Clinical trial

The Role of the Amylin Analogue Cagrilintide in Bone Metabolism

Recruiting now · Phase 1 · 1 countries · Registry ID NCT07010432

Recruiting nowPhase 1Interventional

What this study is about

In this study we will investigate how the medicine cagrilintide affects bone health in women after menopause with obesity during weight loss, compared to treatment with placebo (the dummy medicine with no active substances) and semaglutide. The purpose is to examine whether cagrilintide can reduce the decline in bone mass associated to weight loss. Participants will either get cagrilintide, semaglutide, CagriSema (cagrilintide combined with semaglutide), or placebo. Which treatment participants get is decided by chance. Semaglutide is already approved for the treatment of overweight and obesity and can be prescribed by doctors. Cagrilintide and CagriSema are new medications currently under development for weight management. The study will last for about 79 weeks.

A promising-looking record is not the same as confirmed eligibility. The study team must review the full criteria and current recruitment status.

Basic eligibility

Age50 Years to 70 Years
SexFemale
Healthy volunteersNot accepted
ConditionObesity

Full registry criteria

Inclusion criteria * Female. * Post-menopausal at screening (defined as minimum 12 months of amenorrhea, high levels of follicular stimulating hormone (FSH) 16 - 130 international units per liter (IU/L), and low levels of anti-müllerian hormone (AMH) and inhibin B). * Age 50-70 years (both inclusive) at the time of signing the informed consent. * Body Mass Index (BMI) greater than or equal to \>= 30.0 kilograms per square meter (kg/m\^2). Exclusion criteria * Previous or current bone disease (e.g., osteoporosis, Paget's disease of bone, or bone cancer). * Presence of disease affecting bone metabolism (e.g., diabetes mellitus, hyperparathyroidism, hyper or hypothyroidism, chronic kidney disease, celiac disease, or inflammatory diseases (e.g., psoriatic arthritis or ankylosing spondylitis)). * Treatment with any medication affecting bone metabolism within 6 months prior to screening as judged by the investigator (e.g., anti-resorptive medication, anabolic medication, systemic hormone replacement therapy (HRT), or systemic corticosteroids).

Treatments and study arms

Cagrilintide

Drug

Participants will receive once-weekly cagrilintide subcutaneously.

Semaglutide

Drug

Participants will receive once-weekly semaglutide subcutaneously.

Placebo cagrilintide

Drug

Participants will receive once-weekly placebo matched to cagrilintide subcutaneously.

Placebo semaglutide

Drug

Participants will receive once-weekly placebo matched to semaglutide subcutaneously.

Primary outcomes

Relative change in volumetric bone mineral density (vBMD) of the total hip assessed by quantitative computed tomography (QCT)From baseline to end of treatment (week 68)

Measured in percentage (%).

Study locations

1 locations were listed when this page was built. The first 40 are shown.

Steno Diabetes Center Copenhagen🇩🇰 Herlev, Denmark