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Amlodipine + Simvastatin

University of Pavia · FDA-approved active Small molecule

Amlodipine + Simvastatin is a Calcium channel blocker + HMG-CoA reductase inhibitor (statin) Small molecule drug developed by University of Pavia. It is currently FDA-approved for Hypertension with hypercholesterolemia, Cardiovascular risk reduction in patients requiring both antihypertensive and lipid-lowering therapy.

This combination reduces blood pressure by blocking calcium channels in vascular smooth muscle (amlodipine) and lowers cholesterol by inhibiting HMG-CoA reductase (simvastatin).

This combination reduces blood pressure by blocking calcium channels in vascular smooth muscle (amlodipine) and lowers cholesterol by inhibiting HMG-CoA reductase (simvastatin). Used for Hypertension with hypercholesterolemia, Cardiovascular risk reduction in patients requiring both antihypertensive and lipid-lowering therapy.

At a glance

Generic nameAmlodipine + Simvastatin
SponsorUniversity of Pavia
Drug classCalcium channel blocker + HMG-CoA reductase inhibitor (statin)
TargetL-type voltage-gated calcium channel; HMG-CoA reductase
ModalitySmall molecule
Therapeutic areaCardiovascular
PhaseFDA-approved

Mechanism of action

Amlodipine is a dihydropyridine calcium channel blocker that prevents calcium influx into vascular smooth muscle cells, causing vasodilation and reduced peripheral resistance. Simvastatin is a statin that competitively inhibits HMG-CoA reductase, the rate-limiting enzyme in cholesterol synthesis, thereby reducing LDL cholesterol and triglycerides. Together, they address two major cardiovascular risk factors.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

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

Competitive intelligence

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Frequently asked questions about Amlodipine + Simvastatin

What is Amlodipine + Simvastatin?

Amlodipine + Simvastatin is a Calcium channel blocker + HMG-CoA reductase inhibitor (statin) drug developed by University of Pavia, indicated for Hypertension with hypercholesterolemia, Cardiovascular risk reduction in patients requiring both antihypertensive and lipid-lowering therapy.

How does Amlodipine + Simvastatin work?

This combination reduces blood pressure by blocking calcium channels in vascular smooth muscle (amlodipine) and lowers cholesterol by inhibiting HMG-CoA reductase (simvastatin).

What is Amlodipine + Simvastatin used for?

Amlodipine + Simvastatin is indicated for Hypertension with hypercholesterolemia, Cardiovascular risk reduction in patients requiring both antihypertensive and lipid-lowering therapy.

Who makes Amlodipine + Simvastatin?

Amlodipine + Simvastatin is developed and marketed by University of Pavia (see full University of Pavia pipeline at /company/university-of-pavia).

What drug class is Amlodipine + Simvastatin in?

Amlodipine + Simvastatin belongs to the Calcium channel blocker + HMG-CoA reductase inhibitor (statin) class. See all Calcium channel blocker + HMG-CoA reductase inhibitor (statin) drugs at /class/calcium-channel-blocker-hmg-coa-reductase-inhibitor-statin.

What development phase is Amlodipine + Simvastatin in?

Amlodipine + Simvastatin is FDA-approved (marketed).

What are the side effects of Amlodipine + Simvastatin?

Common side effects of Amlodipine + Simvastatin include Headache, Peripheral edema, Flushing, Muscle pain/myalgia, Elevated liver enzymes, Dizziness.

What does Amlodipine + Simvastatin target?

Amlodipine + Simvastatin targets L-type voltage-gated calcium channel; HMG-CoA reductase and is a Calcium channel blocker + HMG-CoA reductase inhibitor (statin).

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing