Treatment of Patients With Type 2 Diabetes With an Interleukin-1 Antagonist

Type 2 Diabetes Clinical Trial

Official title:

Phase 2 Study of IL-1Ra in Patients With Type 2 Diabetes

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00303394
• Other study ID #: EK-1000-ZH
• Status: Completed
• Phase: Phase 2
• First received: March 14, 2006
• Last updated: March 2, 2007
• Start date: April 2004
• Est. completion date: March 2006

Study information

• Verified date: March 2007
• Source: University of Zurich
• Contact: n/a
• Is FDA regulated: No
• Health authority: Switzerland: Swissmedic
• Study type: Interventional

Clinical Trial Summary

Aim: To investigate the therapeutic potential of IL-1Ra in type 2 diabetes.

Rationale: Since the major defect leading to a decrease in b-cell mass in type 2 diabetes is increased apoptosis, therapeutic approaches designed to arrest apoptosis could be a significant new development in its management. This approach might actually reverse the disease to a degree rather than just palliate glycemia. Based on current thinking, treatment with IL-1Ra appears as a promising approach. The prospected effect is blocking of the IL-1b-mediated glucotoxicity and thereby to prevent the decline in b-cell mass, together with a rapid restoration of b-cell function. FDA approval for IL-1Ra in the treatment of rheumatoid arthritis occurred based on a favourable tolerability profile.

Description:

Methodology: This will be a two-centre (University Hospital, Zurich, Switzerland and Steno Diabetes Center, Gentofte, Denmark) study. 72 patients will be randomised according to a double-blind, placebo-controlled protocol in which half of the patients are treated with IL-1Ra, the other half with saline. The treatment period will last 13 weeks. This time-period should be sufficient for reversal of functional glucotoxicity and feasible in terms of patient compliance. Whether 13 weeks of treatment will be sufficient to make significant changes in b-cell mass in unpredictable. However, blocking b-cell apoptosis, while new islet formation and b-cell replication are normal, may initiate enlargement of b-cell mass, which may progress beyond the treatment period. Patient evaluation will be performed at start and after 4, 13, 26, 39 and 52 weeks. Following 13 weeks, patients with a fasting plasma glucose levels > 8 mM or with a glycosylated hemoglobin level (HbA1c) > 8% will be treated with insulin. Insulin treatment will not be initiated earlier to avoid interference with possible effects of insulin on primary outcome in the period where the largest effect of IL-1Ra are expected. To assess effects of IL-1Ra on insulin sensitivity, a subset of 40 patients (20 IL-1Ra- and 20 placebo-treated) will undergo an euglycemic-hyperinsulinemic clamp as well as a muscle and fat biopsy at start and after the end of treatment (13 weeks). The Ethics Committee of both centres have already approved the procedure.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 72
• Est. completion date: March 2006
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 20 Years and older

Eligibility

Inclusion Criteria:

• Age >20

• Diabetes mellitus Type 2 (American Diabetes Association criteria) of at least 3 months duration

• HbA1c >7.5%

• Body-mass index (BMI) > 27

Exclusion Criteria:

• Positive GAD 65 or IA-2 antibodies at inclusion.

• HbA1c >12%, polyuria and thirst (exclusion of severely decompensated patients)

• C-peptide < 400pmol/l (basal )

• Established anti-inflammatory therapy (includiung cortisone, NSAID, Cox-2-inhibitor). Low dose aspirin (£ 100mg) will be tolerated.

• CRP >30 mg/dl, fever, current treatment with antibiotics, or chronic granulomatous infections (e.g. tuberculosis) in the history or on a screening chest X-ray.

• Neutropenia or anemia (leucocyte count < 2.0x109 /l, hemoglobin <11g/dl for ma les or <10g/dl for females)

• Pregnancy or breast-feeding. When appropriate (fertile women),anticonception for at last 3 month prior inclusion will be required.

• Severe liver or renal disease ( AST or ALT>3 times the upper limit of normal laboratory range, serum creatinine >130mM)

• Ongoing malignant neoplasm

• Use of any investigational drug within 30 days of enrollment into the study or within 5 half-lives of the investigational drug (whichever is longer)

• Immunosuppressive treatment or immunodeficient diseases.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Diabetes Mellitus, Type 2
• Type 2 Diabetes

Intervention

Drug:
• IL-1Ra

Locations

Country	Name	City	State
Denmark	Steno Diabetes Center	Gentofte	Copenhagen
Switzerland	University Hospital of Zurich, Division of Endocrinology and Diabetes	Zurich

Sponsors (2)

Lead Sponsor	Collaborator
University of Zurich	Steno Diabetes Center

Countries where clinical trial is conducted

Denmark,  Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	HbA1c
Secondary	Insulin requirement
Secondary	Stimulated C peptide and insulin
Secondary	Fasting plasma glucose (FPG)
Secondary	Serum cytokine levels, CRP
Secondary	Insulin secretion and Insulin-sensitivity index derived from an OGTT with insulin and glucose measurements.
Secondary	In a subgroup of patients, insulin-sensitivity assessed by clamp techniques
Secondary	Insulin signaling- and cytokine- gene expression profiles derived from muscle and fat biopsy samples.