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B

Supplement · graded by use, three uses

Ginkgo Biloba (EGb 761)

Cognitive symptoms in mild to moderate dementia.

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In plain words

Ginkgo is an extract made from the leaf of the ginkgo tree. The studies used one standard extract at 240 mg a day. In people with mild to moderate dementia, pooled studies of more than 2,500 patients found better thinking scores over about six months. Other reviews disagreed, and most positive studies had ties to the maker. For mild thinking problems, only one study exists. Case reports link it to bleeding with blood thinners, though tests with warfarin found little effect. It may weaken seizure drugs.

The B belongs to one of the three uses graded on this record. The other two carry their own letters.

Grades by use · each use graded on its own evidence
BCognitive symptoms in mild to moderate dementiameasured function
As studied, and the trials
As studied
Dose240 mg a day, where most of the benefit sat (Tan 2015, PMID PubMed ID: the permanent number the US National Library of Medicine gives a published paper. Each one links to that paper's record on PubMed. 25114079; Riepe 2025, PMID 39895346).
FormStandardized Ginkgo biloba leaf extract EGb 761 (Tan 2015, PMID 25114079; Riepe 2025, PMID 39895346).
Population2,561 patients with Alzheimer, vascular or mixed dementia in 9 trials (Tan 2015, PMID 25114079); 782 patients with mild dementia (Riepe 2025, PMID 39895346).
Duration22 to 26 weeks (Tan 2015, PMID 25114079).

Tan et al. (J Alzheimers Dis, 2015; PMID 25114079) and Gauthier and Schlaefke (Clin Interv Aging, 2014; PMID 25506211) found cognition improved; Riepe et al. (World J Biol Psychiatry, 2025; PMID 39895346) agrees in mild dementia. Birks and Grimley Evans (Cochrane, 2009; PMID 19160216) and Thancharoen et al. (Drugs Aging, 2019; PMID 30937879) dissent. Replicated The same finding reproduced by a separate research group. A result seen once can be chance or bias; a replicated one is harder to explain away. trials with dissenting pools fit B, not A. The replicating trials are largely manufacturer-affiliated, which is disclosed here.

CMild cognitive impairmentmeasured function
As studied, and the trials
As studied
Dose240 mg a day (Gavrilova 2014, PMID 24633934).
FormStandardized extract EGb 761 (Gavrilova 2014, PMID 24633934).
Population160 patients with mild cognitive impairment and neuropsychiatric symptoms (Gavrilova 2014, PMID 24633934).
Duration24 weeks (Gavrilova 2014, PMID 24633934).

Gavrilova et al. (Int J Geriatr Psychiatry, 2014; PMID 24633934): neuropsychiatric symptoms and a trail-making test improved against placebo An inactive substitute made to look like the real treatment, so participants cannot tell which one they received.. One trial with manufacturer-affiliated authors, not independently repeated: C.

DDementia prevention in older adultshard clinical endpoint An outcome that matters directly to a person and is counted without judgment, such as death, heart attack, stroke or fracture.
As studied, and the trials
As studied
Dose120 mg twice a day (PMID 19017911, PMID 22959217).
FormStandardized extract EGb 761 (GEM, PMID 19017911; GuidAge, PMID 22959217).
PopulationAdults aged 75 and over (PMID 19017911) and adults aged 70 and over with memory complaints (PMID 22959217).
DurationMedian 6.1 years (PMID 19017911) and 5 years (PMID 22959217).

GEM (DeKosky et al., JAMA, 2008; PMID 19017911): 3,069 adults aged 75 and over, 120 mg twice a day for a median 6.1 years; dementia 3.3 against 2.9 per 100 person-years (hazard ratio How often an event happened in the treated group compared with the control group over the same period. A ratio of 0.80 means 20 percent fewer events. 1.12, 0.94 to 1.33), and no effect on progression in those who entered with mild cognitive impairment. GuidAge (Vellas et al., Lancet Neurol, 2012; PMID 22959217): 2,854 adults aged 70 and over with memory complaints, the same dose of EGb 761 for 5 years; probable Alzheimer's disease 1.2 against 1.4 per 100 person-years (hazard ratio 0.84, 0.60 to 1.18), in a trial funded by the extract's maker. Two large trials, neither preventing dementia: tested, no benefit. This does not grade symptoms in people who already have dementia, which are graded on their own rows.

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B Ginkgo Biloba (EGb 761) structure
Multi-constituent standardized extract
Dose studied
240 mg/day (EGb 761)
Form graded
Standardized EGb 761 leaf extract
B Grade B

A letter describes the human evidence, not the product, the manufacturer, or the ingredient's worth.

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Ginkgo biloba (EGb 761) for cognitive symptoms in mild to moderate dementia, graded on human trial evidence.

RCTWhy this flag? ▾

At least one randomized, placebo-controlled human trial, typically double-blinded Neither the participants nor the people assessing them know who received the real treatment until the trial ends..

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PilotWhy this flag? ▾

Small (typically n<50), exploratory trial. Often open-label Everyone in the trial knows which treatment they are receiving, so expectations can shape the results, especially for symptoms people report themselves.. Hypothesis-generating, not definitive.

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As studied: dose, form, population and duration for every use
As studied
Cognitive symptoms in mild to moderate dementia
FormStandardized Ginkgo biloba leaf extract EGb 761 (Tan 2015, PMID 25114079; Riepe 2025, PMID 39895346).
Dose240 mg a day, where most of the benefit sat (Tan 2015, PMID 25114079; Riepe 2025, PMID 39895346).
Population2,561 patients with Alzheimer, vascular or mixed dementia in 9 trials (Tan 2015, PMID 25114079); 782 patients with mild dementia (Riepe 2025, PMID 39895346).
Duration22 to 26 weeks (Tan 2015, PMID 25114079).
Mild cognitive impairment
FormStandardized extract EGb 761 (Gavrilova 2014, PMID 24633934).
Dose240 mg a day (Gavrilova 2014, PMID 24633934).
Population160 patients with mild cognitive impairment and neuropsychiatric symptoms (Gavrilova 2014, PMID 24633934).
Duration24 weeks (Gavrilova 2014, PMID 24633934).
Dementia prevention in older adults
FormStandardized extract EGb 761 (GEM, PMID 19017911; GuidAge, PMID 22959217).
Dose120 mg twice a day (PMID 19017911, PMID 22959217).
PopulationAdults aged 75 and over (PMID 19017911) and adults aged 70 and over with memory complaints (PMID 22959217).
DurationMedian 6.1 years (PMID 19017911) and 5 years (PMID 22959217).

A grade describes the intervention that was tested. Where the product on the shelf differs from it, this says so.

How this letter has changed · latest: October 2026 · Added
Grade history
October 2026 · Added
Ginkgo: dementia prevention added at Grade D Route 2 Human randomized trials have been run and did not show benefit on the stated outcome. One of the two routes to the lowest letter on EBL's scale.

Two large randomized trials of the standardized extract, GEM (DeKosky et al., JAMA, 2008; PMID 19017911) in 3,069 adults aged 75 and over and GuidAge (Vellas et al., Lancet Neurol, 2012; PMID 22959217) in 2,854 adults with memory complaints, did not prevent dementia or Alzheimer's disease. Prevention now has its own row at D, tested and no benefit. The rows on symptoms in people who already have dementia, and the record's top letter, do not change.PMID 19017911 PMID 22959217

October 2026 · Corrected
Ginkgo: the B scoped to dementia at 240 mg a day; mild cognitive impairment graded C

The record called both of its citations meta-analyses A study that pools the numbers from several trials into one combined estimate. of EGb 761 covering dementia and mild cognitive impairment. Liao et al. (PMID 32658034) did not name EGb 761, and Riepe et al. (PMID 39895346) covered mild dementia only. A PubMed search added Tan et al. (J Alzheimers Dis, 2015; PMID 25114079) and Gauthier and Schlaefke (Clin Interv Aging, 2014; PMID 25506211) for dementia, the dissenting Birks and Grimley Evans (Cochrane, 2009; PMID 19160216) and Thancharoen et al. (Drugs Aging, 2019; PMID 30937879), and the one blinded trial in mild cognitive impairment, Gavrilova et al. (Int J Geriatr Psychiatry, 2014; PMID 24633934), which is graded C on its own.PMID 32658034 PMID 39895346 PMID 25114079 PMID 25506211 PMID 19160216 PMID 30937879 PMID 24633934

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Commercial disclosure
EBL earns no commission on any supplement it grades. A purchase made through the dispensary link below pays EBL nothing, the practitioner discount goes to you in full. The dispensary is Fullscript, a practitioner dispensary, and many of the professional-grade brands in it are sold mainly through practitioners rather than in health food stores. Grades are assigned by published rubric before any commercial relationship exists and are never influenced by one. Full disclosure.

Evidence last reviewed October 2026
Dose

No dose is published here. This record carries no authored dose, because the cited trials do not converge on a single figure. Each trial cited on this page states the dose it used, and EBL has not turned those into a recommendation.

Form note

Standardized extracts were used in the cited trials; product quality varies.

Timing in the trials

The cited reviews pool trials of the extract and do not report when doses were taken (PMID 32658034, PMID 39895346).

Checked against the published summaries; the full papers could not be read. What the cited trials did, not a schedule. Every supplement, by trial timing →

Contraindications A condition or medication that makes a treatment unsafe or unsuitable for a particular person. · read before use
Contraindications and cautions

Seizure disorders. Ginkgo seeds, and to a much smaller degree leaf extracts, contain 4'-O-methylpyridoxine, which antagonizes vitamin B6. Surgery: two weeks of separation is the usual clinical margin. Pregnancy.

