Volixibat

Generic Name
Volixibat
Brand Names
-
Drug Type
Small Molecule
Chemical Formula
C38H51N3O12S2
CAS Number
1025216-57-2
Unique Ingredient Identifier
X2JZ0451H8
Background

Volixibat, also known as SHP626 or LUM002, is an investigational drug that will potentially be used for the treatment of Non-Alcoholic Steatohepatitis (NASH). If approved for use, it will be the first available agent for the treatment of NASH.

Volixibat is a selective inhibitor of the apical sodium-dependent bile acid transporter (ASBT), a transmembrane protein primarily expressed by enterocytes of the ileum. Also known as the ileal bile acid transporter (IBAT), ASBT is primarily responsible for the enterohepatic recirculation of bile acids and ultimately for hepatic lipid and glucose metabolism . Inhibiting this enzyme results in a decrease of bile acids returning to the liver, which is helpful for the treatment of NASH as abnormal cholesterol metabolism and accumulation of free cholesterol in the liver have been implicated in its pathogenesis.

According to Shire, the pharmaceutical manufacturer of Volixibat, it has been granted fast track status by the Food and Drug Administration due to promising initial results and a need for therapeutic treatments for NASH.

Indication

Volixibat is an investigational drug that has not been approved for use in any conditions.

Associated Conditions
-
Associated Therapies
-
stocktitan.net
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Volixibat Granted Breakthrough Therapy Designation for Cholestatic Pruritus in ...

FDA grants Breakthrough Therapy Designation to volixibat for treating cholestatic pruritus in primary biliary cholangitis (PBC) patients, based on positive Phase 2b VANTAGE study results showing significant improvement in pruritus vs. placebo. Enrollment for the confirmatory portion of the study is expected to complete in 2026.
hcplive.com
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FDA Grants Breakthrough Therapy Designation to Volixibat for Cholestatic Pruritus in PBC

Mirum Pharmaceuticals' volixibat received Breakthrough Therapy Designation for treating cholestatic pruritus in primary biliary cholangitis (PBC) based on VANTAGE study results showing significant pruritus improvement. Volixibat, an oral IBAT inhibitor, aims to reduce bile acids and is being evaluated in phase 2b studies for PBC and primary sclerosing cholangitis.
prnewswire.com
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Ipsen's IQIRVO Approval Has Intensified the Primary Biliary Cholangitis Market Space

The European Commission approves Ipsen's IQIRVO (elafibranor) for primary biliary cholangitis, the first new therapy in the EU in a decade. Other companies, including CymaBay, Zydus, and GlaxoSmithKline, are preparing to enter the market. The approval is based on the Phase III ELATIVE trial, showing a 47% clinical benefit of IQIRVO combined with UDCA. Additionally, Gilead Sciences' LIVDELZI (seladelpar) received FDA accelerated approval for PBC.
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