Clinical trial

Abatacept Combined With Nasal Insulin to Preserve Beta-cell Function in Recently-diagnosed Type 1 Diabetes

Name
2022.079
Description
The goal of this clinical trial is to test whether the combination of two safe immune therapies called abatacept and nasal insulin can preserve pancreas function in recently-diagnosed type 1 diabetes. When type 1 diabetes is first diagnosed, the pancreas is still able to make small amounts of insulin, which helps control glucose levels. Preserving pancreas function can make glucose control easier and reduce the need to use injected insulin. Participants will be asked to inject abatacept under their skin once per week and inhale nasal insulin or nasal placebo using a spray for 10 consecutive days initially and twice per week thereafter. The treatment period is for 48 weeks, with another 48-week follow-up period.
Trial arms
Trial start
2023-02-13
Estimated PCD
2026-02-13
Trial end
2027-02-13
Status
Active (not recruiting)
Phase
Early phase I
Treatment
Abatacept (CTLA4-Ig) and nasal insulin (Humulin R®)
Abatacept injected subcutaneously once per week and nasal insulin inhaled for 10 consecutive days initially and twice per week thereafter
Arms:
Abatacept and nasal insulin
Other names:
Abatacept and nasal insulin
Abatacept (CTLA4-Ig) and nasal placebo (0.9% sodium chloride)
Abatacept injected subcutaneously once per week and nasal placebo inhaled for 10 consecutive days initially and twice per week thereafter
Arms:
Abatacept and nasal placebo
Other names:
Abatacept and nasal placebo
Size
62
Primary endpoint
Beta-cell function at 48 weeks
0 weeks - 48 weeks
Eligibility criteria
Inclusion Criteria: * Age between 6 and 21 years and weight at least 20kg at Visit 1 * Diabetes mellitus diagnosed according to ADA criteria (53) within 100 days of Visit 2 * Presence of at least one antibody against insulin (if \<10 days since starting insulin therapy), GAD, IA2 or ZnT8 * Random C-peptide \>0.3nmol/l, measured by a NATA-accredited pathology laboratory within 2 weeks of Visit 2 * Willing to use CGM for the duration of the study * Demonstrated ability to record home glucose measurements and insulin doses, as judged by the study doctor * Willing to forego other forms of experimental treatment during the study * Fully vaccinated against Covid-19, as recommended by the Australian Technical Advisory Group on Immunisation * Up to date with other vaccinations recommended by the Australian Technical Advisory Group on Immunisation * Willing to postpone any live vaccine immunisations for 3 months after treatment Exclusion Criteria: * Clinical or laboratory evidence of active infection other than localised skin infection, including viral hepatitis, EBV, CMV or tuberculosis * Immunodeficiency or chronic use of immunosuppressive drugs other than topical or inhaled glucocorticoid * Vaccination with live or dead virus within 4 weeks of Visit 2 * History of malignancy * Pregnant or lactating, or of child-bearing potential not using an effective method of contraception * Any pathology of the nasal passages that would preclude safe application of the nasal spray * Any condition that would interfere with study conduct or participant safety
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE2'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'TRIPLE', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR']}}, 'enrollmentInfo': {'count': 62, 'type': 'ESTIMATED'}}
Updated at
2024-04-10

1 organization

1 product

3 indications

Organization
Melbourne Health
Product
Abatacept
Indication
Type 1 Diabetes
Indication
Type 1