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Journavx (SUZETRIGINE)

Vertex Pharms Inc · FDA-approved active Small molecule Quality 65/100

Journavx blocks sodium channels in the nervous system to reduce pain signal transmission.

Journavx (suzetrigine) is a small molecule sodium channel blocker developed by Vertex Pharmaceuticals Inc. It is approved by the FDA for the treatment of moderate to severe acute pain and postoperative pain. Journavx works by blocking sodium channels in the nervous system, which helps to reduce the transmission of pain signals to the brain. It is a patented medication with no generic manufacturers available. As a relatively new medication, key safety considerations include its potential effects on the cardiovascular system and the need for further long-term studies.

At a glance

Generic nameSUZETRIGINE
SponsorVertex Pharms Inc
Drug classSodium Channel Blocker [EPC]
ModalitySmall molecule
Therapeutic areaMetabolic
PhaseFDA-approved
First approval2025

Mechanism of action

Suzetrigine is a selective blocker of the Na V 1.8 voltage-gated sodium channel, compared to other known voltage-gated sodium channels (Na V 1.1 through 1.9). Na V 1.8 is expressed in peripheral sensory neurons including dorsal root ganglion neurons, where its role is to transmit pain signals (action potentials). By selectively inhibiting Na V 1.8 channels, suzetrigine inhibits transmission of pain signals to the spinal cord and brain. M6-SUZ, a major active metabolite, is a less potent inhibitor of Na V 1.8 than suzetrigine by 3.7-fold.

Approved indications

Common side effects

Drug interactions

Key clinical trials

Patents

PatentExpiryType

Primary sources

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

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