Enhanced Epidermal Antigen Specific Immunotherapy Trial -1

Type 1 Diabetes Clinical Trial

— EE-ASI-1  

Official title:

Enhanced Epidermal Antigen Specific Immunotherapy Trial -1 (EE-ASI-1): A Phase 1a Study of Gold Nanoparticles Administered Intradermally by Microneedles to Deliver Immunotherapy With a Proinsulin Derived Peptide in Type 1 Diabetes

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02837094
• Other study ID #: SPON1455-15
• Status: Completed
• Phase: Phase 1
• Start date: September 29, 2016
• Est. completion date: December 31, 2019

Study information

• Verified date: January 2021
• Source: Cardiff University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The study is a two centre, open-label, uncontrolled single group phase 1A study of C19-A3 GNP peptide (10 μg peptide equivalent content) administered via Nanopass microneedles every 28 days for 8 weeks (3 doses), with follow-up for 6 weeks (14 weeks in total from first dose). Treatment will be given into the arm at a volume of 50ul. No blinding or randomisation will be performed. In keeping with standard phase 1 study designs, no placebo or control group is included as the primary aim is to establish whether there are any major unexpected safety issues in the use of this IMP for the first time in man. 8 subjects will be recruited at 2 centres: Cardiff, UK and Linköping, Sweden.

Description:

Type 1 Diabetes is caused by the body's own white blood cells damaging the insulin producing cells in the pancreas. The aim is to develop a treatment that can slow or stop this process by switching off the white blood cells causing the damage. The aim of this study is to investigate whether giving such a treatment involving a peptide fragment related to insulin attached to gold nanoparticles is safe with no significant side-effects. Participants need to be: 1. Diagnosed with type 1 diabetes for more than 3 months. 2. Aged between 18 and 40 years. 3. Prescribed insulin within 1 month of diagnosis. Participants will have a blood test to assess whether they have the right tissue type for the study. If suitable, they will be asked to attend their local research centre for a general examination and further blood and urine tests. If the participant still has some insulin response after the post meal urine test they will proceed to the first injection. Each participant will have 3 injections of the same treatment, these are given 4 weeks apart. During the treatment, participants will undergo various monitoring including blood & urine tests, mixed meal tolerance tests, lymph node biopsies. A follow up appointment will take place 6 weeks after the last injection. Possible side effects include bruising and discomfort at the site of the blood test and lymph node tests, local redness and swelling reactions at the site of the injections, severe allergic reaction to the injection requiring treatment, such as steroids, adrenaline or fluids. Participants will have more time with staff members to discuss their diabetes and ask questions than at a routine clinic appointment. It is not known whether receiving the gold particle-peptide injections will be of benefit, as this is the first study where the treatment is being used in humans.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 6
• Est. completion date: December 31, 2019
• Est. primary completion date: December 31, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 16 Years to 40 Years

Eligibility

Inclusion Criteria:

1. Clinical diagnosis of type 1 diabetes for > 3 months (dated from the first insulin injection).

2. Commenced on insulin treatment within 1 month of diagnosis.

3. Age 16 to 40 years

4. 2 hour post-meal UCPCR > 0.53 nmol/mmol on at least one occasion (maximum 3 tests on different days)

5. Possession of 0401 allele at the HLA-DRB1 gene locus

6. The following birth control methods should be used (considered highly effective with a

failure rate of less than 1% per year when used consistently and correctly]:

• combined (estrogen and progestogen containing) hormonal contraception associated

with inhibition of ovulation:

• oral
• intravaginal
• transdermal
• progestogen-only hormonal contraception associated with inhibition of ovulation:
• oral
• injectable
• implantable
• intrauterine device (IUD)
• intrauterine hormone-releasing system (IUS)
• bilateral tubal occlusion
• vasectomised partner (provided that the partner is the sole sexual partner of the trial participant and that medical assessment of azoospermia has been confirmed)
• Sexual abstinence (defined as refraining from hetrosexual intercourse during the duration of the trial)

7. Written and witnessed informed consent to participate. Exclusion criteria

1. HbA1c > 86mmol/L (10%).

2. Females who are pregnant, breast-feeding or not using adequate forms of contraception.

3. Previous diagnosis of renal disease including glomerulonephritis or nephropathy.

4. Raised serum creatinine or abnormal urine albumin/creatinine ratio (ACR) (values above the laboratory reference range). If the initial ACR is raised, this should be repeated on two further occasions as first morning samples. The subject can be included if both of these samples are negative (within the reference range).

