Drug intelligence / Profile preview

odevixibat + cholestyramine

Development stage
Unknown
Lead developer
Ipsen
Modality
Implantable Hydrogels → Hydrogel Systems → Drug Delivery Systems, Small Molecules, Non-biodegradable Polymers → Polymer-based Nanoparticles → Nanoparticles → Drug Delivery Systems, Biodegradable Polymers → Polymer-based Nanoparticles → Nanoparticles → Drug Delivery Systems, Injectable Hydrogels → Hydrogel Systems → Drug Delivery Systems
Administration
Oral
01

Overview

Odevixibat + cholestyramine is a combination of two agents affecting bile acid homeostasis, used for conditions involving cholestatic pruritus and lipid disorders. Odevixibat is a small molecule inhibitor of the ileal sodium/bile acid cotransporter (ASBT/IBAT), reducing bile acid reabsorption in the terminal ileum and lowering systemic bile acids, primarily indicated for pruritus in progressive familial intrahepatic cholestasis (PFIC)[1][5]. Cholestyramine is a bile acid sequestrant that binds bile acids in the gut, preventing their reabsorption and facilitating excretion, used for the management of hypercholesterolemia and pruritus associated with partial biliary obstruction[2][8]. Both drugs ultimately lower circulating bile acids, but by distinct mechanisms—odevixibat reduces absorption, while cholestyramine increases excretion. The clinical use of this combination is based on symptom control in conditions such as PFIC and cholestatic pruritus, although co-administration reduces odevixibat efficacy due to absorption interference[3][7].

Other names
cholestyramine resin
02

Targets

SLC10A2 (Solute carrier family 10 member 2)

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