A Study to Determine the Safety and Tolerability of a Range of Doses of PeptiControl in Pre-diabetic Individuals

Nuritas

Status: Completed

Conditions: Overweight; Pre Diabetes

Treatments: Dietary Supplement: PeptiControl™ (Mid - Dose 870 mg/day); Dietary Supplement: PeptiControl™ (Low - Dose 435 mg/day); Dietary Supplement: Placebo Microcrystalline Cellulose; Dietary Supplement: PeptiControl™ (High - Dose 2610 mg/day)

Study type: Interventional

Funder types: Industry

Identifiers

NCT06440213

NRS/230703/PF/PDI

Details and patient eligibility

About

A randomised, double blind, placebo controlled parallel study to examine the effects of a dose range of PeptiControl, a plant-based ingredient, in pre-diabetic males and females.

Full description

The primary aim of this study is to evaluate safety and establish the effective dose to see acute effects in males and females with elevated fasting blood glucose. PeptiControl will be supplemented 30 minutes before lunch as a single oral dose of either 2610mg, 870mg or 435mg/day. A placebo group will also be included who will receive microcrystalline cellulose. Capsule number will be matched across all study arms to retain double blinding.

This trial incorporates continuous glucose monitoring (CGM) as wearable technology to measure blood glucose and time in range of the participants for the duration of the study. The trial will be conducted over 12 days, which includes a 2 day run-in period to gather baseline CGM data, followed by 6 days of PeptiControl supplementation and 4 days follow up on safety and blood glucose tracking post supplementation.

The primary endpoint will measure safety and tolerability via adverse event reporting and occurrence of hypoglycemic episodes evaluated by time below target range (70 - 180 mg/dL) during CGM throughout the intervention.

Secondary endpoints investigated during the trial will include safety of a dose range as assessed by a safety blood panel, glucose metabolism and insulin sensitivity, time in range, aspects of cognition and memory and hunger, satiety and fullness as assessed by VAS questionnaires.

Enrollment: 132 patients

Sex: All

Ages: 30 to 60 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Males and Females (30-60 years of age)
• Individuals with Body Mass Index (BMI) more than or equal to 25 and less than or equal to 33.0 kg/m²
• Individuals with fasting blood glucose (FBG) more than or equal to 100 mg/dL and less than or equal to 125 mg/dL after 8-10 hours fasting.
• Individual must be a non-smoker or an ex-smoker (5 years or more).
• Have a stable body weight (less than or equal to 4.5 kgs change) in the last 3 months (as self-reported by the individual).
• Be willing to maintain existing dietary habits and physical activity levels throughout the study period.
• Individual must be willing to wear a continuous glucose monitor during the specific time in the study
• Individual must be willing to attend all site visits and follow protocols for that visit, e.g., arrive fasting and provide blood samples.
• Individuals who have given their signed Informed Consent.

Exclusion criteria

• Individuals having fasting blood glucose levels less than 100 mg/dL or more than 125 mg/dL.
• Individuals having BMI outside the range of 25 - 33 kg/m².
• Individuals who are presently dieting, or who were using medications affecting body weight or who had experienced a change in weight of more than 4.5 kg or a change in physical activity within the six months preceding the screening visit.
• Individuals diagnosed with Type I Diabetes mellitus.
• Individuals diagnosed with Type II Diabetes mellitus and currently on medication.
• Individuals with Triglyceride levels more than 200 mg/dL, and/or liver function tests (AST, ALT) levels 1.5 times than the normal range, and/or kidney function test (serum creatinine) levels 1.5 times than the normal range.
• Individuals with low haemoglobin or haematocrit (i.e., lower than normal ranges [less than 12.0 g/dL hemoglobin levels in women and less than 13.0 g/dL hemoglobin levels in men])
• Individuals having a significant acute or chronic co-existing illnesssuch as cardiovascular disease, chronic kidney or liver disease, gastrointestinal disorder, endocrine disorder, immunological disorder, metabolic disease, or any condition which contraindicates, in the investigator's judgement, entry to the study or which poses a significant risk to the individual.
• Individuals diagnosed with hypertension (systolic blood pressure more than 140 mm Hg and/or diastolic blood pressure more than 90 mm Hg) and currently on medication.
• Individuals who have unstable medical conditions or who are on chronic medication that has not been at a stable dose for at least 1 month.
• Consumption of more than the recommended alcohol guidelines i.e., more than 21 alcohol units/week for males and more than 14 alcohol units/week for females.
• Currently or recently (within 3 months of study entry) taking any medication, which in the opinion of the investigator, could interfere with the outcome of the study, including insulin, acetylsalicylic acid, thyroxine, beta blockers, or hypolipidemic agents.
• Individuals on any medications associated with weight loss such as medication for the treatment of deficit hyperactivity, medication associated with weight gain like antipsychotics, or glucocorticoids, and/or immunosuppressants.
• Have a known allergy or sensitivity to any compounds in the test material's active or inactive ingredients or placebo.
• Individuals having a history of drug or alcohol abuse.
• Individuals who have a history of neurological disorders or significant psychiatric illness, who are cognitively impaired and/or who are unable to give informed consent.
• Present or recent use (within 3 months of pre-screening) of dietary supplements that may affect the level of blood glucose, e.g., chromium, dietary fibres, and non-digestible carbohydrates e.g., fructooligosaccharides chicory inulin, mulberry leaf extract.
• Females who are pregnant, lactating or wish to become pregnant during the study.
• Individuals with evidence of a clinically unstable disease (such as depression), as determined by medical history, physical examination, that, in the Investigator and medical monitors opinion, preclude entry into the study.
• Breast feeding women.
• Immune compromised individuals.
• Individuals who have participated in a clinical study with an investigational product (IP) within 90 days before pre-screening, or who plan to participate in another study during the study period.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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132 participants in 4 patient groups, including a placebo group

PeptiControl™ (Low - Dose 435 mg/day)

Active Comparator group

Description:

6 capsules, 30 minutes prior to lunch every day for 6 days

Treatment:

Dietary Supplement: PeptiControl™ (Low - Dose 435 mg/day)

PeptiControl™ (Mid - Dose 870 mg/day)

Active Comparator group

Description:

6 capsules, 30 minutes prior to lunch every day for 6 days

Treatment:

Dietary Supplement: PeptiControl™ (Mid - Dose 870 mg/day)

PeptiControl™ (High - Dose 2610 mg/day)

Active Comparator group

Description:

6 capsules, 30 minutes prior to lunch every day for 6 days

Treatment:

Dietary Supplement: PeptiControl™ (High - Dose 2610 mg/day)

Placebo Microcrystalline Cellulose

Placebo Comparator group

Description:

6 capsules, 30 minutes prior to lunch every day for 6 days

Treatment:

Dietary Supplement: Placebo Microcrystalline Cellulose