← Back to Search

Potassium Channel Activator

Diazoxide + Naloxone for Low Blood Sugar Prevention

Phase 4
Waitlist Available
Led By Meredith Hawkins, MD, MS
Research Sponsored by Albert Einstein College of Medicine
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up every 15 minutes during the first and third 2-hour hypoglycemic episodes (on day 1 and day 2)
Awards & highlights
Drug Has Already Been Approved
Pivotal Trial

Summary

This trial is testing whether two drug treatments can prevent unawareness of hypoglycemia in diabetics and improve the body's response to low blood sugar. Only healthy non-diabetics are being studied.

Who is the study for?
This trial is for healthy, non-diabetic individuals aged 21-55 who don't smoke heavily, have no major organ dysfunction or chronic diseases, aren't heavy drinkers, and have no family history of diabetes or premature cardiac death. Participants should not be on certain medications or enrolled in other medication trials recently.
What is being tested?
The study tests if naloxone nasal spray and diazoxide can prevent Hypoglycemia Associated Autonomic Failure (HAAF) in people at risk. It has three phases: identifying at-risk individuals; testing naloxone vs placebo; and combining naloxone with diazoxide versus placebos.
What are the potential side effects?
Potential side effects from the interventions may include mild to moderate reactions such as nausea, headache, dizziness, or local irritation from the nasal spray. Diazoxide could cause fluid retention or changes in blood sugar levels.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~every 15 minutes during the first and third 2-hour hypoglycemic episodes (on day 1 and day 2)
This trial's timeline: 3 weeks for screening, Varies for treatment, and every 15 minutes during the first and third 2-hour hypoglycemic episodes (on day 1 and day 2) for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Difference in peak epinephrine levels between first and third hypoglycemic episodes
Secondary study objectives
Endogenous glucose production (EGP)
Symptoms of low blood sugar (hypoglycemia)

Awards & Highlights

Drug Has Already Been Approved
The FDA has already approved this drug, and is just seeking more data.
Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.

Trial Design

7Treatment groups
Experimental Treatment
Active Control
Placebo Group
Group I: Naloxone + diazoxideExperimental Treatment2 Interventions
Naloxone/Diazoxide evaluation: Up to 7 mg/kg oral diazoxide 3 hours before the first hypoglycemic episode. Intranasal naloxone (4 mg NARCAN Nasal Spray) via a nostril twice during the first hypoglycemia episode; once at the start of insulin administration and again after one hour. Intranasal naloxone (4 mg NARCAN Nasal Spray) will again be given via a nostril twice during the second period of hypoglycemia; once at the start of insulin administration and again after one hour.
Group II: NaloxoneExperimental Treatment1 Intervention
Naloxone evaluation: Intranasal naloxone (4 mg NARCAN Nasal Spray) via a nostril twice during the first hypoglycemia episode; once at the start of insulin administration and again after one hour. Intranasal naloxone (4 mg NARCAN Nasal Spray) will again be given via a nostril twice during the second period of hypoglycemia; once at the start of insulin administration and again after one hour.
Group III: No intervention (Susceptibility to HAAF evaluation)Active Control1 Intervention
Susceptibility to HAAF evaluation: No intervention medication will be given during episodes of hypoglycemia.
Group IV: Diazoxide + placebo (for naloxone)Active Control2 Interventions
Naloxone/Diazoxide evaluation: Up to 7 mg/kg oral diazoxide 3 hours before the first hypoglycemic episode. Placebo (for naloxone) nasal spray via a nostril twice during the first hypoglycemia episode; once at the start of insulin administration and again after one hour. Placebo (for naloxone) nasal spray will again be given via a nostril twice during the second period of hypoglycemia; once at the start of insulin administration and again after one hour.
Group V: Naloxone + placebo (for diazoxide)Active Control2 Interventions
Naloxone/Diazoxide evaluation: Oral placebo (for diazoxide) 3 hours before the first hypoglycemic episode. Intranasal naloxone (4 mg NARCAN Nasal Spray) via a nostril twice during the first hypoglycemia episode; once at the start of insulin administration and again after one hour. Intranasal naloxone (4 mg NARCAN Nasal Spray) will again be given via a nostril twice during the second period of hypoglycemia; once at the start of insulin administration and again after one hour.
Group VI: Placebo (for Naloxone)Placebo Group1 Intervention
Naloxone evaluation: Placebo (for naloxone) nasal spray via a nostril twice during the first hypoglycemia episode; once at the start of insulin administration and again after one hour. Placebo (for naloxone) nasal spray will again be given via a nostril twice during the second period of hypoglycemia; once at the start of insulin administration and again after one hour.
Group VII: Placebo (for naloxone) + placebo (for diazoxide)Placebo Group2 Interventions
Naloxone/Diazoxide evaluation: Oral placebo (for diazoxide) 3 hours before the first hypoglycemic episode. Placebo (for naloxone) nasal spray via a nostril twice during the first hypoglycemia episode; once at the start of insulin administration and again after one hour. Placebo (for naloxone) nasal spray will again be given via a nostril twice during the second period of hypoglycemia; once at the start of insulin administration and again after one hour.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Naloxone
2014
Completed Phase 3
~1290
Diazoxide
2006
Completed Phase 4
~80

Find a Location

Who is running the clinical trial?

National Institutes of Health (NIH)NIH
2,810 Previous Clinical Trials
8,159,615 Total Patients Enrolled
25 Trials studying Diabetes
64,177 Patients Enrolled for Diabetes
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)NIH
2,439 Previous Clinical Trials
4,324,807 Total Patients Enrolled
109 Trials studying Diabetes
138,677 Patients Enrolled for Diabetes
Albert Einstein College of MedicineLead Sponsor
296 Previous Clinical Trials
11,784,311 Total Patients Enrolled
4 Trials studying Diabetes
684 Patients Enrolled for Diabetes

Media Library

Diazoxide (Potassium Channel Activator) Clinical Trial Eligibility Overview. Trial Name: NCT03608163 — Phase 4
Diabetes Research Study Groups: Placebo (for Naloxone), Placebo (for naloxone) + placebo (for diazoxide), Naloxone + diazoxide, No intervention (Susceptibility to HAAF evaluation), Naloxone, Diazoxide + placebo (for naloxone), Naloxone + placebo (for diazoxide)
Diabetes Clinical Trial 2023: Diazoxide Highlights & Side Effects. Trial Name: NCT03608163 — Phase 4
Diazoxide (Potassium Channel Activator) 2023 Treatment Timeline for Medical Study. Trial Name: NCT03608163 — Phase 4
~2 spots leftby Nov 2025