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Regadenoson myocardial perfusion imaging

University of Colorado, Denver · FDA-approved active Small molecule

Regadenoson myocardial perfusion imaging is a Adenosine A2A receptor agonist Small molecule drug developed by University of Colorado, Denver. It is currently FDA-approved for Myocardial perfusion imaging in patients unable to exercise or requiring pharmacologic stress testing. Also known as: Cardiolite (sestamibi), Regadenoson (Lexiscan).

Regadenoson is a selective adenosine A2A receptor agonist that increases coronary blood flow to detect areas of reduced perfusion during cardiac imaging.

Regadenoson is a selective adenosine A2A receptor agonist that increases coronary blood flow to detect areas of reduced perfusion during cardiac imaging. Used for Myocardial perfusion imaging in patients unable to exercise or requiring pharmacologic stress testing.

At a glance

Generic nameRegadenoson myocardial perfusion imaging
Also known asCardiolite (sestamibi), Regadenoson (Lexiscan)
SponsorUniversity of Colorado, Denver
Drug classAdenosine A2A receptor agonist
TargetAdenosine A2A receptor
ModalitySmall molecule
Therapeutic areaCardiovascular
PhaseFDA-approved

Mechanism of action

Regadenoson binds to adenosine A2A receptors on coronary vascular smooth muscle, causing vasodilation and increasing blood flow preferentially to normally perfused myocardium. This creates a differential in blood flow between healthy and ischemic regions, allowing visualization of perfusion defects on imaging. It is used as a pharmacologic stress agent as an alternative to exercise stress testing in myocardial perfusion imaging studies.

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 Regadenoson myocardial perfusion imaging

What is Regadenoson myocardial perfusion imaging?

Regadenoson myocardial perfusion imaging is a Adenosine A2A receptor agonist drug developed by University of Colorado, Denver, indicated for Myocardial perfusion imaging in patients unable to exercise or requiring pharmacologic stress testing.

How does Regadenoson myocardial perfusion imaging work?

Regadenoson is a selective adenosine A2A receptor agonist that increases coronary blood flow to detect areas of reduced perfusion during cardiac imaging.

What is Regadenoson myocardial perfusion imaging used for?

Regadenoson myocardial perfusion imaging is indicated for Myocardial perfusion imaging in patients unable to exercise or requiring pharmacologic stress testing.

Who makes Regadenoson myocardial perfusion imaging?

Regadenoson myocardial perfusion imaging is developed and marketed by University of Colorado, Denver (see full University of Colorado, Denver pipeline at /company/university-of-colorado-denver).

Is Regadenoson myocardial perfusion imaging also known as anything else?

Regadenoson myocardial perfusion imaging is also known as Cardiolite (sestamibi), Regadenoson (Lexiscan).

What drug class is Regadenoson myocardial perfusion imaging in?

Regadenoson myocardial perfusion imaging belongs to the Adenosine A2A receptor agonist class. See all Adenosine A2A receptor agonist drugs at /class/adenosine-a2a-receptor-agonist.

What development phase is Regadenoson myocardial perfusion imaging in?

Regadenoson myocardial perfusion imaging is FDA-approved (marketed).

What are the side effects of Regadenoson myocardial perfusion imaging?

Common side effects of Regadenoson myocardial perfusion imaging include Dyspnea, Chest discomfort, Headache, Flushing, Palpitations, Dizziness.

What does Regadenoson myocardial perfusion imaging target?

Regadenoson myocardial perfusion imaging targets Adenosine A2A receptor and is a Adenosine A2A receptor agonist.

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