitors are a new class of anti-diabetic agents and are widely used in clinical practice to improve glycemic control and protect β-cell function in patients with type 2 diabetes mellitus(T2DM). Saxagliptin, a DPP-4 inhibitor, improves glycemic control in patients with T2DM by increasing endogenous active, intact glucagon-like peptide 1 and glucose-dependent insulinotropic polypeptide in response to food, which augments insulin secretion and decreases glucagon release. This mechanism can lead to the reduction of glucose variation. In some pilot studies, incretin-based therapy in patients with T1DM can improve glucose control and reduce hypoglycemia, the mechanism probably is that it regulates glucagon level. In type 1 diabetic mouse models, DPP-4 inhibitors preserves beta-cell mass and stimulating beta-cell replication.

Interestingly, DPP-4 is also known as cluster of differentiation antigen 26(CD26).It is expressed on the membrane of many types of lymphocyte, e.g. T, B and natural killer(NK)cells, and is involved in their cellular functions. CD26 plays a key role in many aspects in lymphocyte function beyond its DPP-4 enzymatic activity.These observations make it a promising therapeutic target.

Recently, the attention of saxagliptin has been mainly focused on type 2 diabetes, data in type 1 diabetes is rare. We are going to carry out this phase 4 study to testify our hypothesis that saxagliptin could reduce the fluctuation of glycemia and improve the glycemic control in those type 1 diabetes through mechanisms of suppressing glucagon secretion, improving beta cell function, and re-regulating of the T cell immune system.

Conditions

Type 1 Diabetes

Study Design

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

Study Groups

insulin+Saxagliptin

Patients who have diagnosed type 1 diabetes are assigned to receive Saxagliptin tablets 5 mg and insulin for 24-week.

Group Type: EXPERIMENTAL

Saxagliptin

Intervention Type: DRUG

saxagliptin 5 mg p.o. qd, 24 week

Insulin

Intervention Type: DRUG

Patients will be treated according to routine clinical practice at the discretion of the treating physician.

insulin

Patients who have diagnosed type 1 diabetes only use insulin.

Group Type: ACTIVE_COMPARATOR

Insulin

Intervention Type: DRUG

Patients will be treated according to routine clinical practice at the discretion of the treating physician.

Interventions

Saxagliptin

saxagliptin 5 mg p.o. qd, 24 week

Intervention Type: DRUG

Insulin

Patients will be treated according to routine clinical practice at the discretion of the treating physician.

Intervention Type: DRUG

Other Intervention Names

Onglyza; DPP-IV inhibitor

Eligibility Criteria

Inclusion Criteria

1. Provision of informed consent prior to any study specific procedures;

2. Diagnosed with type 1 diabetes;

3. Men or women who are 12 to 65 years of age at time of consenting upon Visit 1.;

4. Positivity for at least one of the four islet autoantibodies(IA-2A、IAA、GADA、ZnT8A);

5. 6.5% ≤ HbA1c ≤10.0%.

Exclusion Criteria

1. type 2 diabetes；

2. Evidence of chronic or acute complications of diabetes which is unstable and requires hospitalization；

3. Evidence of disease stress；

4. History of administration of any antihyperglycemic therapy (other than insulin) during the 12 weeks prior to Visit 1；

5. Have a history of, or currently have, acute or chronic pancreatitis；

6. Immunocompromised individuals such as patients that have undergone organ transplantation or patients diagnosed with HIV or patients with agranulocytosis；

7. Evidence of chronic or acute infection；

8. Active liver disease and/or significant abnormal liver function defined as Aspartate transaminase(AST) ≥3x Upper Limit of Normal(ULN) and/or Alanine aminotransferase (ALT) ≥3x Upper Limit of Normal(ULN)；

9. History of unstable or rapidly progressing renal disease, creatinine clearance(CrCl) ≤50ml/min;

10. Congestive heart failure defined as New York Heart Association (NYHA) class III or IV and/or left ventricular ejection fraction of ≤ 40%；

11. Rheumatoid arthritis or other autoimmune disease(except AITD);

12. Hypersensitivity to saxagliptin；

13. History of drug allergy or allergic disease

14. History of alcohol abuse, illegal drug abuse, mental disease or other disease which is not eligible for the study

15. Pregnant or breastfeeding patients；

16. Patients with any diseases which in the judgement of the investigator would compromise the patient's safety or successful participation in the clinical study

17. Any condition where, in the opinion of the investigator, participation in this study may pose a significant risk to the patient or could render the patient unable to successfully complete the study

18. Any disease or condition which the investigator feels would interfere with the trial;

19. Treatment with other immunosuppressive agent such as systemic glucocorticoids other than replacement therapy. Inhaled, local injected and topical use of glucocorticoids is allowed during the last 90 days prior to Visit 1;

20. Participation in a clinical study during the last 90 days prior to Visit 1;

21. Patients who are participating in other clinical study;

22. Treatment with strong cytochrome P450 3A4/5 (CYP3A4/5) inhibitors or other contraindications to therapy as outlined in the saxagliptin package insert;

23. History of haemoglobinopathies (sickle cell anaemia or thalassemias, sideroblastic anaemia).

• Minimum Eligible Age: 12 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Nanjing Medical University

OTHER

Sponsor Role: lead

Responsible Party

Yang Tao

Department of Endocrinology & Metabolism

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Tao Yang, MD/PhD

Role: PRINCIPAL_INVESTIGATOR

First Affiliated Hospital, Nanjing Medical University, China

Locations

First Affiliated Hospital, Nanjing Medical University

Nanjing, Jiangsu, China

Site Status: RECRUITING

Countries

China

Central Contacts

Tao Yang, MD/PhD

Role: CONTACT

yangt@njmu.edu.cn

86-25-83718836 ext. 6466

Facility Contacts

Tao Yang, PhD

Role: primary

yangt@njmu.edu.cn

86-25-83718836 ext. 6466

Other Identifiers

2014-SR-123

Identifier Type: -

Identifier Source: org_study_id