Safety Study of Intranasal Insulin in Type 1 Diabetes and Diabetic Peripheral Neuropathy

Phase 2

Completed

• Conditions: Diabetic Peripheral Neuropathy
• Interventions: Drug: Novolin Toronto insulin; Drug: Normal saline

• Registration Number: NCT01469559
• Lead Sponsor: University of Calgary

Brief Summary

The aim of this study is to evaluate the safety and tolerability of intranasal insulin in people with type 1 diabetes and diabetic peripheral neuropathy and to determine whether intranasal insulin is effective in slowing the progression of diabetic neuropathy.

Detailed Description

Diabetic polyneuropathy (DPN) is a common complication of human type I and II diabetes mellitus, identified in up to 50% of diabetic subjects regardless of age or type of diabetes. As the global burden of diabetes heightens due to an epidemic of type II diabetes, the prevalence of DPN will concurrently rise. Clinical features of DPN include loss of sensation, propensity towards traumatic wound formation, neuropathic pain, motor weakness and falls.

At this time there is no specific therapy to arrest or reverse DPN. Previous work has demonstrated not only an absolute reduction in plasma insulin levels in Type I diabetes but also in type II diabetics. At the present, therapy for neuropathic pain associated with DPN is available, but only targets symptom relief and is only partially effective.

Intranasal insulin administration is a novel approach to the treatment of diabetic polyneuropathy (DPN) based on robust basic science research. Intranasal insulin is currently being studied in other conditions and has completed Phase II in subjects with cognitive impairment and mild Alzheimer's disease. Intranasal administration of insulin results in increased penetration into the cerebrospinal fluid and the peripheral nervous system while avoiding systemic absorption. Lack of systemic absorption results in maintenance of normal blood glucose levels in normal healthy subjects.

The objectives of the current study are as follows:

1. Primary: To determine the safety and tolerability of intranasal insulin delivery in subjects with type 1 diabetes and DPN.

2. Secondary: To determine whether intranasal insulin is efficacious in slowing the progression of DPN.

This study is designed as a double-blind, placebo-controlled, randomized, controlled-dose escalation phase 2 pilot clinical trial.

The duration of the study for each subject is 11 weeks with 6 weeks of blinded study treatment. The study treatment is either active study drug (Novolin Toronto insulin) or placebo (normal saline).

The phases of the study are as follows:

1. Screening phase (3 weeks): Potential subjects undergo screening procedures to determine eligibility. Procedures include informed consent, review of medical history, anthropometric measures, vital signs, physical examination (including a neurological assessment), and bloodwork.

2. Baseline phase (2 weeks): Eligibility of subjects is confirmed and subjects commence collection of protocol-specified blood glucoses on a daily basis. Nerve conduction tests and corneal confocal microscopy is completed prior to the start of the next phase.

3. Treatment phase (6 weeks): Subjects commence the study treatment at the lowest protocol-specified dose. If assigned to Novolin Toronto insulin, this is 20 international units (IU) twice daily (BID). Return visits to the clinic occur every two weeks for dose escalation. The dose increase is 40 IU BID, then 80 IU BID. Subjects assigned to normal saline receive a volume equivalent to the total volume given to the subjects taking insulin. Visits during the treatment phase also include safety bloodwork, serial blood glucose measurements every 15 minutes for a 2 hour period, review of any hypoglycemia, adverse events, changes to concomitant medications, assessment of neuropathy, questionnaires, teaching, and study treatment accountability/compliance assessment. The study completes at the 11 week time period, immediately prior to which the second nerve conduction study and corneal confocal microscopy is completed.

The study protocol is designed to monitor hypoglycemia throughout the baseline and treatment period for all subjects. Any severe hypoglycemia or significant increases in hypoglycemia (\>30% compared to the baseline phase) will be reviewed by the Investigator on a case-by-case basis to determine continuation with study treatment. Any subject that undergoes discontinuation of study treatment will be continued to be followed to 11 weeks (without study treatment).

Study Timeline

• Study Start: 2011-08
• Study First Submitted: 2011-11-08
• Study First Submitted QC: 2011-11-09
• Study First Posted: 2011-11-10
• Primary Completion: 2012-07
• Study Completion: 2012-07
• Status Verified: 2012-08
• Last Update Submitted: 2012-08-09
• Last Update Posted: 2012-08-10

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 12

Inclusion Criteria

• Patients classified as having type 1 diabetes mellitus according to the Canadian Diabetes Association Criteria.

