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Intranasal Glucagon and Energy Balance

Assessing the Effects of Intranasal Glucagon on Energy Balance in Humans

Status
UNKNOWN
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03650582
Acronym
INGEB
Enrollment
20
Registered
2018-08-28
Start date
2017-06-06
Completion date
2018-10-30
Last updated
2018-08-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Keywords

food intake, energy expenditure, central nervous system, appetite

Brief summary

People who are overweight often find it difficult to lose weight through diet and medications because weight loss reduces the amount of energy spent by the body and increases appetite. Glucagon, when given as an injection, reduces appetite and increases the amount of energy spent by the body, even when resting. Based on studies in animals, it does so by working on the brain. However, when gives as an injection it raises blood sugar levels by acting on the liver and therefore it is not used as a weight loss drug. It has previously been shown that hormones such as glucagon, when given as a spray through the nose, can reach the brain with no major effect on the liver. Importantly it does not increase blood sugar. In this study the research team is investigating whether nasal glucagon reduces appetite and increases energy spent by the body compared to a placebo spray. If it does, it may be a potential treatment for losing weight.

Detailed description

Resting energy expenditure, appetite and food intake is being investigated in up to 20 individuals. Participants are their own control in a single-blind, placebo-controlled, crossover design. Participants are admitted after an overnight fast and allowed to rest for 1 hour before either intranasal glucagon (0.7mg) or intranasal placebo (sterile diluent) is administered. Study visits occur 1-3 weeks apart with intranasal glucagon or placebo applied in random order. Resting energy expenditure is measured via indirect calorimetry at baseline and over 90 minutes post-spray in 10-20 minute segments. Blood samples are taken at baseline and at regular intervals post-spray to measure glucagon, glucose and other hormones/metabolites. Appetite is assessed by visual analogue scale at 90 minutes post-spray followed by provision of a buffet-style meal for ad libitum food intake measurement.

Interventions

DRUGGlucagon

Intranasal glucagon

DRUGPlacebo

Intranasal placebo

Sponsors

University Health Network, Toronto
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)

Masking description

Single-blinded study with participant blinded to treatment

Intervention model description

Participants receive either glucagon or placebo as intranasal spray, in random order on 2 separate study visits, with indirect calorimetry, appetite and food intake assessment

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Body mass index 25- 40 kg/m2 * Hemoglobin in the normal range * Normal fasting glucose and HbA1C * Women of reproductive age should be on contraception (oral contraceptive pill or intra-uterine device/coil) for at least 1 month prior to and after the study.

Exclusion criteria

* Any history of heart disease or clinically significant, active, cardiovascular history * Study participant with active hepatic disease (except hepatic steatosis which is frequently seen in overweight/obese individuals) * Any current or previous history of biliary disease (including gall stones, biliary atresia and cholecystitis) or pancreatitis. * Any current or previous history of malignancy * Any significant active (over the past 12 months) disease of the gastrointestinal, pulmonary, neurological, renal (Cr \> 1.5 mg/dL) genitourinary, hematological systems, or has severe uncontrolled treated or untreated hyper/ hypotension (sitting diastolic BP \> 100 or systolic \> 180 or systolic BP\<100). * Allergy to any study medication * Pregnancy or breastfeeding

Design outcomes

Primary

MeasureTime frameDescription
Energy Expenditure90 minutesResting energy expenditure measured by indirect calorimetry

Secondary

MeasureTime frameDescription
Food intake90 minutesAd libitum food intake
Appetite90 minutesAppetite assessed by visual analogue scale ranging from 0 to 10 where 0 indicates no appetite and 10 indicates the highest appetite

Countries

Canada

Contacts

Primary ContactPriska Stahel, PhD
priska.stahel@uhn.ca416-581-7487
Backup ContactSatya Dash, MD
satya.dash@uhn.ca416-340-4800

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026