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Frovatriptan


Mechanism of action:

Frovatriptan is a selective serotonin 5-HT₁B/5-HT₁D receptor agonist. Frovatriptan activates 5-HT₁B receptors on intracranial vascular smooth muscle, causing constriction of meningeal and intracranial blood vessels and reducing vascular pain signaling. It also activates 5-HT₁D receptors located on trigeminal nerve endings, inhibiting the release of pro-inflammatory and pain-related neuropeptides such as substance P and neurokinin A, thereby reducing neurogenic inflammation and pain transmission.

Reference(s):

1. Markus F et al. (2007). Frovatriptan review. Expert Opin Pharmacother. 


2. Easthope SE et al. (2001). Frovatriptan. CNS Drugs. 


3. Balbisi EA et al. (2006). Frovatriptan: a review of pharmacology, pharmacokinetics and clinical potential in the treatment of menstrual migraine. Ther Clin Risk Manag.

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