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Also: (−)-epigallocatechin-3-gallate · green tea catechins · Camellia sinensis
Four separate measurements, never averaged. Independent evidence counts only studies with no sponsor attached. Methodology version v2.0-2026-10 · how we grade evidence
Claimed to increase thermogenesis and fat oxidation, cause weight loss and reduce body fat, and act as an antioxidant and anti-cancer agent. The Cochrane review of 15 weight-loss and three weight-maintenance studies in 1,945 completing participants found, in the six studies conducted outside Japan, a mean difference of −0.04 kg (95% CI −0.5 to 0.4) — forty grams, not statistically significant. The eight Japanese studies were too dissimilar to pool and individually ranged from −0.2 kg to −3.5 kg. The geographic split is itself the finding: the only impressive numbers come from one country’s trials, which could not be combined with the rest.
There is a verified hepatotoxicity signal, demonstrated in randomised trials and acted on by two independent authorities. EFSA concluded that EGCG at or above 800 mg/day taken as a food supplement significantly raises serum transaminases relative to control, and explicitly did not set a safe supplement dose or an upper intake level — the strongest available statement that the safe margin is unknown. The USP review found the injury pattern is hepatocellular, that published case reports associate hepatotoxicity with EGCG intakes of about 140 mg up to roughly 1,000 mg/day with substantial, possibly genetic, individual variability, and that repeated bolus doses taken while fasting increase catechin bioavailability, probably by saturating first-pass elimination. It found no evidence that solvent residues, pesticide residues, pyrrolizidine alkaloids or elemental impurities were involved: the hepatotoxicity is attributable to the catechins themselves. Note that the 140 mg lower bound of reported case intakes sits far below the European Union’s 800 mg/day regulatory ceiling.
Catechins from traditionally prepared infusions, and reconstituted drinks of equivalent composition, were considered generally safe at reported intakes, with rare liver injury most likely idiosyncratic. Regulation of this compound now consists largely of warnings.
At a glance
EGCG inhibits catechol-O-methyltransferase, prolonging noradrenergic signalling and theoretically increasing thermogenesis and lipolysis, with synergy from the caffeine naturally present in extracts. This is not confirmed in humans as a route to fat loss. The Cochrane review found essentially no weight effect in non-Japanese trials, so whatever acute thermogenic effect exists does not translate into clinically meaningful fat loss.
Dated determinations, each flagged for whether it is final and whether it covers safety only. A safety review is not an efficacy finding, and most reporting in this category conflates the two.
Commission Regulation (EU) 2022/2340 of 30 November 2022, in force 21 December 2022, with a sell-through transition for non-compliant product lawfully on the market before that date until 21 June 2023. It added green tea extracts containing EGCG to Annex III Parts B (restricted) and C (Union scrutiny) of Regulation (EC) No 1925/2006. Verbatim conditions: "Daily portion of food shall contain less than 800 mg of (−)-epigallocatechin-3-gallate"; the label shall indicate EGCG content per portion and the maximum number of portions for daily consumption and warn against reaching 800 mg or more per day; plus three mandatory warnings — "Should not be consumed if you are consuming other products containing green tea on the same day", "Should not be consumed by pregnant or lactating women and children below 18 years old", and "Should not be consumed on an empty stomach". Aqueous extracts that reconstitute into a composition comparable to traditional green tea infusions are excluded.
The statement includes "Do not take on an empty stomach. Take with food", advice against use by people with liver problems, and advice to stop use and consult a practitioner if abdominal pain, dark urine or jaundice occur. It follows the USP comprehensive review, which found a hepatocellular injury pattern, case-report intakes from about 140 mg to roughly 1,000 mg/day, increased catechin bioavailability from repeated bolus doses taken while fasting, and no contribution from solvent residues, pesticides, pyrrolizidine alkaloids or elemental impurities. In the United States the compound remains a dietary supplement: its regulation now consists largely of warnings.
The ANS Panel opinion that is the direct basis for Regulation (EU) 2022/2340. The transaminase finding comes from interventional trial data, not case reports. Catechins from traditionally prepared infusions and equivalent reconstituted drinks were considered generally safe at reported EU intakes, with rare liver-injury cases most likely idiosyncratic. Declining to set a safe dose is the strongest available statement that the safe margin is unknown.
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The proposed mechanism for this ingredient has not been confirmed in humans. Marketing copy frequently states it as settled. It is not.
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