• Patients clinically defined as having DPN, meeting at least two of the following conditions:

  1. clinical signs of polyneuropathy;
  2. Symptoms of nerve dysfunction;
  3. Nerve conduction deficits in at least 2 nerves.

• Aged 18 through 70 years (inclusive).

• Body Mass Index (BMI) <30 kilograms/meter2.

Exclusion Criteria

• Any other possible etiology contributing to the neuropathy:

  1. History of prolonged untreated hypothyroidism.
  2. Presence of untreated B12 deficiency.
  3. Presence of a paraproteinemia, detected using serum protein electrophoresis with a minimal threshold detection of 2 g/L.
  4. Use of a neurotoxic medication with a clear association with peripheral neuropathy within the past 1 year based upon clinical impression of association.
  5. Previous exposure chemotherapeutic agents with a clear association with peripheral neuropathy at any time.

• History of 2 or more severe hypoglycemic episodes within the previous 6 months.

• History of clustering of hypoglycemia episodes within the previous 12 months.

• History of active or recent (<5 years) malignancy.

• History of systemic or local nasal disease that would complicate the use of intranasal insulin.

• Presence of diabetic nephropathy requiring dialysis.

• Presence of active proliferative retinopathy requiring surgery within 6 months.

• Pregnancy or lactation (female subject of reproductive age must be on contraception).

• Active cardiovascular disease:

  1. Recent angina (<5 years)
  2. Recent myocardial infarction (<5 years)
  3. Congestive heart failure

• Active psychiatric disorder or previous history of psychosis.

• Unable to understand or provide consent.

• Previously documented hypersensitivity to insulin.

• History of hypoglycemia unawareness.

• Glycated hemoglobin < 7.0%.

• Ongoing involvement in another investigational drug trial.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Novolin Toronto insulin	Novolin Toronto insulin	-
Normal saline	Normal saline	-

Primary Outcome Measures

Name	Time	Method
Hypoglycemia monitoring	8 weeks	Hypoglycemia is defined by the development of autonomic or neuroglycopenic symptoms, and with or without the presence of a blood glucose measurement.; All qualifying subjects are provided with blood glucose testing supplies to monitor blood glucoses six times daily from week 3 to week 11 of the study.; Any severe hypoglycemia or increase of hypoglycemia of greater than 30% from the baseline phase (week 3 to week 5) is deemed clinically significant and is reviewed by the investigator to determine subject continuation with study treatment.

Secondary Outcome Measures

Name	Time	Method
Treatment satisfaction questionnaire for medication (TSQM)	6 weeks	The TQSM assesses the overall global impression of the treatment by the study subjects. During the study, the TSQM is administered at weeks 7, 9 and 11.
Electrophysiology	6 weeks	The following components will be measured to monitor changes in nerve conduction: 1. Sural conduction velocity; 2. Radial SNAP amplitude; 3. Radial:Sural SNAP ratio; The nerve conduction tests are completed prior to week 5 (randomization) and immediately prior to week 11 (end of study).
Adverse effects	11 weeks	The subject's overall health is assessed throughout the study to determine any changes with respect to existing history, in addition to capturing any new medical conditions that may arise.
The UTAH early neuropathy scale	6 weeks	The UTAH early neuropathy scale, a standarized physical examination scale, is used to measure changes in sensory neuropathy. During the study, the scale is administered at the time of randomization (week 5), then every 2 weeks until the end of study (week 11).
Corneal confocal microscopy	6 weeks	The corneal confocal microscopy measures corneal nerve fiber branch length and density. This procedure is done prior to week 5 (randomization) and immediately prior to week 11 (end of study).
McGill pain questionnaire	6 weeks	The McGill pain questionnaire, a standardized scale of rating pain on a scale of 0 (no pain) to 10 (worst pain), is used to monitor change in subject's pain symptoms. During the study, subjects complete this questionnaire at week 5 (randomization) and then every 2 weeks until the end of study (week 11).
Short Form-36 (SF-36) Quality of life scale	6 weeks	The SF-36 qualify of life scale, a standardized scale, is used to monitor change in subject reported functionality, well being, and overall health status. During the study, subjects complete this questionnaire at week 5 (randomization) and then every 2 weeks until the end of study (week 11).

Trial Locations

Locations (1)

Heritage Medical Research Clinic; 🇨🇦 Calgary, Alberta, Canada