Azithromycin Insulin Diet Intervention Trial in Type 1 Diabetes

NCT ID: NCT03682640

Last Updated: 2018-09-24

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2
• Total Enrollment: 60 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-09-30
• Study Completion Date: 2021-12-31

Brief Summary

Increasing evidences suggest that infections are important etiological factors for the development of Type 1 Diabetes (T1D). The overall hypothesis of the study is that the treatment of children, during the first year after diagnosis of T1D with Azithromycin, combined with repeated episodes of intensified insulin treatment to induce maximal beta-cell rest, and dietician support to promote dietary habits that minimize the likelihood of bacterial reflux from the duodenum to the pancreatic duct, will lead to preservation of beta cell function.

This trial will examine whether the AIDIT protocol initiated within one week from diagnosis could preserve insulin production in children with Type 1 Diabetes.

Detailed Description

The study is a 2-arm, randomized, open, single center, clinical trial. Eligible patients with type 1 diabetes will be randomized to the AIDIT protocol or treatment as usual (TAU).

All patients diagnosed with T1D and included in the study will receive standard of care. In addition, the AIDIT protocol will include 1) treatment with Azithromycin for 52 weeks using a protocol for children with cystic fibrosis, 2) repeated treatments with intensified supervised high dose insulin infusion, and 3) extra advice and support from the study dietician.

1. Azithromycin Azithromycin will be administered orally. Azithromycin will be given three times per week for 52 weeks. The dose will be 500 mg for children with body weight ≥ 30 kg and 250 mg if body weight < 30 kg.

2. Intensified supervised high dose insulin infusions Participants will, in addition to Azithromycin, also be subjected to intensified anti-diabetic treatment to achieve increased beta-cell rest. This will be achieved by insulin lispro given as a supervised iv infusion for 72 hours within one week of diagnosis and by subcutaneous infusion 6-8 hours during one day in study week 5, 9, 13, 17 (±1 week) and 25, 34, 43 (±2 weeks) after inclusion. The intensified treatments will aim to target a blood glucose level of 4.0 ± 0.5 mmol/l. The efficacy of the intended maximal beta cell rest will be evaluated by measurement of plasma glucose and endogenous C-peptide. If C-peptide remains positive during the supervised infusion of insulin lispro this will be interpreted as that the insulin dose needs to be increased at the next treatment occasion to achieve beta-cell rest.

3. Dietician support Participants will receive extra advice and support from the study dietician within the first week after randomization, and after 7 and 17 weeks. Personalized nutritional advice on intake of carbohydrates, fat and protein based on four-day food records will be given to in order to reduce insulin resistance and insulin need in accordance with ISPAD guidelines. By giving nutritional advices on less volume of the meals, especially of the fluid (maximum 300 ml per meal), and by trying to extend the meal time to at least 20 minutes, the reflux into ductus pancreaticus might be reduced.

All patients will be offered an examination of their pancreas with MRI at 0 and 12 months after inclusion. In addition, plasma samples taken at inclusion and after 1.5 and 12 months will be analysed for the presence of cell-free DNA indicating ongoing cell destruction. Cell-specific methylation patterns of this cell-free DNA will be analysed to determine cell-type specific cell death.

The effect of the addition of treatment according to the AIDIT protocol will be evaluated with a Mixed Meal Tolerance Test (MMTT) to explore the effect on preservation of beta-cell function.

Conditions

Diabetes Mellitus, Type 1; Diabetes Mellitus; Metabolic Disease; Glucose Metabolism Disorders; Endocrine System Diseases; Juvenile Diabetes; Insulin Dependent Diabetes; Type 1 Diabetes Mellitus; Inflammation; Diet Modification

Study Design

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

Study Groups

AIDIT protocol

Treatment as usual with the addition of:

i) Azithromycin Monohydrate, three times a week (≥ 48 h between doses) during 52 weeks. 500 mg if body weight ≥ 30 kg, 250 mg if body weight < 30 kg.

ii) Extra intensive insulin treatment periods for maximum beta-cell rest with Insulin lispro (Sanofi). This treatment will be given i.v. for one episode of 72 hours in the first week after inclusion and s.c. on seven 6-8 h occasions during the study year. The dose will be individually titrated to reach target blood glucose 4.0±0.5 mmol/L.

ii) Dietician support; Extra advice and support from the study dietician within the first week after randomization and after 1.5 and 4 months.

