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Cozaar (LOSARTAN POTASSIUM)

Merck & Co. · FDA-approved approved Small molecule Under review Quality 69/100

Cozaar (generic name: LOSARTAN POTASSIUM) is a Angiotensin 2 Receptor Blocker Small molecule drug developed by Merck & Co.. It is currently FDA-approved (first approved 1995) for Diabetic renal disease, Hypertension with Left Ventricular Hypertrophy, Hypertensive disorder.

Cozaar works by blocking the action of angiotensin II on its receptor, which helps to relax blood vessels and lower blood pressure.

Cozaar, also known as losartan, is used to prevent cardiovascular disease and has been studied for its potential to prevent paclitaxel-induced peripheral neuropathy in breast cancer patients. It has also been studied for its effects on conditions such as chronic kidney disease, rheumatoid arthritis, and diabetes mellitus.

At a glance

Generic nameLOSARTAN POTASSIUM
SponsorMerck & Co.
Drug classAngiotensin 2 Receptor Blocker
TargetType-1 angiotensin II receptor
ModalitySmall molecule
Therapeutic areaMetabolic
PhaseFDA-approved
First approval1995

Mechanism of action

Mechanism of ActionAngiotensin II [formed from angiotensin in reaction catalyzed by angiotensin converting enzyme (ACE, kininase II)], is potent vasoconstrictor, the primary vasoactive hormone of the renin-angiotensin system and an important component in the pathophysiology of hypertension. It also stimulates aldosterone secretion by the adrenal cortex. Losartan and its principal active metabolite block the vasoconstrictor and aldosterone-secreting effects of angiotensin II by selectively blocking the binding of angiotensin II to the AT1 receptor found in many tissues (e.g., vascular smooth muscle, adrenal gland). There is also an AT2 receptor found in many tissues but it is not known to be associated with cardiovascular homeostasis. Both losartan and its principal active metabolite do not exhibit any partial agonist activity at the AT1 receptor and have much greater affinity (about 1000-fold) for the AT1 receptor than for the AT2 receptor. In vitro binding studies indicate that losart

Approved indications

Boxed warnings

Common side effects

Drug interactions

Key clinical trials

Patents

PatentExpiryType
121568692041-10-07Formulation
118902732041-10-07Formulation

Primary sources

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

SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results
FDA Orange BookPatents + exclusivity

Competitive intelligence

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Frequently asked questions about Cozaar

What is Cozaar?

Cozaar (LOSARTAN POTASSIUM) is a Angiotensin 2 Receptor Blocker drug developed by Merck & Co., indicated for Diabetic renal disease, Hypertension with Left Ventricular Hypertrophy, Hypertensive disorder.

How does Cozaar work?

Cozaar works by blocking the action of angiotensin II on its receptor, which helps to relax blood vessels and lower blood pressure.

What is Cozaar used for?

Cozaar is indicated for Diabetic renal disease, Hypertension with Left Ventricular Hypertrophy, Hypertensive disorder, Hypertensive urgency.

Who makes Cozaar?

Cozaar is developed and marketed by Merck & Co. (see full Merck & Co. pipeline at /company/merck).

What is the generic name of Cozaar?

LOSARTAN POTASSIUM is the generic (nonproprietary) name of Cozaar.

What drug class is Cozaar in?

Cozaar belongs to the Angiotensin 2 Receptor Blocker class. See all Angiotensin 2 Receptor Blocker drugs at /class/angiotensin-2-receptor-blocker.

When was Cozaar approved?

Cozaar was first approved on 1995.

What development phase is Cozaar in?

Cozaar is FDA-approved (marketed).

What are the side effects of Cozaar?

Common side effects of Cozaar include Pemphigus, Synovitis, Hand deformity, Systemic lupus erythematosus, Contraindicated product administered, Maternal exposure during pregnancy.

What does Cozaar target?

Cozaar targets Type-1 angiotensin II receptor and is a Angiotensin 2 Receptor Blocker.

Related

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