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A Two-part Study of Lembas Edge Evaluating Tolerability and Postprandial Glycemic Control

16 juli 2026 uppdaterad av: Lembas

The goal of part 1 of this clinical trial is to investigate the tolerability of Lembas Edge in healthy adults. The objective of Part 2 of this study is to investigate the efficacy of Lembas Edge on postprandial glycemic control in prediabetic overweight and obese adults. The main questions it aims to answer are:

  • What is the tolerability of Lembas Edge?
  • What is the efficacy of Lembas Edge on postprandial glycemic control?

Researchers will compare Lembas Edge to placebo to see its effects. Participants will be asked to:

  • Provide blood samples.
  • Record their food and beverage intake in Part 2.
  • Complete a satiety questionnaire in Part 2.
  • Consume Lembas Edge or placebo as instructed.

Studieöversikt

Studietyp

Interventionell

Inskrivning (Beräknad)

35

Fas

  • Inte tillämpbar

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

Studieorter

    • Ontario
      • London, Ontario, Kanada
        • KGK Science Inc.

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Vuxen
  • Äldre vuxen

Tar emot friska volontärer

Ja

Beskrivning

Inclusion Criteria Part 1:

  1. Males & females 18 years and older
  2. Females not of child-bearing potential, defined as those who have undergone a sterilization procedure (e.g. hysterectomy, bilateral oophorectomy, bilateral tubal ligation, complete endometrial ablation) or have been post-menopausal for at least 1 year prior to screening Or, Individuals of child-bearing potential must have a negative baseline urine pregnancy test and agree to use a medically approved method of birth control for the duration of the study. All hormonal birth control must have been in use for a minimum of three months. Acceptable methods of birth control include:

    • Hormonal contraceptives including oral contraceptives, hormone birth control patch (Ortho Evra), vaginal contraceptive ring (NuvaRing), injectable contraceptives (Depo-Provera, Lunelle), or hormone implant (Norplant System)
    • Double-barrier method
    • Intrauterine devices
    • Non-heterosexual lifestyle and agrees to use contraception if planning on changing to heterosexual partner(s)
    • Vasectomy of partner at least 6 months prior to screening
    • Abstinence and agrees to use contraception if planning on becoming sexually active during the study
  3. Agrees to maintain current lifestyle habits (diet, physical activity, medications, supplements, and sleep) as much as possible throughout the study
  4. Provided voluntary, written, informed consent to participate in the study
  5. Healthy as determined by medical history as assessed by the Qualified Investigator (QI)

Inclusion Criteria Part 2:

  1. Males & females 18 years and older
  2. Body Mass Index (BMI) between 25.0 and 34.9 kg/m2
  3. Females not of child-bearing potential, defined as those who have undergone a sterilization procedure (e.g. hysterectomy, bilateral oophorectomy, bilateral tubal ligation, complete endometrial ablation) or have been post-menopausal for at least 1 year prior to screening Or, Individuals of child-bearing potential must have a negative baseline urine pregnancy test and agree to use a medically approved method of birth control for the duration of the study. All hormonal birth control must have been in use for a minimum of three months. Acceptable methods of birth control include:

    • Hormonal contraceptives including oral contraceptives, hormone birth control patch (Ortho Evra), vaginal contraceptive ring (NuvaRing), injectable contraceptives (Depo-Provera, Lunelle), or hormone implant (Norplant System)
    • Double-barrier method
    • Intrauterine devices
    • Non-heterosexual lifestyle and agrees to use contraception if planning on changing to heterosexual partner(s)
    • Vasectomy of partner at least 6 months prior to screening
    • Abstinence and agrees to use contraception if planning on becoming sexually active during the study
  4. Hemoglobin A1c (HbA1c) of 5.7-6.4% at screening
  5. Willingness to complete questionnaires, records and diaries associated with the study and to complete clinic visits
  6. Agrees to maintain current lifestyle habits (diet, physical activity, medications, supplements, and sleep) as much as possible throughout the study
  7. Provided voluntary, written, informed consent to participate in the study
  8. Healthy as determined by medical history as assessed by the Qualified Investigator (QI)

Exclusion Criteria Part 1:

