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Capsaicine low dose 0.04 %

University Hospital, Clermont-Ferrand · FDA-approved active Small molecule

Capsaicin activates TRPV1 nociceptors on nerve fibers, causing initial stimulation followed by desensitization and reduced pain signal transmission.

Capsaicin activates TRPV1 nociceptors on nerve fibers, causing initial stimulation followed by desensitization and reduced pain signal transmission. Used for Neuropathic pain (localized), Postherpetic neuralgia, Musculoskeletal pain.

At a glance

Generic nameCapsaicine low dose 0.04 %
Also known ascontrol treatment
SponsorUniversity Hospital, Clermont-Ferrand
Drug classTopical analgesic; TRPV1 agonist
TargetTRPV1 (transient receptor potential vanilloid 1)
ModalitySmall molecule
Therapeutic areaPain management; Dermatology
PhaseFDA-approved

Mechanism of action

Capsaicin is a vanilloid compound that binds to and activates the transient receptor potential vanilloid 1 (TRPV1) channel on C-fiber nociceptors. Repeated or sustained exposure leads to desensitization of these pain-sensing neurons, reducing their ability to transmit pain signals. At low doses in topical formulations, this results in localized analgesia without systemic 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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