Efficacy and Safety of IQP-AK-102 in Reducing Appetite

InQpharm

Status: Completed

Conditions: Energy Intake; Appetite Suppression; Appetite Regulation

Treatments: Device: IQP-AK-102

Study type: Interventional

Funder types: Industry

Identifiers

NCT02774486

INQ/025115

Details and patient eligibility

About

The primary cause of being overweight is an imbalance in calories consumed and energy expenditure. A surplus in energy intake might result in body fat deposition and thereby body weight gain. Therefore, food intake regulation is crucial to control the body weight gain.

Appetite regulation plays an important role in determining the food intake, which is a complex process influenced by the individual (physiology and psychology) and environment. Satiation (process that leads to the termination of eating) and satiety (decline in hunger, increase in fullness after a meal has finished) are the precursors of appetite regulation, which may be induced by various food components such as macronutrients, water, alcohol and non-digestible polysaccharides. High viscosity and swellable/bulking food components such as dietary fibre are expected to elicit stronger satiation/satiety than the macronutrients or clear liquid. Due to its unique physicochemical properties, dietary fibre has been recognized as potential ingredient that helps to enhance the sensation of satiety in the upper gut by increasing gastric distension and delaying gastric emptying, which subsequently reduces the food intake.

IQP-AK-102 comprises of a proprietary blend of dietary fibres known to promote a feeling a fullness. The objectives of this study are to evaluate the efficacy and safety of IQP-AK-102 on appetite reduction in overweight subjects during a 4-weeks interval.

Enrollment: 36 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Males and females, aged 18-65 years
2. BMI ≥25 and BMI <30 kg/m2
3. Generally in good health
4. Regular daily consumption of 3 main meals (breakfast, lunch, dinner)
5. Consistent regular physical activity (≤4 hours of strenuous sportive activity per week) AND willingness to maintain the same level of sport activity throughout the study
6. Commitment to avoid the use of other weight loss and/or management products / programmes during the study
7. Commitment to complete the subject diary correctly and to adhere to the lifestyle recommended for this study
8. Stable concomitant medications (if any)
9. Stable body weight for the last 3 months prior to V1 (less than 5% self-reported change)
10. Subject's agreement to comply with study procedures
11. Negative pregnancy testing (beta HCG-test in urine) at V1 in females of childbearing potential
12. Women of child-bearing potential: willingness to use reliable method of contraception during the study period

Exclusion criteria

1. Known sensitivity to the components of the investigational product
2. Bariatric surgery in the last 12 months prior to V1
3. Abdominal surgery within the last 6 months prior to V1
4. Presence of any active gastrointestinal disease incl. stenosis in the gastrointestinal tract
5. Malabsorption disorders
6. Pancreatitis
7. History of eating disorders like bulimia, anorexia nervosa, binge-eating (within the last 12 months prior to V1)
8. Lack of appetite for any (unknown) reason
9. Use of medications that could influence gastrointestinal functions such as antibiotics, laxatives, opioids, anticholinergics, anti-diarrheals 3 months prior to V1 and during the study
10. Use of medications that could influence body weight (e.g. antidepressants) in the last 3 months prior to V1 and during the study
11. Any medication or use of products for the treatment of obesity (e.g. fat binder, fat burner, satiety products etc.) or treatment that could influence food absorption, in last 3 months before V1 and during the study
12. Gluten allergy
13. History of abuse of drugs, alcohol or medication
14. Exceeding moderate alcohol consumption (≥21 units /week; 1 unit is equal 1⁄2 l of beer, or 200 ml of wine, or 50 ml hard liquor)
15. Smoking cessation within 6 months prior to V1 or during the study (regular smoking at the same level as prior to the study during the study is not an exclusion criteria)
16. Inability to comply with study procedures (e.g. due to language difficulties etc.)
17. Participation in similar studies or weight loss programs within the last 6 months prior to V1 and during the study
18. Participation in other clinical studies within the last 30 days prior to V1 and during the study
19. Clinically relevant deviations of laboratory values
20. Any other reason deemed suitable for exclusion, per investigator's judgement

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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36 participants in 1 patient group

IQP-AK-102

Experimental group

Description:

2 capsules to be taken 3 times daily orally, 30 min before each main meal (breakfast, lunch, dinner) with 250 mL of water

Treatment:

Device: IQP-AK-102