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Zanaflex®

Icahn School of Medicine at Mount Sinai · FDA-approved active Small molecule

Zanaflex is an alpha-2 adrenergic agonist that reduces muscle spasticity by increasing inhibitory neurotransmission in the spinal cord.

Zanaflex is an alpha-2 adrenergic agonist that reduces muscle spasticity by increasing inhibitory neurotransmission in the spinal cord. Used for Spasticity associated with multiple sclerosis, Spasticity associated with spinal cord injury, Spasticity from other causes (e.g., stroke, cerebral palsy, traumatic brain injury).

At a glance

Generic nameZanaflex®
SponsorIcahn School of Medicine at Mount Sinai
Drug classAlpha-2 adrenergic agonist
TargetAlpha-2A adrenergic receptor
ModalitySmall molecule
Therapeutic areaNeurology
PhaseFDA-approved

Mechanism of action

Zanaflex (tizanidine) works by stimulating alpha-2 adrenergic receptors in the central nervous system, particularly in the spinal cord. This activation enhances the release of inhibitory neurotransmitters and reduces the release of excitatory amino acids, leading to decreased muscle tone and relief of spasticity. The drug is selective for alpha-2A receptors, which mediate its antispastic effects.

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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