  1. Individuals who are pregnant, breast feeding, or planning to become pregnant during the study
  2. Allergy (including alpha-gal syndrome), sensitivity, intolerance, or dietary restriction preventing consumption of investigational product
  3. Unstable metabolic disease or chronic diseases as assessed by the QI
  4. Current or history of any significant diseases of the gastrointestinal tract as assessed by the QI
  5. Unstable hypertension. Treatment on a stable dose of medication for at least 3 months will be considered by the QI (See Section 7.3)
  6. Type I or Type II diabetes
  7. Significant cardiovascular event in the past 6 months. Participants with no significant cardiovascular event on stable medication may be included after assessment by the QI on a case-by-case basis
  8. History of or current diagnosis with kidney and/or liver diseases as assessed by the QI on a case-by-case basis, with the exception of history of kidney stones in participants who are symptom free for 6 months
  9. Self-reported confirmation of current or pre-existing thyroid condition. Treatment on a stable dose of medication for at least 3 months will be considered by the QI
  10. Major surgery in the past 3 months or individuals who have planned surgery during the course of the study. Participants with minor surgery will be considered on a case-by-case basis by the QI
  11. Cancer, except skin basal cell carcinoma completely excised with no chemotherapy or radiation with a follow up that is negative. Volunteers with cancer in full remission for more than five years after diagnosis are acceptable
  12. Individuals with an autoimmune disease or are immune compromised as assessed by the QI
  13. Self-reported confirmation of a Human Immunodeficiency Virus (HIV)-, Hepatitis B- and/or C-positive diagnosis as assessed by the QI
  14. Self-reported confirmation of blood/bleeding disorders as assessed by the QI
  15. Use of prescribed medical cannabinoid products
  16. Chronic use of cannabinoid products (>2 times/week). Occasional users will be required to washout and abstain for the duration of the study period
  17. Regular use of tobacco or nicotine products in the past six months, as assessed by the QI. Occasional users will be required to washout and abstain for the duration of the study period
  18. Alcohol intake average of >2 standard drinks per day as assessed by the QI
  19. Alcohol or drug abuse within the last 12 months
  20. Current use of prescribed and/or over-the-counter (OTC) medications, supplements, and/or consumption of food/drinks that may impact the safety of the investigational product (Sections 7.3.1 and 7.3.2)
  21. Blood donation 30 days prior to baseline, during the study, or a planned donation within 30 days of the last study visit
  22. Participation in other clinical research studies 30 days prior to baseline, as assessed by the QI
  23. Individuals who are unable to give informed consent
  24. Any other condition or lifestyle factor, that, in the opinion of the QI, may adversely affect the participant's ability to complete the study or its measures or pose significant risk to the participant

Exclusion Criteria Part 2:

