Development of Cagrilintide, a Long-Acting Amylin Analogue.
Thomas KruseJakob Lerche HansenKirsten DahlLauge SchäfferUlrich SensfussChristian PoulsenMorten SchleinAnn Maria Kruse HansenClaus Bekker JeppesenCharlotta Dornonville de la CourTrine Ryberg ClausenEva JohanssonSimone FulleRikke Bjerring SkyggebjergKirsten RaunPublished in: Journal of medicinal chemistry (2021)
A hallmark of the pancreatic hormone amylin is its high propensity toward the formation of amyloid fibrils, which makes it a challenging drug design effort. The amylin analogue pramlintide is commercially available for diabetes treatment as an adjunct to insulin therapy but requires three daily injections due to its short half-life. We report here the development of the stable, lipidated long-acting amylin analogue cagrilintide (23) and some of the structure-activity efforts that led to the selection of this analogue for clinical development with obesity as an indication. Cagrilintide is currently in clinical trial and has induced significant weight loss when dosed alone or in combination with the GLP-1 analogue semaglutide.
Keyphrases
- weight loss
- type diabetes
- clinical trial
- metabolic syndrome
- cardiovascular disease
- glycemic control
- emergency department
- bariatric surgery
- physical activity
- randomized controlled trial
- body mass index
- oxidative stress
- drug induced
- gastric bypass
- open label
- study protocol
- ultrasound guided
- platelet rich plasma
- high fat diet induced
- phase ii
- phase iii
- double blind