Investigating the Acute Effects of Increasing Glucagon Exposure in Healthy Participants
Launched by NICOLAI JACOB WEWER ALBRECHTSEN · Apr 3, 2025
Trial Information
Current as of July 22, 2025
Not yet recruiting
Keywords
ClinConnect Summary
This clinical trial is looking at how increasing levels of a hormone called glucagon affect the way our bodies process sugar. Glucagon plays a key role in controlling blood sugar levels, and researchers want to see how its infusion impacts healthy individuals. Participants will take part in a single study day where they will have some initial blood tests, followed by a three-hour infusion of glucagon that will be gradually increased during the session.
To join this study, participants need to be between 25 and 70 years old and have a healthy body weight (a Body Mass Index of 25 or less). They should not have diabetes, be pregnant or breastfeeding, or have certain health conditions like liver or kidney disease. Throughout the study, participants can expect to provide blood samples to help researchers gather information on how glucagon affects their metabolism. It's important to note that this trial is not yet recruiting participants, so those interested will need to wait until it begins.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Capable of understanding the participant information and signing the consent form
- • Between 25 and 70 years of age at the time of screening
- • Body mass index (BMI) ≤ 25 kg/m2 at the time of screening
- Exclusion Criteria:
- • Enrolment in other research projects that might interfere with the study
- • Diabetes diagnosis (type 1 and 2)
- • Pregnancy or breastfeeding
- • Use of medications which, in the opinion of the investigator, may jeopardise participant's safety or compliance with the protocol
- • Impaired liver function defined as either alanine aminotransferase (ALAT) and/or aspartate aminotransferase (ASAT) ≥ 2 times normal values
- • Kidney disease defined as serum creatinine levels ≥ 126 μmol/L for male and ≥ 111 μmol/L for female
- • Inadequately treated blood pressure at screening defined as repeated resting blood pressure outside the range 90-150 mmHg for systolic and 50-100 mmHg for diastolic
- • Active or recent malignant disease
- • Current or history of severe alcohol use or drug/chemical abuse as per investigator's judgement
- • Any chronic disorders or severe diseases which, in the opinion of the investigator, might jeopardise participant's safety or compliance with the protocol
About Nicolai Jacob Wewer Albrechtsen
Nicolai Jacob Wewer Albrechtsen is a dedicated clinical trial sponsor with a strong focus on advancing medical research and innovative therapies. With a commitment to enhancing patient outcomes, he oversees the design, implementation, and management of clinical studies across various therapeutic areas. Leveraging a robust network of healthcare professionals and research institutions, Albrechtsen ensures compliance with regulatory standards while prioritizing ethical practices and patient safety. His expertise in clinical trial strategy and operations positions him as a key contributor to the development of groundbreaking treatments that address unmet medical needs.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Patients applied
Trial Officials
Nicolai J Wewer Albrecthsen, MD PhD
Principal Investigator
Department of Clinical Biochemistry, Copenhagen University Hospital - Bispebjerg and Frederiksberg Hospital, Copenhagen, Denmark
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported