Intranasal Insulin and Its Effect on Postprandial Metabolism in Comparison to Subcutaneous Insulin
Primary Purpose
Type 1 Diabetes Mellitus
Status
Withdrawn
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
aspart
Nasulin™
Sponsored by
About this trial
This is an interventional basic science trial for Type 1 Diabetes Mellitus focused on measuring Type 1 Diabetes, Nasal Insulin, Insulin Deficiency, Insulin-Dependent
Eligibility Criteria
Inclusion Criteria:
- Diagnosis of Type 1 Diabetes
- Age 18-50
- Treatment management of MDI(multiple daily injections) or Insulin Pump
- BMI between 19-30 Kg/M2
- HbA1c less than or equal to 8.0%
- 75 g OGTT (oral glucose tolerance test)study with insulin concentrations >80uU/mL
Exclusion Criteria:
- Active Proliferative Retinopathy
- Active Nephropathy
- Chronic Upper Respiratory Conditions determined by MD
- Pregnant or Lactating Female
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Nasulin™
aspart
Arm Description
Intranasal insulin spray
Subcutaneous administration
Outcomes
Primary Outcome Measures
The primary endpoint is to determine whether intranasal administration of Nasulin™ will stimulate glucose disposal and suppress endogenous glucose production.
Secondary Outcome Measures
Full Information
NCT ID
NCT00850161
First Posted
February 23, 2009
Last Updated
February 12, 2016
Sponsor
CPEX Pharmaceuticals Inc.
1. Study Identification
Unique Protocol Identification Number
NCT00850161
Brief Title
Intranasal Insulin and Its Effect on Postprandial Metabolism in Comparison to Subcutaneous Insulin
Official Title
Intranasal Insulin and Its Effect on Postprandial Glucose Metabolism in Comparison to Subcutaneous Insulin
Study Type
Interventional
2. Study Status
Record Verification Date
February 2016
Overall Recruitment Status
Withdrawn
Why Stopped
Business purposes.
Study Start Date
July 2009 (undefined)
Primary Completion Date
August 2009 (Anticipated)
Study Completion Date
September 2010 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
CPEX Pharmaceuticals Inc.
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to determine if glucose peaks higher and earlier after a meal when a patient is given intranasal insulin instead of conventional insulin treatment.
Detailed Description
Diabetes mellitus is a common metabolic disorder characterized by hyperglycemia which when untreated is associated with microvascular disease. Most people with type 1 diabetes are treated with a combination of long-acting (basal) insulin and short-acting (prandial) insulin administered prior to meals. This necessitates multiple daily injections (>3) which is a significant barrier to long-term compliance and treatment. Intranasal administration of insulin has been developed in an effort to overcome the need for insulin injection prior to meals. The pharmacokinetic properties conferred to insulin by this route of administration suggest that postprandial glucose disposal may be stimulated leading to lower glucose concentrations in comparison to dosing via other routes. We propose to study postprandial glucose turnover in healthy volunteers with Type 1 diabetes to determine the effect of intranasal insulin on glucose disposal. We wish to do so in order to develop a greater understanding of how the different bioavailability timing of intranasal insulin might alter postprandial glucose disposal and suppression of endogenous glucose production. In order to address these questions we will address specific aims:
Peak postprandial glucose disposal is higher and occurs earlier, in the presence of intranasal insulin administration than it is in more conventional forms of insulin dosing.
Peak suppression of endogenous glucose production is greater and occurs earlier, in the presence of intranasal insulin administration than it is in more conventional forms of insulin dosing.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 1 Diabetes Mellitus
Keywords
Type 1 Diabetes, Nasal Insulin, Insulin Deficiency, Insulin-Dependent
7. Study Design
Primary Purpose
Basic Science
Study Phase
Phase 2
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Nasulin™
Arm Type
Experimental
Arm Description
Intranasal insulin spray
Arm Title
aspart
Arm Type
Active Comparator
Arm Description
Subcutaneous administration
Intervention Type
Drug
Intervention Name(s)
aspart
Other Intervention Name(s)
insulin aspart
Intervention Description
Meal-time insulin. Administered subcutaneously based on routine clinical therapy.
Intervention Type
Drug
Intervention Name(s)
Nasulin™
Other Intervention Name(s)
insulin
Intervention Description
100 IU(2 puffs in each nostril)
Primary Outcome Measure Information:
Title
The primary endpoint is to determine whether intranasal administration of Nasulin™ will stimulate glucose disposal and suppress endogenous glucose production.
Time Frame
Blood will be measured at -30, -20, -10, 0, 2, 6, 8, 10, 20, 30, 45, 60, 75, 90, 120, 150, 180, 210, 240, 270, 300, 330 and 360 minutes
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosis of Type 1 Diabetes
Age 18-50
Treatment management of MDI(multiple daily injections) or Insulin Pump
BMI between 19-30 Kg/M2
HbA1c less than or equal to 8.0%
75 g OGTT (oral glucose tolerance test)study with insulin concentrations >80uU/mL
Exclusion Criteria:
Active Proliferative Retinopathy
Active Nephropathy
Chronic Upper Respiratory Conditions determined by MD
Pregnant or Lactating Female
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Adrian Vella, MD
Organizational Affiliation
Mayo Clinic
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
There is no data; study never initiated.
Learn more about this trial
Intranasal Insulin and Its Effect on Postprandial Metabolism in Comparison to Subcutaneous Insulin
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