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Aramchol free acid

Galmed Pharmaceuticals Ltd · Phase 3 active Small molecule

Aramchol inhibits stearoyl-CoA desaturase 1 (SCD1), an enzyme that converts saturated fatty acids to monounsaturated fatty acids, thereby reducing hepatic lipogenesis and improving liver metabolism.

Aramchol inhibits stearoyl-CoA desaturase 1 (SCD1), an enzyme that converts saturated fatty acids to monounsaturated fatty acids, thereby reducing hepatic lipogenesis and improving liver metabolism. Used for Non-alcoholic steatohepatitis (NASH), Non-alcoholic fatty liver disease (NAFLD).

At a glance

Generic nameAramchol free acid
Also known as3β-arachidylamido-7α,12α-dihydroxy-5β-cholan-24-oic acid, Two tablets of Aramchol free acid
SponsorGalmed Pharmaceuticals Ltd
Drug classSCD1 inhibitor
TargetStearoyl-CoA desaturase 1 (SCD1)
ModalitySmall molecule
Therapeutic areaHepatology
PhasePhase 3

Mechanism of action

By blocking SCD1, aramchol decreases the production of monounsaturated fatty acids in the liver, which reduces hepatic steatosis and improves insulin sensitivity. This mechanism addresses the underlying metabolic dysfunction in non-alcoholic fatty liver disease (NAFLD) and non-alcoholic steatohepatitis (NASH), reducing liver fat accumulation and inflammation.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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