Sepibright™ (Strawberry Leaf Extract — Seppic)

Fragaria × ananassa
Evidence Level
Preliminary
2 Clinical Trials
6 Documented Benefits
1/5 Evidence Score

Sepibright is a hot-water extract of cultivated strawberry leaves (Fragaria × ananassa) from Brittany, France, launched in 2026 by the French ingredient maker Seppic as its first nootropic for dietary supplements, at 300 mg a day. It is standardized to polyphenols and ellagitannins and also carries salidroside, the marker compound of rhodiola. All of its human evidence is one Seppic-funded trial in 109 older adults with memory complaints. That trial's primary statistical analysis did not separate the extract from placebo on any primary or secondary outcome; the memory and stress gains Seppic advertises come from exploratory comparisons that the authors themselves call hypothesis-generating. Seppic's own page says its suggested claims have not been evaluated by regulators. Treat it as an interesting upcycled botanical still waiting for a confirmatory trial.

Studied Dose 300 mg/day (two 150 mg capsules) for 12 weeks, supplying about 20 mg polyphenols and 4 mg ellagitannins
Active Compound Strawberry leaf polyphenols, including ellagitannins and salidroside

Benefits

Studied for episodic memory in older adults

In the only human trial, 300 mg a day for 12 weeks was tested in older adults with self-reported memory complaints. Errors on a visual paired associates learning task fell further on the extract than on placebo at weeks 6 and 12, but only in exploratory comparisons made after the main statistical model found no group difference.

Primary endpoint did not separate from placebo

The trial was registered and sized around spatial working memory errors. That measure did not differ between groups at either visit, and neither did the multitasking test of executive function, fatigue or self-rated memory difficulties. The authors describe the positive signals as hypothesis-generating rather than confirmatory.

What the headline 18 percent figure actually measures

Seppic's figures of 18 percent fewer errors and an 11 percent higher memory score at week 6 are the extract group's change from its own baseline, not the gap versus placebo. The extract group also started with more errors (24.0 versus 19.8, a gap the authors report as not statistically significant), and by week 12 both groups scored almost the same (18.5 versus 18.8), a pattern that can reflect regression toward the average.

Verbal recall gains limited to a younger subgroup

Across the whole trial, verbal word recall and recognition did not differ between groups. After spotting an age interaction, the researchers split participants at age 70; those aged 60 to 69 on the extract recalled about 1.4 more words at week 12, versus 0.2 on placebo. The authors call the size of this change modest and of unclear clinical relevance.

Perceived stress, sleep and fatigue outcomes

Perceived stress fell by about 1.7 points on a 40-point scale in the extract group, and in an exploratory comparison the difference from placebo was statistically significant at week 6 only, not at week 12. The extract group also began with higher stress scores. Insomnia scores improved similarly in both groups, and fatigue did not change in either.

Small daily polyphenol and ellagitannin dose

Each 300 mg daily dose supplied about 20 mg of total polyphenols, including roughly 4 mg of ellagitannins and 3 mg of salidroside. Diet questionnaires showed participants in both groups already took in about 5 to 9 mg of ellagitannins a day from food, so the extract adds a modest amount on top of an ordinary diet rather than a concentrated load.

Mechanism of action

1

Ellagitannins are converted to urolithins by gut bacteria

Ellagitannins and ellagic acid are poorly absorbed as such. Gut bacteria turn them into urolithins, which are absorbed much better than their precursors. Depending on their microbial make-up, people fall into urolithin metabotypes A, B or 0, so the same dose can lead to very different urolithin exposure from person to person.

2

Urolithin A brain effects shown only in animals and cells

Urolithin A restores mitophagy and dampens neuroinflammation in rodent and cell models, and reviewers suggest it may be a final driver of ellagitannin neuroprotection. In people it circulates mostly as glucuronide and sulfate conjugates, the forms reaching the brain are unknown, and no completed trial has tested it on cognitive outcomes.

3

Nrf2 antioxidant signaling in animal studies

In diabetic rats, four weeks of a water extract of strawberry leaves improved water maze performance and lowered hippocampal oxidative and inflammatory markers alongside Nrf2/HO-1 activation. A separate cell and mouse study linked an ethanol leaf extract to Nrf2 activation and protection of dopaminergic neurons. Neither tested Sepibright.

4

Salidroside as a second marker compound

The extract also supplies about 3 mg a day of salidroside, the phenylpropanoid glycoside best known from rhodiola. The trial authors propose it may contribute to the stress result, citing animal work, but the trial measured no blood levels of salidroside, urolithins or cortisol, so any mechanism in people remains untested.

5

Leaves are richer in polyphenols than the fruit

Strawberry leaves are a cultivation by-product; one analysis of the Festival cultivar found about 122-fold higher total polyphenol content and 13-fold higher antioxidant capacity in leaf extracts than in the fruit. That difference is why strawberry fruit trials cannot simply be read across to a leaf extract.