  1. Individuals who are pregnant, breast feeding, or planning to become pregnant during the study
  2. Allergy (including alpha-gal syndrome), sensitivity, intolerance, or dietary restriction preventing consumption of investigational product or placebo ingredients or the standardized meal
  3. Poor venous access as assessed by the QI
  4. Change in body weight greater than 5 kg within 3 months prior to starting study
  5. Currently on or planning to initiate a body weight reduction diet during the study
  6. Self reported vigorous exercise >120 minutes/week
  7. Obesity induced by endocrinologic or genetic disorders or monogenetic or syndromic forms of obesity
  8. Family or personal history of medullary thyroid carcinoma (MTC) or multiple endocrine neoplasia syndrome type 2 (MEN-2)
  9. Unstable metabolic disease or chronic diseases, including pancreatitis, as assessed by the QI
  10. Current diagnosis with gastroesophageal reflux disease (GERD) or hiatal hernia
  11. Current or history of any significant diseases of the gastrointestinal tract as assessed by the QI
  12. Unstable hypertension. Treatment on a stable dose of medication for at least 3 months will be considered by the QI (See Section 7.3)
  13. Type I or Type II diabetes
  14. Significant cardiovascular event in the past 6 months. Participants with no significant cardiovascular event on stable medication may be included after assessment by the QI on a case-by-case basis
  15. History of or current diagnosis with kidney and/or liver diseases as assessed by the QI on a case-by-case basis, with the exception of history of kidney stones in participants who are symptom free for 6 months
  16. Self-reported confirmation of current or pre-existing thyroid condition. Treatment on a stable dose of medication for at least 3 months will be considered by the QI
  17. Major surgery in the past 3 months or individuals who have planned surgery during the course of the study. Participants with minor surgery will be considered on a case-by-case basis by the QI
  18. Cancer, except skin basal cell carcinoma completely excised with no chemotherapy or radiation with a follow up that is negative. Volunteers with cancer in full remission for more than five years after diagnosis are acceptable
  19. Individuals with an autoimmune disease or are immune compromised as assessed by the QI
  20. Self-reported confirmation of a HIV-, Hepatitis B- and/or C-positive diagnosis as assessed by the QI
  21. Self-reported confirmation of blood/bleeding disorders as assessed by the QI
  22. Use of prescribed medical cannabinoid products
  23. Chronic use of cannabinoid products (>2 times/week). Occasional users will be required to washout and abstain for the duration of the study period
  24. Regular use of tobacco or nicotine products in the past six months, as assessed by the QI. Occasional users will be required to washout and abstain for the duration of the study period
  25. Alcohol intake average of >2 standard drinks per day as assessed by the QI
  26. Alcohol or drug abuse within the last 12 months
  27. Current use of prescribed and/or over-the-counter (OTC) medications, supplements, and/or consumption of food/drinks that may impact the glucose metabolism or efficacy of the investigational product (Sections 7.3.1 and 7.3.2)
  28. Blood donation 30 days prior to baseline, during the study, or a planned donation within 30 days of the last study visit
  29. Participation in other clinical research studies 30 days prior to baseline, as assessed by the QI
  30. Individuals who are unable to give informed consent
  31. Any other condition or lifestyle factor, that, in the opinion of the QI, may adversely affect the participant's ability to complete the study or its measures or pose significant risk to the participant

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: Randomiserad
  • Interventionsmodell: Crossover tilldelning
  • Maskning: Fyrdubbla

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: Low Dose Lembas Edge
Participants will be instructed to take 3 capsules of the study product in a fasted state 120 minutes before a standardized breakfast.
Participants will be instructed to take 3 capsules of the study product in a fasted state 120 minutes before a standardized breakfast.
Experimentell: Medium Dose Lembas Edge
Participants will be instructed to take 3 capsules of the study product in a fasted state 120 minutes before a standardized breakfast.
Participants will be instructed to take 3 capsules of the study product in a fasted state 120 minutes before a standardized breakfast.
Experimentell: High Dose Lembas Edge
In part 1, participants will be instructed to take 3 capsules daily (as a single dose) in the morning until the day prior to their end of study visit (Day 13). In part 2, participants will be instructed to take 3 capsules of the study product in a fasted state 120 minutes before a standardized breakfast.

In part 1, participants will be instructed to take 3 capsules daily (as a single dose) in the morning until the day prior to their end of study visit (Day 13).

In part 2, participants will be instructed to take 3 capsules of the study product in a fasted state 120 minutes before a standardized breakfast.

Placebo-jämförare: Placebo
In part 1, participants will be instructed to take 3 capsules daily (as a single dose) in the morning until the day prior to their end of study visit (Day 13). In part 2, participants will be instructed to take 3 capsules of the study product in a fasted state 120 minutes before a standardized breakfast.
In part 1, participants will be instructed to take 3 capsules daily (as a single dose) in the morning until the day prior to their end of study visit (Day 13). In part 2, participants will be instructed to take 3 capsules of the study product in a fasted state 120 minutes before a standardized breakfast.

