Lipid Tracker

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

Approved

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

Approved

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

Approved

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)

Approved

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)

Approved

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)

Approved

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)

Approved

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)

Approved

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

Phase 3

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 listing

Olpasiran

Phase 3

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 listing

Lepodisiran

Phase 3

siRNA targeting lipoprotein(a) production

ACCLAIM-Lp(a) outcomes trial, ~16,700 patients, currently enrolling. Not yet FDA-approved.

Sponsor: Eli Lilly

Trial listing

Muvalaplin

Phase 3

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 listing

Zerlasiran

Phase 2 completed, Phase 3 planning

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