Clinical trials

1
Sepibright in Older Adults with Memory Complaints
PubMed

Randomized, double-blind, placebo-controlled, single-center trial of strawberry leaf extract (Sepibright) 300 mg/day for 12 weeks, registered as NCT06819163, funded by Seppic, with four Seppic employees among the authors (Dormal V, Dudonné S, Gombert C, Laurençon L, Fouilland J, Buchet M, Zacharias I, Copine S, Simar L, Deldicque L 2026, J Nutr Health Aging 30(9):100929, PMID 42508219).

109 adults aged 60 to 80 in Belgium with self-reported memory complaints and preserved global cognition (MMSE above 24); 98 analysed per protocol (50 extract, 48 placebo).

The primary mixed-effects analysis found no significant group-by-time interaction for the registered primary outcome (spatial working memory errors) or any secondary outcome. Exploratory change-from-baseline comparisons favored the extract for paired associates learning errors at weeks 6 and 12 (p = 0.016 and p = 0.048), perceived stress at week 6 only (p = 0.043) and verbal recall in a post hoc subgroup under age 70. Registered secondary outcomes on emotional state (PANAS), self-rated health and self-perceived memory, concentration and attention are not reported in the paper. Possibly related adverse events: 7 on the extract, 9 on placebo, none serious. The sponsor holds the data, which are not publicly available.

2
Freeze-Dried Strawberry Fruit in Older Adults (Class Evidence)
PubMed

Randomized, double-blind, placebo-controlled trial of 24 g/day freeze-dried strawberry powder for 90 days (Miller MG, Thangthaeng N, Rutledge GA, Scott TM, Shukitt-Hale B 2021, Br J Nutr 126(2):253-263, PMID 33468271). Class evidence: whole fruit, not a leaf extract; it did not test Sepibright.

37 healthy adults aged 60 to 75 (22 men, 15 women).

Group-by-visit interactions favored strawberry on a virtual spatial navigation task and on word recognition in the California Verbal Learning Test, while gait and balance did not improve. The authors called for larger, longer trials. It shows some human cognitive signal for strawberry fruit, but the fruit is a different material from the leaf extract sold as Sepibright.

Side effects and drug interactions

Common Potential side effects

In the 12-week trial, possibly related adverse events were no more common than on placebo: 7 on the extract versus 9 on placebo.
Complaints possibly linked to the extract were digestive upset, sleep disturbance, headache and joint pain, each in one to three people.
No serious adverse events occurred, but safety data cover only 12 weeks in about 50 people taking the extract.
People with a known strawberry allergy were excluded from the trial and should avoid it.
No safety data exist for pregnancy, breastfeeding or children.

Important Drug interactions

No interaction studies exist for Sepibright; the points below are general precautions for a polyphenol-rich botanical extract.
Donepezil, memantine and other dementia medicines: not studied together, and people with diagnosed cognitive disorders were excluded from the trial.
Antidepressants, anxiolytics and sedatives: the trial excluded people using medicines that affect cognition or mood, so combined use is unstudied.
Rhodiola or other salidroside-containing supplements: the extract adds a small amount of salidroside, and stacking has not been studied.
Iron supplements: tannin-containing plant extracts may reduce non-heme iron absorption, a theoretical concern at this small dose.

Frequently asked questions about Sepibright™ (Strawberry Leaf Extract — Seppic)

What is Sepibright?

Sepibright is a hot-water extract of cultivated strawberry leaves (Fragaria × ananassa) from Brittany, France, launched in 2026 by the French ingredient maker Seppic as its first nootropic for dietary supplements, at 300 mg a day.

What is Sepibright used for?

Sepibright is researched primarily for Cognitive. In the only human trial, 300 mg a day for 12 weeks was tested in older adults with self-reported memory complaints. Errors on a visual paired associates learning task fell further on the extract than on placebo at weeks 6 and 12, but only i…

What is the recommended dosage of Sepibright?

The clinically studied dose is 300 mg/day (two 150 mg capsules) for 12 weeks, supplying about 20 mg polyphenols and 4 mg ellagitannins Always follow the product label and check with a healthcare provider for personal advice.

Is Sepibright safe, and does it have side effects?

For most healthy adults, Sepibright is well tolerated at studied doses. Reported effects can include: In the 12-week trial, possibly related adverse events were no more common than on placebo: 7 on the extract versus 9 on placebo. Complaints possibly linked to the extract were digestive upset, sleep disturbance, headache and joint pain, each in one to three people. It may also interact with some medications. Sepibright is not right for everyone, so check with a healthcare provider first if you are pregnant or breastfeeding, have a medical condition, or take prescription medication.

Does Sepibright interact with any medications?

Possible interactions include: No interaction studies exist for Sepibright; the points below are general precautions for a polyphenol-rich botanical extract. Donepezil, memantine and other dementia medicines: not studied together, and people with diagnosed cognitive disorders were excluded from the trial. If you take prescription medication, check with a pharmacist or doctor before using it.

How strong is the scientific evidence for Sepibright?

NutraSmarts rates the evidence for Sepibright as Preliminary (1 out of 5). It is backed by 2 clinical trials and 8 cited references summarized on this page. A higher rating reflects more, larger, and better-designed human studies.

