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Rosuvastatin-ranitidine

Centre de Recherche de l'Institut Universitaire de Cardiologie et de Pneumologie de Quebec · FDA-approved active Small molecule Under review

Rosuvastatin-ranitidine is a Fixed-dose combination: HMG-CoA reductase inhibitor + H2-receptor antagonist Small molecule drug developed by Centre de Recherche de l'Institut Universitaire de Cardiologie et de Pneumologie de Quebec. It is currently FDA-approved for Hypercholesterolemia with gastrointestinal intolerance or risk.

This is a fixed-dose combination of rosuvastatin (a statin that lowers cholesterol) and ranitidine (an H2-receptor antagonist that reduces stomach acid).

Rosuvastatin is a statin used to treat coronary artery disease, and it is often combined with other medications. Ranitidine, a histamine H2 receptor antagonist, is a small molecule that works by blocking the histamine H2 receptor, which is involved in stomach acid production.

At a glance

Generic nameRosuvastatin-ranitidine
SponsorCentre de Recherche de l'Institut Universitaire de Cardiologie et de Pneumologie de Quebec
Drug classFixed-dose combination: HMG-CoA reductase inhibitor + H2-receptor antagonist
TargetHMG-CoA reductase (rosuvastatin component); Histamine H2 receptor (ranitidine component)
ModalitySmall molecule
Therapeutic areaCardiovascular
PhaseFDA-approved

Mechanism of action

Rosuvastatin inhibits HMG-CoA reductase to reduce LDL cholesterol and cardiovascular risk, while ranitidine blocks histamine H2 receptors on gastric parietal cells to reduce acid secretion. The combination is designed to provide cardiovascular protection while mitigating gastrointestinal side effects that may occur with statin monotherapy.

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

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Frequently asked questions about Rosuvastatin-ranitidine

What is Rosuvastatin-ranitidine?

Rosuvastatin-ranitidine is a Fixed-dose combination: HMG-CoA reductase inhibitor + H2-receptor antagonist drug developed by Centre de Recherche de l'Institut Universitaire de Cardiologie et de Pneumologie de Quebec, indicated for Hypercholesterolemia with gastrointestinal intolerance or risk.

How does Rosuvastatin-ranitidine work?

This is a fixed-dose combination of rosuvastatin (a statin that lowers cholesterol) and ranitidine (an H2-receptor antagonist that reduces stomach acid).

What is Rosuvastatin-ranitidine used for?

Rosuvastatin-ranitidine is indicated for Hypercholesterolemia with gastrointestinal intolerance or risk.

Who makes Rosuvastatin-ranitidine?

Rosuvastatin-ranitidine is developed and marketed by Centre de Recherche de l'Institut Universitaire de Cardiologie et de Pneumologie de Quebec (see full Centre de Recherche de l'Institut Universitaire de Cardiologie et de Pneumologie de Quebec pipeline at /company/centre-de-recherche-de-l-institut-universitaire-de-cardiologie-et-de-pneumologie).

What drug class is Rosuvastatin-ranitidine in?

Rosuvastatin-ranitidine belongs to the Fixed-dose combination: HMG-CoA reductase inhibitor + H2-receptor antagonist class. See all Fixed-dose combination: HMG-CoA reductase inhibitor + H2-receptor antagonist drugs at /class/fixed-dose-combination-hmg-coa-reductase-inhibitor-h2-receptor-antagonist.

What development phase is Rosuvastatin-ranitidine in?

Rosuvastatin-ranitidine is FDA-approved (marketed).

What are the side effects of Rosuvastatin-ranitidine?

Common side effects of Rosuvastatin-ranitidine include Headache, Myalgia, Gastrointestinal upset, Elevated liver enzymes.

What does Rosuvastatin-ranitidine target?

Rosuvastatin-ranitidine targets HMG-CoA reductase (rosuvastatin component); Histamine H2 receptor (ranitidine component) and is a Fixed-dose combination: HMG-CoA reductase inhibitor + H2-receptor antagonist.

Related

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