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Setmelanotide

Generic Name
Setmelanotide
Brand Names
Imcivree
Drug Type
Small Molecule
Chemical Formula
C49H68N18O9S2
CAS Number
920014-72-8
Unique Ingredient Identifier
N7T15V1FUY
Background

Setmelanotide is the first available treatment for patients with pro-opiomelanocortin, proprotein subilisin/kexin type 1, or leptin deficiencies. It is an agonist of the melanocortin 4 receptor. Earlier attempts at agonizing MC4R (such as LY2112688) lead to successful weight loss, but also an increase in blood pressure and heart rate. Other earlier treatments for these patients included gastric bypass surgery. Patients taking setmelanotide experienced an average weight loss of 0.6 kg/week.

Imcivree was granted EMA orphan designation on November 19, 2018 and FDA approval on November 25, 2020. On May 4, 2023, it was approved by Health Canada.

Indication

Setmelanotide is indicated for chronic weight management in patients 6 years and older with obesity due to pro-opiomelanocortin (POMC) deficiency, proprotein subtilisin/kexin type 1 (PCSK1) deficiency, or leptin receptor (LEPR) deficiency as determined by an approved test demonstrating variants in POMC, PCSK1, or LEPR genes that are interpreted as pathogenic, likely pathogenic, or of uncertain significance. These conditions affect the MC4R signalling pathway.

Setmelanotide is also indicated for chronic weight management in patients 6 years and older with obesity due to Bardet-Biedl syndrome.

The drug is not reported to be effective in patients with POMC, PCSK1, or LEPR variants classified as benign or likely benign, as well as other types of obesity not listed above.

Associated Conditions
Leptin Receptor Deficiency Obesity, Obesity, Pro-opiomelanocortin (POMC) Deficiency Obesity, Proprotein convertase subtilisin/kexin type 1 (PCSK1) deficiency obesity
Associated Therapies
Chronic Weight Management therapy
globenewswire.com
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Rhythm Pharmaceuticals Announces FDA Acceptance for Expanding IMCIVREE® Use in Treating Pediatric Obesity

Rhythm Pharmaceuticals seeks FDA approval to expand IMCIVREE® (setmelanotide) use for treating obesity in children as young as 2 with Bardet-Biedl syndrome or POMC/LEPR deficiency, with a PDUFA goal date of December 26, 2024. The sNDA is based on Phase 3 trial data showing efficacy in reducing BMI in young children.
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