Group Type: EXPERIMENTAL

Azithromycin Monohydrate

Intervention Type: DRUG

Azithromycin Monohydrate tablet (Azithromycin Sandoz) or oral suspension (Azithromax).

Insulin Lispro

Intervention Type: DRUG

Solution for intravenous or subcutaneous use

Dietician support

Intervention Type: BEHAVIORAL

Dietary advice

Control

Patients will receive treatment as usual (TAU). All patients will receive standard therapeutic treatment consisting of insulin replacement with insulin analogues aiming for normoglycemia from diagnosis. Rapid acting insulin analogue will be administered via insulin pump (continuous subcutaneous infusion) with access to insulin injections in case of malfunction in the pump system.

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Azithromycin Monohydrate

Azithromycin Monohydrate tablet (Azithromycin Sandoz) or oral suspension (Azithromax).

Intervention Type: DRUG

Insulin Lispro

Solution for intravenous or subcutaneous use

Intervention Type: DRUG

Dietician support

Dietary advice

Intervention Type: BEHAVIORAL

Other Intervention Names

Azithromycin Sandoz; Azithromax; Insulin lispro Sanofi

Eligibility Criteria

Inclusion Criteria

1. Clinically diagnosed Type 1 Diabetes. First injection of insulin maximum ten days prior to inclusion.

2. Must be willing and capable of taking the study drugs, perform tests and follow up as described as judged by the investigator.

3. Signed informed consent and expected cooperation of the patients for the treatment and follow up.

4. Aged 6.00 -15.99 years at inclusion.

5. Females of childbearing potential must agree to avoid pregnancy during the study period (by abstinence from heterosexual intercourse, or by hormonal or barrier contraception) and have a negative urine pregnancy test.

Exclusion Criteria

1. Other diabetes diagnosis than Type 1 diabetes as judged by the investigator

2. Severe ketoacidosis (DKA) with lowest pH <7.1 within 36 hours from diagnosis.

3. Treatment with any oral or injected anti-diabetic medications other than insulin

4. Significantly abnormal haematology results at screening.

5. Participation in other clinical trials with a new chemical entity within the previous 3 months.

6. Obesity at diagnosis (Iso-BMI ≥ 30 kg/m2 according to http://www.rikshandboken-bhv.se).

7. Other autoimmune disease present at inclusion that in the opinion of the investigator would interfere with the study protocol.

8. Celiac disease present at diagnosis.

9. Treatment with medication known to affect glucohomeostasis, i.e. glucocorticoids (inhaled, nasal or skin topic will be accepted), statins, ACE inhibitors.

10. Pregnancy or lactation

11. Known gastro-intestinal malabsorption disorders

12. Abnormalities in ECG or known cardiac disease

13. Known hearing defects

14. Known hypersensitivity to penicillin

15. Inability or unwillingness to comply with the provisions of this protocol

16. Presence of serious disease or condition in patient or family, which in the opinion of the investigator makes the patient non-eligible for the study.

17. Known renal or hepatic impairment

• Minimum Eligible Age: 72 Months
• Maximum Eligible Age: 192 Months
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Göteborg University

OTHER

Sponsor Role: collaborator

Uppsala University

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Gun Forsander, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

The Queen Silvia Children's Hospital /Sahlgrenska University Hospital (SU), Sahlgrenska Academy, Dept of Pediatrics, University of Gothenburg

Locations

The Queen Silvia Children's Hospital / Sahlgrenska University Hospital

Gothenburg, , Sweden

Site Status: RECRUITING

Countries

Sweden

Central Contacts

Olle Korsgren, MD, PhD

Role: CONTACT

olle.korsgren@igp.uu.se

+46176114187

Facility Contacts

Gun Forsander

Role: primary

Other Identifiers

AIDIT

Identifier Type: -

Identifier Source: org_study_id