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ultra-micronized palmitoylethanolamide

Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico · FDA-approved active Small molecule

Ultra-micronized palmitoylethanolamide (um-PEA) is an endogenous lipid mediator that modulates inflammatory and neuropathic pain pathways through PPAR-α activation and mast cell stabilization.

Ultra-micronized palmitoylethanolamide (um-PEA) is an endogenous lipid mediator that modulates inflammatory and neuropathic pain pathways through PPAR-α activation and mast cell stabilization. Used for Neuropathic pain, Chronic pain conditions, Neuroinflammatory disorders.

At a glance

Generic nameultra-micronized palmitoylethanolamide
Also known asum-PEA, Normast
SponsorFondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
Drug classEndocannabinoid-like lipid mediator / PPAR-α agonist
TargetPPAR-α; mast cell stabilization
ModalitySmall molecule
Therapeutic areaNeurology / Pain Management / Immunology
PhaseFDA-approved

Mechanism of action

Palmitoylethanolamide is an endocannabinoid-like compound that reduces neuroinflammation by activating peroxisome proliferator-activated receptor alpha (PPAR-α) and stabilizing mast cells, thereby decreasing the release of pro-inflammatory mediators. The ultra-micronized formulation enhances bioavailability and absorption compared to standard formulations. This mechanism makes it effective for neuropathic pain and inflammatory conditions.

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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