Current & upcoming therapies
Approved options first, since that's what most people need right now. Pipeline drugs are below — none of them are available yet.
Approved today
Atorvastatin
Statin (HMG-CoA reductase inhibitor)
High-intensity statin, first-line therapy for most people with elevated LDL. Generic, widely available. TNT showed intensive atorvastatin dosing reduced major cardiovascular events versus lower-dose therapy.
Trial details
Key trial: TNT (Treating to New Targets) — read the source
Rosuvastatin
Statin (HMG-CoA reductase inhibitor)
High-intensity statin, generic. JUPITER showed rosuvastatin reduced cardiovascular events in people with normal LDL but elevated CRP, broadening who statins are considered for.
Trial details
Key trial: JUPITER — read the source
Ezetimibe
Cholesterol absorption inhibitor
Usually added to a statin when LDL goals aren't met on statin alone. IMPROVE-IT showed adding ezetimibe to statin therapy further reduced cardiovascular events after acute coronary syndrome.
Trial details
Key trial: IMPROVE-IT — read the source
Evolocumab (Repatha)
PCSK9 inhibitor (monoclonal antibody)
Injectable, typically every 2-4 weeks. Approved 2015. FOURIER showed evolocumab added to statin therapy further reduced cardiovascular events in people with established ASCVD.
Trial details
Key trial: FOURIER — read the source
Alirocumab (Praluent)
PCSK9 inhibitor (monoclonal antibody)
Injectable, typically every 2-4 weeks. Approved 2015. ODYSSEY OUTCOMES showed alirocumab reduced cardiovascular events after a recent acute coronary syndrome.
Trial details
Key trial: ODYSSEY OUTCOMES — read the source
Inclisiran (Leqvio)
siRNA (blocks PCSK9 production in the liver)
Injectable, only twice a year after the first two starter doses. Approved 2021. ORION trials showed sustained LDL reduction with infrequent dosing versus the every-2-4-week PCSK9 antibodies.
Trial details
Key trial: ORION-10 / ORION-11 — read the source
Bempedoic acid (Nexletol)
ATP-citrate lyase (ACL) inhibitor
Oral, once-daily pill, often used for statin-intolerant patients since it's not associated with the muscle-related side effects statins can cause. Approved 2020. CLEAR Outcomes showed reduced cardiovascular events in statin-intolerant patients.
Trial details
Key trial: CLEAR Outcomes — read the source
Lerodalcibep (Lerochol)
PCSK9 inhibitor (third-generation, small recombinant fusion protein)
Once-monthly, self-administered injection, room-temperature stable for up to 3 months (most PCSK9 injectables need refrigeration). FDA-approved December 2025 for hypercholesterolemia including heterozygous FH, launched in the US in spring 2026 as a prefilled syringe, with an autoinjector following later in the year. A direct-to-patient cash program is available at $199/month.
Trial details
Key trial: LIBerate program — read the source
In development, not yet approved
Obicetrapib
CETP inhibitor, raises HDL and lowers LDL
PREVAIL outcomes trial: interim analysis 4Q2026, results expected 1Q2027. Positive CHMP opinion in Europe (July 2026), EU decision pending. Not yet FDA-approved.
Sponsor: NewAmsterdam Pharma
Trial listingOlpasiran
siRNA targeting lipoprotein(a) production
OCEAN(a)-Outcomes trial, ~7,000 patients with established ASCVD and high Lp(a), estimated completion December 2026. Not yet FDA-approved.
Sponsor: Amgen
Trial listingLepodisiran
siRNA targeting lipoprotein(a) production
ACCLAIM-Lp(a) outcomes trial, ~16,700 patients, currently enrolling. Not yet FDA-approved.
Sponsor: Eli Lilly
Trial listingMuvalaplin
Oral small molecule, blocks lipoprotein(a) particle assembly
MOVE-Lp(a) outcomes trial, ~10,450 patients, began enrolling late 2025, primary completion estimated 2031. First oral option in this class. Not yet FDA-approved.
Sponsor: Eli Lilly
Trial listingZerlasiran
siRNA targeting lipoprotein(a) production
Phase 2 (JAMA 2024) showed strong Lp(a) reduction. Phase 3 program not yet underway. Not yet FDA-approved.
Sponsor: Silence Therapeutics
Trial listing