Repatha

Drug

Drug Profile

Repatha (evolocumab) is a monoclonal antibody lipid-lowering therapy used to reduce LDL-C and cardiovascular risk in patients with established cardiovascular disease and familial hypercholesterolemia populations. The label describes it as targeting PCSK9 to increase LDL receptor availability and LDL clearance. U.S. approval was first granted in 2015.

Drug Class
PCSK9 inhibitor monoclonal antibody
Approval Status
FDA approved (Initial U.S. Approval: 2015)
Mechanism of Action
Inhibits binding of PCSK9 to LDL receptors, increasing LDL receptor recycling and LDL clearance from blood.
Brand Names
  • REPATHA
Indications
  • \Reduce risk of major adverse cardiovascular events in adults with established cardiovascular disease\
  • \Adjunct to diet for adults with primary hyperlipidemia including HeFH to reduce LDL-C\
  • \Adjunct to diet and other LDL-C-lowering therapies in pediatric patients >=10 years with HeFH\
  • \Adjunct to other LDL-C-lowering therapies in adults and pediatric patients >=10 years with HoFH\

Related News

Drugmakers Delay European Launches Amid US Pricing Pressure Under Trump

Pharmaceutical companies are delaying European drug launches due to uncertainty over U.S. pricing policies under President Trump. New drug launches in EU markets fell 35% following Trump's executive order on international reference pricing. Companies fear lower European prices could undermine their ability to maintain higher prices in the $700 billion U.S. market.

Related Clinical Trials

NCT ID Title Status Phase
NCT04573777

Reducing Intracranial atheroSclErosis With Repatha

TERMINATED PHASE4