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Incidence of post-emergent adverse events (AE)
Tidsram: Day 0 to 14
Part 1. Incidence of post-emergent adverse events (AE)
Day 0 to 14
Clinically relevant changes in blood pressure after supplementation
Tidsram: Day 0 to 14
Part 1. Clinically relevant changes in blood pressure (mmHg) after supplementation
Day 0 to 14
Clinically relevant changes in heart rate after supplementation
Tidsram: Day 0 to 14
Part 1. Clinically relevant changes in heart rate (beats per minute) after supplementation
Day 0 to 14
Clinically relevant changes in aspartate aminotransferase
Tidsram: Day 0 to 14
Part 1. Clinically relevant changes in aspartate aminotransferase (U/L) after supplementation.
Day 0 to 14
Clinically relevant changes in alanine aminotransferase
Tidsram: Day 0 to 14
Part 1. Clinically relevant changes in alanine aminotransferase (U/L) after supplementation.
Day 0 to 14
Clinically relevant changes in alkaline phosphatase
Tidsram: Day 0 to 14
Part 1. Clinically relevant changes in alkaline phosphatase (U/L) after supplementation.
Day 0 to 14
Clinically relevant changes in total bilirubin
Tidsram: Day 0 to 14
Part 1. Clinically relevant changes in total bilirubin (micromole/litre) after supplementation.
Day 0 to 14
Clinically relevant changes in creatinine
Tidsram: Day 0 to 14
Part 1. Clinically relevant changes in creatinine (micromole/litre) after supplementation.
Day 0 to 14
Clinically relevant changes in sodium
Tidsram: Day 0 to 14
Part 1. Clinically relevant changes in sodium (mmol/L) after supplementation.
Day 0 to 14
Clinically relevant changes in potassium
Tidsram: Day 0 to 14
Part 1. Clinically relevant changes in potassium (mmol/L) after supplementation.
Day 0 to 14
Clinically relevant changes in chloride
Tidsram: Day 0 to 14
Part 1. Clinically relevant changes in chloride (mmol/L) after supplementation.
Day 0 to 14
Clinically relevant changes in estimated glomerular filtration rate
Tidsram: Day 0 to 14
Part 1. Clinically relevant changes in estimated glomerular filltration rate (mL/min/1.73 m^2) after supplementation.
Day 0 to 14
Clinically relevant changes in glucose
Tidsram: Day 0 to 14
Part 1. Clinically relevant changes in glucose (mmol/L) after supplementation.
Day 0 to 14
Clinically relevant changes in red blood cell count
Tidsram: Day 0 to 14
Part 1. Clinically relevant changes in red blood cell count (x 10^12/L) after supplementation
Day 0 to 14
Clinically relevant changes in white blood cell count
Tidsram: Day 0 to 14
Part 1. Clinically relevant changes in white blood cell count (x 10^9/L) after supplementation
Day 0 to 14
Clinically relevant changes in platelet count
Tidsram: Day 0 to 14
Part 1. Clinically relevant changes in platelet count (x 10^9/L) after supplementation
Day 0 to 14
Clinically relevant changes in hemoglobin
Tidsram: Day 0 to 14
Part 1. Clinically relevant changes in hemoglobin (g/L) after supplementation
Day 0 to 14
Clinically relevant changes in hematocrit
Tidsram: Day 0 to 14
Part 1. Clinically relevant changes in hematocrit (L/L) after supplementation
Day 0 to 14
Clinically relevant changes in red blood cell indices (MCV - Mean Corpuscular Volume)
Tidsram: Day 0 to 14
Part 1. Clinically relevant changes in MCV (fL) after supplementation
Day 0 to 14
Clinically relevant changes in red blood cell indices (MCH - Mean Corpuscular Hemoglobin)
Tidsram: Day 0 to 14
Part 1. Clinically relevant changes in MCH (pg) after supplementation
Day 0 to 14
Clinically relevant changes in red blood cell indices (MCHC - Mean Corpuscular Hemoglobin Concentration)
Tidsram: Day 0 to 14
Part 1. Clinically relevant changes in MCHC (g/L) after supplementation
Day 0 to 14
Clinically relevant changes in RDW - Red Cell Distribution Width
Tidsram: Day 0 to 14
Part 1. Clinically relevant changes in RDW (%) after supplementation
Day 0 to 14
Clinically relevant changes in red blood cell indices (MPV - Mean Platelet Volume)
Tidsram: Day 0 to 14
Part 1. Clinically relevant changes in MPV (fL) after supplementation
Day 0 to 14
The difference in postprandial glucose between Lembas Edge and placebo
Tidsram: Visit 2 (day 1) to Visit 5 (day 22)
Part 2. The difference in postprandial glucose, as assessed by incremental area under the curve (iAUC) (0-120 min), between Lembas Edge (high dose, medium dose, low dose) and placebo.
Visit 2 (day 1) to Visit 5 (day 22)
The height of the postprandial glucose peak and nadir post meal between Lembas Edge and placebo
Tidsram: Visit 2 (day 1) to Visit 5 (day 22)
Part 2. The height of the postprandial glucose peak and nadir post meal between Lembas Edge (high dose, medium dose, low dose) and placebo.
Visit 2 (day 1) to Visit 5 (day 22)

