A Study of the Safety, Tolerability, Pharmacokinetics and Pharmacodynamic Activity of Very Low Dose-Glucagon in Subjects With Type 1 Diabetes Mellitus

Phase 1

Completed

• Conditions: Type 1 Diabetes

• Registration Number: NCT00304538
• Lead Sponsor: DiObex

Brief Summary

The purpose of this study is to identify the safest dose of very low dose glucagon to prevent hypoglycemia in patients with Type I diabetes who use insulin pumps and to measure the the amount of glucagon in the blood and see how the body responds to the glucagon.

Detailed Description

Glucagon is currently used to treat severe hypoglycemia. DiObex believes that glucagon replacement therapy with very low doses of glucagon may prevent hypoglycemia without compromising effective glycemic control by insulin. In this study very low doses of glucagon will administered to Type I diabetics who use insulin pumps. The glucagon will be administered subcutaneously overnight for 6, 9 or 12 hours to see if the number of mild or impending hypoglycemia events can be safely decreased. Three different doses of glucagon will be compared to a control infusion.

Study Timeline

• Study Start: 2006-03
• Study First Submitted: 2006-03-16
• Study First Submitted QC: 2006-03-16
• Study First Posted: 2006-03-20
• Study Completion: 2006-07
• Status Verified: 2006-08
• Last Update Submitted: 2006-08-21
• Last Update Posted: 2006-08-23

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 10

Inclusion Criteria

1. Males or females, 18 to 55 years of age, requiring daily insulin for the management of type 1 diabetes mellitus for >10 years
2. On a stable basal insulin regimen using CSII therapy ("stable" defined as total daily dose of insulin not changed by more than ± 20% for 2 months prior to screening)
3. Glycosylated hemoglobin (HbA1c) ≤8.0%
4. Total daily insulin requirement of ≤1 unit/kg of body weight
5. Fasting C-peptide level of <1.0 ng/mL (<330 pmol/L) (may be done at screening or may be taken from subject's medical record if performed within the past 12 months)
6. Body mass index (BMI) ≤25.5 kg/m2 and body weight over past 6 months within ± 5%
7. Hemoglobin, hematocrit, and platelets within normal limits; no clinically significant abnormality of white blood cells (WBC) or differential
8. Serum chemistry results within normal limits except for liver enzymes [aspartate transaminase (AST) and alanine transaminase (ALT)] which must be within 2.5 times upper limit of normal (ULN) and creatinine which must be <1.6 mg/dL
9. Normal thyroid stimulating hormone
10. No history of HIV infection and negative results for hepatitis B and C
11. Negative serum pregnancy test, non-lactating, and using adequate contraception, if female and of child bearing potential (intact uterus and pre-menopausal)
12. Medications for the treatment of high blood pressure and/or dyslipidemia are allowed if regimen stable for 2 months prior to screening
13. Medically stable as determined by history and physical examination, including vital signs
14. Electrocardiogram (ECG) shows no acute ischemia or clinically significant abnormality
15. Willing and able to give written informed consent

Exclusion Criteria

1. Participation in a clinical trial with or use of an investigational agent within 30 days of Study Visit 1.
2. History of atherosclerosis including coronary artery disease, angina pectoris, myocardial infarction, cerebrovascular accident, or transient ischemic attacks
3. History or symptoms of pheochromocytoma
4. History of any malignancy within 3 years except for basal cell skin cancer
5. Active infection, drug or alcohol abuse, eating disorder, or psychiatric disorder
6. Concomitant medications: systemic or potent topical steroids or medications that may affect blood glucose, e.g., sulfonylureas, alpha-glucosidase inhibitors, biguanides, meglitinides, thiazolidinediones
7. Any condition which increases the risk of participation in the trial in the opinion of the investigator -

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
1) Evaluate the safety and tolerability of VLD-glucagon in doses of 2, 4 and 8 ng/kg/minute when infused overnight 2) Evaluate the PK profile in plasma of VLD-glucagon 3) Evaluate the pharmacodynamic activity of these doses by measuring glucose levels

Secondary Outcome Measures

Name	Time	Method
Compare the number of times and amount of time subjects have glucose levels < 70 mg/dL when treated with VLD-glucagon vs. the control infusion

Trial Locations

Locations (1)

University Of California, San Diego; 🇺🇸 San Diego, California, United States