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Capsaicin 8%

Averitas Pharma, Inc. · FDA-approved active Small molecule

Capsaicin activates TRPV1 nociceptors on nerve fibers, causing initial stimulation followed by desensitization and depletion of substance P, resulting in reduced pain signaling.

Capsaicin activates TRPV1 nociceptors on nerve fibers, causing initial stimulation followed by desensitization and depletion of substance P, resulting in reduced pain signaling. Used for Neuropathic pain (postherpetic neuralgia, peripheral neuropathy), Localized musculoskeletal pain.

At a glance

Generic nameCapsaicin 8%
Also known asQutenza®, QUTENZA®, Qutenza
SponsorAveritas Pharma, Inc.
Drug classTopical analgesic; TRPV1 agonist
TargetTRPV1 (transient receptor potential vanilloid 1)
ModalitySmall molecule
Therapeutic areaPain Management
PhaseFDA-approved

Mechanism of action

Capsaicin is a natural alkaloid that binds to and activates the transient receptor potential vanilloid 1 (TRPV1) channel on C-fiber nociceptors. Acute activation causes a burning sensation, but with sustained exposure, the nerve fibers become desensitized and substance P (a key pain neurotransmitter) becomes depleted, leading to prolonged analgesia in the treated area. The 8% topical patch formulation delivers high local concentrations to provide sustained pain relief.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results