References(8 citations)

Evidence ratings on NutraSmarts are based on the totality of human clinical research, with emphasis on randomized controlled trials, meta-analyses, and systematic reviews. The references below directly support claims made throughout this page.

  1. Dormal V, Dudonné S, Gombert C, Laurençon L, Fouilland J, Buchet M, Zacharias I, Copine S, Simar L, Deldicque L. Enhanced memory function and reduced perceived stress in older adults with self-reported memory complaints following strawberry leaf extract supplementation: a randomized, double-blind, placebo-controlled study. J Nutr Health Aging. 2026;30(9):100929..PubMedUsed to support: The only human trial of Sepibright: 109 adults aged 60 to 80 with memory complaints took 300 mg/day or placebo for 12 weeks. The primary mixed-effects analysis found no significant group-by-time interaction for any primary or secondary outcome; exploratory comparisons favored the extract for paired associates learning errors and for week-6 perceived stress. Funded by Seppic, with four Seppic employees among the authors.
  2. Miller MG, Thangthaeng N, Rutledge GA, Scott TM, Shukitt-Hale B. Dietary strawberry improves cognition in a randomised, double-blind, placebo-controlled trial in older adults. Br J Nutr. 2021;126(2):253-263..PubMedUsed to support: Class evidence from strawberry fruit, not leaf: in 37 adults aged 60 to 75, 24 g/day freeze-dried strawberry for 90 days improved virtual spatial navigation and word recognition versus placebo, with no change in gait or balance. It did not test Sepibright.
  3. Zhang L, Ma Q, Zhou Y. Strawberry Leaf Extract Treatment Alleviates Cognitive Impairment by Activating Nrf2/HO-1 Signaling in Rats With Streptozotocin-Induced Diabetes. Front Aging Neurosci. 2020;12:201..PubMedUsed to support: Animal study only: a water extract of strawberry leaves given for 4 weeks to diabetic rats improved Morris water maze performance, lowered hippocampal oxidative stress and inflammatory markers, and activated Nrf2/HO-1 signaling. The extract was prepared in the laboratory, not Sepibright.
  4. Ueda C, Tokumatsu T, Sogame F, Chiba N, Norikura T, Sasaki Y, Matsui-Yuasa I, Kojima-Yuasa A. Strawberry leaf extract protects dopaminergic neurons by restoring redox and mitochondrial homeostasis. Front Nutr. 2026;13:1893670..PubMedUsed to support: Cell and mouse work only: an ethanol extract of Japanese strawberry leaves activated AMPK and Nrf2, supported mitochondrial quality control in neuronal cells, and reduced motor deficits and dopaminergic neuron loss in a rotenone mouse model. It did not test Sepibright or any cognitive outcome in people.
  5. García-Villalba R, Tomás-Barberán FA, Iglesias-Aguirre CE, Giménez-Bastida JA, González-Sarrías A, Selma MV, Espín JC. Ellagitannins, urolithins, and neuroprotection: Human evidence and the possible link to the gut microbiota. Mol Aspects Med. 2023;89:101109..PubMedUsed to support: Review establishing that ellagitannins are poorly absorbed and converted by gut bacteria into urolithins according to metabotypes A, B or 0, that urolithin A brain benefits are consistent in animals but not addressed in humans, and that the urolithin forms reaching the brain are unknown.
  6. Tomás-Barberán FA, González-Sarrías A, García-Villalba R, Núñez-Sánchez MA, Selma MV, García-Conesa MT, Espín JC. Urolithins, the rescue of "old" metabolites to understand a "new" concept: Metabotypes as a nexus among phenolic metabolism, microbiota dysbiosis, and host health status. Mol Nutr Food Res. 2017;61(1). doi:10.1002/mnfr.201500901..PubMedUsed to support: Review supporting the mechanism section: urolithins are produced by the gut microbiota from ellagitannins and ellagic acid, are much better absorbed than their precursors, and are produced very differently from person to person.
  7. Girish Oswal D, Rane M. Is Urolithin A(UA) a pharmacologically credible neuro-nutraceutical? A critical review of mechanisms, brain exposure, and evidence gaps in Alzheimer's and Parkinson's disease. Neurochem Int. 2026;199:106224..PubMedUsed to support: Independent critical review: urolithin A's neuroprotective effects are preclinical, it circulates in humans mainly as glucuronide and sulfate conjugates, and no completed human trial has evaluated cognitive outcomes. Supports the caution that the urolithin pathway is plausible but unproven for brain function.
  8. Salas-Arias K, Irías-Mata A, Sánchez-Kopper A, Hernández-Moncada R, Salas-Morgan B, Villalta-Romero F, Calvo-Castro LA. Strawberry Fragaria x ananassa cv. Festival: A Polyphenol-Based Phytochemical Characterization in Fruit and Leaf Extracts. Molecules. 2023;28(4):1865..PubMedUsed to support: Composition study showing strawberry leaf extracts had 122-fold higher total polyphenol content and 13-fold higher ORAC antioxidant activity than the fruit, which is why fruit and leaf evidence cannot be treated as interchangeable. Not a study of Sepibright.