Drug Interactions

Anticoagulants and antiplatelets, including warfarin, aspirin and clopidogrel. Ginkgolides antagonize platelet-activating factor, which is the mechanism behind the warning, and published case reports exist. When it was tested, randomized trials found no clinically meaningful effect on INR, on warfarin pharmacokinetics, or on warfarin dose requirement, so the honest position is a monitoring caution rather than a prohibition. Ginkgo induces CYP2C19, which can lower blood levels of drugs cleared by that enzyme. Anticonvulsant effectiveness may be reduced.

Sources for the above

The ginkgo warfarin interaction was tested and did not appear. Randomized trials of ginkgo in warfarin-treated participants found no clinically meaningful effect on INR, on warfarin pharmacokinetics, or on dose requirement, so the case-report-based warning is stronger than what testing showed. Jiang et al. (British Journal of Clinical Pharmacology, 2005; PMID 15801937): randomized trial of the effect of ginkgo and ginger on the pharmacokinetics and pharmacodynamics of warfarin in healthy subjects. Engelsen et al. (Thrombosis and Haemostasis, 2002; PMID 12083489): randomized double-blind placebo-controlled crossover A trial design in which each participant receives both the treatment and the comparison, one after the other, and serves as their own control. of Ginkgo biloba on warfarin dosage in stable long-term warfarin outpatients.

How to track

A validated cognitive assessment (MoCA or ADAS-Cog) at baseline and after 12 weeks to measure the memory and attention outcomes studied in the EGb 761 trials. Subjective cognitive complaints using a standardized self-report scale alongside the objective test. EGb 761 is the specific extract studied: results with other ginkgo preparations are not established.

Primary evidenceSeven papers, each linked to its PubMed record.
Primary evidence

Tan et al. (Journal of Alzheimer's Disease, 2015; PMID 25114079): 9 randomized trials of EGb 761, 2,561 patients, 22 to 26 weeks; cognition, daily activities and clinician global impression favored EGb 761, mainly at 240 mg a day. Gauthier and Schlaefke (Clinical Interventions in Aging, 2014; PMID 25506211): 7 trials, cognition improved. Riepe et al. (World Journal of Biological Psychiatry, 2025; PMID 39895346): pooled subgroup analysis of 4 placebo-controlled trials in 782 patients with mild dementia at 240 mg a day. Liao et al. (Clinical Neuropharmacology, 2020; PMID 32658034): 7 studies, 939 patients with Alzheimer disease, of Ginkgo biloba preparations not named as EGb 761. Not every pool agrees: Birks and Grimley Evans (Cochrane Database of Systematic Reviews A review that searches for every study on a question using a method set in advance, then assesses them together., 2009; PMID 19160216) judged the evidence inconsistent, and Thancharoen et al. (Drugs and Aging, 2019; PMID 30937879) found no benefit over placebo in mild to moderate Alzheimer disease. Several replicating trials and two of the pooled analyses have authors from the manufacturer. Gavrilova et al. (International Journal of Geriatric Psychiatry, 2014; PMID 24633934) is the one blinded trial in mild cognitive impairment.

Educational use only · Not medical advice · Starting, stopping or changing any supplement or medication is a decision for your physician

FDA / DSHEA statement

These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease. The grade on this page describes the strength of published human trial evidence in the populations studied. It is not a recommendation for any individual and is not medical advice. Starting, stopping or changing any supplement or medication is a decision for your physician.

Who responds: this record's trial reading reports no subgroup that identifies who responds.

Independence
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How EBL searched for the trials (1 search)

The search that was run, what it returned, and what was left out and why, so the absence of evidence can be checked as well as its presence.

Searched PubMed in October 2026. 49 records screened, 35 eligible for the graded claim.
Query: ("EGb 761"[tiab] OR EGb761[tiab]) AND (dementia[tiab] OR "mild cognitive impairment"[tiab] OR "cognitive impairment"[tiab]) AND (meta-analysis[pt] OR randomized controlled trial[pt])
Eligibility judged on titles: blinded RCTs Randomized controlled trial: people are assigned to the treatment or a comparison by chance, so the groups differ only in what they received. It is the design that can show cause and effect. or pooled analyses of EGb 761 in dementia or MCI with a cognitive or global endpoint The outcome a trial measures to decide whether the treatment worked, such as heart attacks, blood pressure or a symptom score.. Abstracts read: Gauthier 2014 (PMID 25506211), Tan 2015 (PMID 25114079), Weinmann 2010 (PMID 20236541), Birks 2009 Cochrane (PMID 19160216), Cheng 2026 vascular dementia (PMID 42635820: EGb 761 SKT MD -2.65 from 3 trials, n = 283, I2 92.8%, very low certainty), Gavrilova 2014 MCI RCT (PMID 24633934), Thancharoen 2019 network MA (PMID 30937879), plus the cited Liao 2020 and Riepe 2025. Screened out: healthy-volunteer and cognitively intact trials, prevention methodology (GuidAge, PMID 26624212), cardiovascular events, generalized anxiety, tinnitus and BPSD-only analyses, a pharmacoeconomic analysis, an open-label MCI trial (PMID 37012306) and narrative summaries. Eligible count is title-based and approximate.

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