search
Back to results

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Withdrawn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
CPEX Pharmaceuticals Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - 50 Years (Adult)All SexesDoes not accept healthy volunteers

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

    First Posted
    February 23, 2009
    Last Updated
    February 12, 2016
    Sponsor
    CPEX Pharmaceuticals Inc.
    search

    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    Withdrawn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

    We'll reach out to this number within 24 hrs