5. Use of immunosuppressive or immunomodulatory therapies, including systemic steroids within 1 month prior to receiving the IMP and any monoclonal antibody therapy given for any indication. Note that previous exposure to proinsulin peptide C19-A3 in a clinical trial is an exclusion criterion.

6. Use of cannabis within one month prior to trial entry.

7. Use of any hypoglycaemia agents other than insulin, for more than 6 weeks, at any time prior to trial entry.

8. Use of inhaled insulin.

9. Known alcohol abuse, drug abuse, HIV or hepatitis.

10. Allergies to drug components or any excipients.

11. Any other medical condition which, in the opinion of investigators, could affect the safety of the subject's participation or outcomes of the study, including immunocompromised states and autoimmune conditions.

12. Subjects should not have had immunisations (flu and others) for 1 month prior to trial entry and should not receive any during their time in the trial

13. Recent subject's involvement in other research studies which, in the opinion of investigators, may adversely affect the safety of the subjects or the results of the study.

14. Abnormal ECG findings.

Related Conditions & MeSH terms

• Diabetes Mellitus, Type 1
• Type 1 Diabetes

Intervention

Drug:
• C19-A3 GNP
C19A3 GNP intradermal microinjectable solution of human C19A3 proinsulin peptide coupled to gold.

Locations

Country	Name	City	State
United Kingdom	Cardiff and Vale University Health Board	Cardiff

Sponsors (1)

Lead Sponsor	Collaborator
Cardiff University

Country where clinical trial is conducted

United Kingdom, 

References & Publications (1)

Tatovic D, McAteer MA, Barry J, Barrientos A, Rodriguez Terradillos K, Perera I, Kochba E, Levin Y, Dul M, Coulman SA, Birchall JC, von Ruhland C, Howell A, Stenson R, Alhadj Ali M, Luzio SD, Dunseath G, Cheung WY, Holland G, May K, Ingram JR, Chowdhury M — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To examine the risk of C19A3 GNP administration in terms of general safety and induction of hypersensitivity.	A physical examination will be conducted at screening and 0, 4, 8 and 14 weeks. A review of AEs will be performed at all visits and blood will be drawn at screening, weeks 4, 9, 14 & 20 to examine the full blood count; urea, electrolytes and creatinine; liver function tests; (prothrombin time, total bilirubin, total protein, albumin, AST (SGOT), SGPT (ALT), alkaline phosphatase; thyroid stimulating hormone; immunoglobulins (G, A, M); calcium; magnesium, phosphate, lipid profile (total cholesterol, LDL, HDL, triglyceride). Urinalysis for pH blood, protein, urine beta-2-microglobulin and albumin/creatinine ratio will be done at screening and visits 1, 2, 4, 5 and 6 and urine for cystatin-c will be collected at visits 1, 4, 5 & 6. A urine pregnancy test will be completed in females only, at all trial visits. Induction of hypersensitivity to C19-A3 GNP will be assessed by a period of observation of subjects and during the immediate period after peptide injection.	4 months
Secondary	To study the feasibility of delivering C19A3 GNP via microneedles to humans.	By using the ultra short needles the antigen can be delivered into the superficial layers of the skin reliably with direct (perpendicular) injection. This approach has the advantage that it ensures intradermal rather than subcutaneous delivery ensuring high efficiency. At visits 1, 1b, 3b, 4, 5 and 6 blood and urine samples will be taken for gold concentrations to enable assessment of gold excretion.	4 months
Secondary	To study the immune responses to C19A3 GNP generated in blood.	Measured as follows: T cell responses to C19-A3 GNP as determined by changes from baseline of interferon gamma following treatment.	4 months
Secondary	To study the immune responses to C19A3 GNP generated in the draining (axillary) lymph node.	Measured as follows: T cell responses to C19-A3 GNP as determined by changes from baseline of interferon gamma in draining axillary lymph node before treatment and following the last treatment administration.	4 months

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