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Migergot (ERGOTAMINE)

FDA-approved withdrawn Small molecule Quality 55/100

Migergot (Ergotamine) is a small molecule ergot derivative that targets the 5-hydroxytryptamine receptor 1A. It was originally developed and is currently owned by various companies. FDA approved in 1948, it is used to treat cluster headache prevention, cluster headache syndrome, migraine, and vascular headache. As an off-patent medication, it is available from multiple generic manufacturers. Key safety considerations include its low bioavailability and short half-life.

At a glance

Generic nameERGOTAMINE
Drug classCentral Nervous System Stimulant [EPC]
Target5-hydroxytryptamine receptor 1A
ModalitySmall molecule
Therapeutic areaNeuroscience
PhaseFDA-approved
First approval1948

Approved indications

Boxed warnings

Common side effects

Drug interactions

Key clinical trials

Primary sources

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