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
The difference in postprandial glucose iAUC (0-240 min) between Lembas Edge and placebo
Tidsram: Visit 2 (day 1) to Visit 5 (day 22)
Part 2. The difference in postprandial glucose, as assessed by iAUC (0-240 min), between Lembas Edge (high dose, medium dose, low dose) and placebo
Visit 2 (day 1) to Visit 5 (day 22)
The difference in postprandial insulin between Lembas Edge and placebo
Tidsram: Visit 2 (day 1) to Visit 5 (day 22)
Part 2. The difference in postprandial insulin, as assessed by iAUC (0-120 min) and iAUC (0-240 min), between Lembas Edge (high dose, medium dose, low dose) and placebo
Visit 2 (day 1) to Visit 5 (day 22)
The difference in self-reported satiety scores between Lembas Edge and placebo
Tidsram: Visit 2 (day 1) to Visit 5 (day 22)
Part 2. The difference in self-reported satiety scores, as assessed by iAUC (0-240 min), between Lembas Edge (high dose, medium dose, low dose) and placebo
Visit 2 (day 1) to Visit 5 (day 22)

Andra resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Change in fasting glucose from baseline to day 14 after supplementation
Tidsram: Day 0 to 14
Part 1. The change in fasting glucose from baseline to day 14 after supplementation
Day 0 to 14
Change in fasting insulin from baseline to day 14 after supplementation
Tidsram: Day 0 to 14
Part 1. The change in fasting insulin from baseline to day 14 after supplementation
Day 0 to 14
Change in fasting HOMA-IR from baseline to day 14 after supplementation
Tidsram: Day 0 to 14
Part 1. The change in Homeostasis Model Assessment of Insulin Resistance (HOMA-IR) from baseline to day 14 after supplementation
Day 0 to 14
Part 2. Incidence of post-emergent adverse events (AE)
Tidsram: Visit 1 (day -45 to -1) to visit 5 (day 22)
Part 2. Incidence of post-emergent adverse events (AE)
Visit 1 (day -45 to -1) to visit 5 (day 22)
The difference in postprandial peptide YY (PYY) between Lembas Edge and placebo
Tidsram: Day 1 to 22
Part 2. The difference in postprandial PYY, as assessed by iAUC (0-240 min), between Lembas Edge (high dose, medium dose, low dose) and placebo
Day 1 to 22
The difference in postprandial GIP (Glucose-Dependent Insulinotropic Polypeptide) between Lembas Edge and placebo
Tidsram: Day 1 to 22
Part 2. The difference in postprandial GIP, as assessed by iAUC (0-240 min), between Lembas Edge (high dose, medium dose, low dose) and placebo
Day 1 to 22
The difference in postprandial Glucagon-Like Peptide-1 (GLP-1) between Lembas Edge and placebo
Tidsram: Day 1 to 22
Part 2. The difference in postprandial GLP-1, as assessed by iAUC (0-240 min), between Lembas Edge (high dose, medium dose, low dose) and placebo
Day 1 to 22

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Sponsor

Samarbetspartners

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Beräknad)

1 september 2026

Primärt slutförande (Beräknad)

1 januari 2027

Avslutad studie (Beräknad)

1 januari 2027

Studieregistreringsdatum

Först inskickad

14 juli 2026

Först inskickad som uppfyllde QC-kriterierna

16 juli 2026

Första postat (Faktisk)

17 juli 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

17 juli 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

16 juli 2026

Senast verifierad

1 juli 2026

Mer information

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Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Nej

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

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