Type 2 Diabetes (T2D) Clinical Trials

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Effect of CagriSema, Semaglutide and Cagrilintide on Skeletal Muscle Insulin Sensitivity, Composition and Function

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

The purpose of this clinical study is to look into how study medicines CagriSema (cagrilintide and semaglutide), cagrilintide, and semaglutide affects muscle health in people with excess body weight and slightly higher than normal blood sugar as they lose weight. Participants will either get CagriSema (a new study drug), cagrilintide (a new study drug), semaglutide (a drug that doctors can already prescribe to treat people with type 2 diabetes and excess body weight) or placebo (a placebo looks like the treatment being tested but doesn't have any active ingredients in it). Which treatment participants will get is decided by chance. Participants will be in this clinical study up to 15 months.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 50
Maximum Age: 70
Healthy Volunteers: f
View:

• Male or female.

• Age 50-70 years (both inclusive) at the time of signing the informed consent.

• Body Mass index (BMI) between 30.0 kilograms per square meter (kg/m\^2) and 39.9 kg/m\^2 (both inclusive) at screening (V1).

• Excess body weight should be due to excess adipose tissue, as judged by the investigator.

• Participant has a wish to lose at least 25 percentage (%) of body weight within 52 weeks of treatment.

Locations
Other Locations
Denmark
Aarhus Universitetshospital, Steno Diabetes Center Aarhus
RECRUITING
Aarhus N
Contact Information
Primary
Novo Nordisk
clinicaltrials@novonordisk.com
(+1) 866-867-7178
Time Frame
Start Date: 2026-04-10
Estimated Completion Date: 2028-06-09
Participants
Target number of participants: 100
Treatments
Experimental: CagriSema
Participants will receive once weekly subcutaneous (s.c.) dose of CagriSema (cagrilintide and semaglutide) for up to 52 weeks.
Experimental: Semaglutide
Participants will receive once weekly s.c. dose of semaglutide for up to 52 weeks.
Experimental: Cagrilintide
Participants will receive once weekly s.c. dose of cagrilintide for up to 52 weeks.
Placebo_comparator: Placebo
Participants will receive once weekly s.c. dose of placebo matched to cagrilintide/semaglutide for up to 52 weeks.
Related Therapeutic Areas
Sponsors
Leads: Novo Nordisk A/S

This content was sourced from clinicaltrials.gov