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Cabergoline (Dopamine Agonist)

University Hospital, Basel, Switzerland · FDA-approved active Small molecule

Cabergoline is a dopamine D2 receptor agonist that inhibits prolactin secretion from the anterior pituitary gland.

Cabergoline is a dopamine D2 receptor agonist that inhibits prolactin secretion from the anterior pituitary gland. Used for Hyperprolactinemia (prolactin-secreting pituitary adenomas and idiopathic hyperprolactinemia), Restless legs syndrome, Parkinson's disease (adjunctive therapy).

At a glance

Generic nameCabergoline (Dopamine Agonist)
SponsorUniversity Hospital, Basel, Switzerland
Drug classDopamine agonist
TargetDopamine D2 receptor
ModalitySmall molecule
Therapeutic areaEndocrinology
PhaseFDA-approved

Mechanism of action

Cabergoline binds to dopamine D2 receptors on lactotroph cells in the pituitary, mimicking dopamine's natural inhibitory effect on prolactin release. This leads to rapid and sustained suppression of elevated prolactin levels. It is highly selective for D2 receptors and has a long half-life, allowing for less frequent dosing compared to other dopamine agonists.

Approved indications

Common side effects

Key clinical trials

Primary sources

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

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