Market access risk in cardiology
Cardiology is the field where the cheapest medicines on earth set the price of the newest. Statins, blood-pressure tablets and the older anticoagulants cost pennies, work well, and are taken by tens of millions of people — so every new cardiovascular drug is judged against them, on populations so large that even a modest price becomes a national budget line. At the same time the field now has its own rare corner: inherited cholesterol disorders, heart-muscle disease and amyloid heart disease, where a few thousand patients meet prices once reserved for cancer. This page brings together MARA's independent assessments of reimbursement risk across both ends of the field.
What payers ask in cardiology
Does it prevent events, or move a number? Most cardiovascular approvals rest on a laboratory value — cholesterol, blood pressure, triglycerides — long before anyone knows whether fewer heart attacks and strokes follow. Payers have learned to separate the two. A drug that only moves the number is reimbursed narrowly, or not at all, until the outcomes trial reads out.
How much better than a generic, and for whom? The comparator in cardiology is usually a tablet that costs almost nothing. Payers ask what the new drug adds on top of it, and then draw the reimbursed group as tightly as the evidence allows — the highest-risk patients, those who cannot tolerate the standard, those already on maximum therapy.
What does a lifetime on treatment cost the system? Cardiovascular drugs are taken for decades by very large populations. Payers multiply price by years by patients before they look at anything else, and the answer decides whether a drug is covered broadly, covered with prior authorisation, or placed behind cheaper steps.
Is the convenience worth paying for? Twice-yearly injections, once-daily tablets replacing injections, drugs that need no monitoring: the field increasingly sells adherence. Payers accept that patients take convenient medicines more faithfully — and still ask for proof that the convenience changes outcomes, not only prescriptions.
The MARA record in cardiology
Cardiology holds nearly thirty dated assessments in the MARA catalogue: cholesterol and triglyceride lowering from oral tablets to twice-yearly injections, resistant hypertension, anticoagulation and stroke prevention, heart failure, hypertrophic cardiomyopathy and amyloid heart disease. Each report answers the same payer questions, carries its "as of" date, and stays on the record — when the evidence moves, a newer vintage replaces the older one visibly, never silently. Assessments are produced on MARA's own initiative for awareness; the current MARA Rating for any drug is available on request.
Current assessments (24)
- LIPFENDRA / Enlicitide for treating primary hypercholesterolemia or mixed dyslipidemia as of August 2026
- Lerodalcibep for Hypercholesterolaemia as of August 2026
- Ubeslo / Obicetrapib for Primary Hypercholesterolaemia and Mixed Dyslipidaemia as of August 2026
- Tryngolza / Olezarsen for Severe Hypertriglyceridemia as of August 2026
- Tryngolza / olezarsen for familial Chylomicronemia Syndrome as of June 2026
- Baxfendy / baxdrostat for treating uncontrolled or resistant hypertension as of June 2026
- Etripamil for acute PSVT episode termination as of February 2026
- Abelacimab for thrombosis (e.g. atrial fibrillation-related stroke prevention and venous thromboembolism) as of January 2026
- Sotatercept for treatment of heart failure with preserved ejection fraction complicated by combined pulmonary hypertension as of November 2025
- Aficamten for treating symptomatic obstructive hypertrophic cardiomyopathy as of August 2025
- Evkeeza / evinacumab for treating homozygous familial hypercholesterolaemia in people 12 years and over as of September 2024
- Vyndaqel / tafamidis for treating transthyretin amyloidosis with cardiomyopathy as of June 2024
- Jardiance / empagliflozin for treating chronic heart failure with preserved or mildly reduced ejection fraction as of November 2023
- Mavacamten for treating symptomatic obstructive hypertrophic cardiomyopathy as of September 2023
- Dapagliflozin for treating chronic heart failure with preserved or mildly reduced ejection fraction as of June 2023
- Icosapent ethyl for reducing the risk of cardiovascular events in people with raised triglycerides as of July 2022
- Empagliflozin / jardiance for treating chronic heart failure with reduced ejection fraction as of March 2022
- Leqvio / inclisiran for treating primary hypercholesterolaemia or mixed dyslipidaemia as of October 2021
- Rivaroxaban for the prevention of stroke and systemic embolism in people with atrial fibrillation as of July 2021
- Edoxaban / lixiana for preventing stroke and systemic embolism in people with non-valvular atrial fibrillation as of July 2021
- Pradaxa / dabigatran etexilate for the prevention of stroke and systemic embolism in atrial fibrillation as of July 2021
- Apixaban / eliquis for preventing stroke and systemic embolism in people with non-valvular atrial fibrillation as of July 2021
- Nilemdo / bempedoic acid for treating primary hypercholesterolaemia or mixed dyslipidaemia as of April 2021
- Forxiga / dapagliflozin for treating chronic heart failure with reduced ejection fraction as of February 2021
Earlier assessments (each replaced by a newer version)
- Baxdrostat for treatment-Resistant Hypertension as of April 2026
- Lerochol / lerodalcibep-liga for lDL-C Reduction in adults with hypercholesterolemia, including HeFH as of February 2026
- Baxdrostat for treating uncontrolled and resistant hypertension as of September 2025
Selected commentary
- Aficamten in hypertrophic cardiomyopathy
- FDA approves AstraZeneca’s Baxfendy for hypertension
- Surveillance update: baxdrostat affirmed following the April 2026 review
For how a MARA Rating is built, see the methodology and what a MARA Rating is. To request the current rating for any drug in this area, use the contact form.