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Benefit and Tolerability of IQP-AE-103 in Weight Loss

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InQpharm

Status

Completed

Conditions

Overweight
Obesity

Treatments

Dietary Supplement: IQP-AE-103 (165mg)
Dietary Supplement: IQP-AE-103 (330mg)
Dietary Supplement: Placebo

Study type

Interventional

Funder types

Industry

Identifiers

NCT03058367
INQ/023314

Details and patient eligibility

About

This study is to evaluate the benefit and tolerability of two dosages of IQP-AE-103 (990mg and 1980mg daily) in reducing body weight in overweight and moderately obese subjects

Enrollment

108 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Age 18 to 65 years
  2. Overweight to moderately obese subjects (BMI ≥ 25 and < 35 kg/m2)
  3. Expressed desire for weight loss
  4. Accustomed to 3 main meals/day
  5. Commitment to take IP as recommended
  6. Commitment to adhere to diet recommendation during the study
  7. Commitment to maintain habitual level of activity/exercise during the study
  8. Consistent and stable body weight for 3 months prior to V1
  9. Commitment to avoid the use of other weight management products or programs during study
  10. Commitment and ability to complete the subject diary and study questionnaires
  11. Females of childbearing potential: negative pregnancy testing (beta HCG-test in urine) at V1, agreement to use appropriate contraception methods during the study period
  12. Consents to participate, understands requirements of the study and is willing to comply

Exclusion criteria

  1. Known sensitivity to the ingredients of the investigational product or source of ingredients
  2. Pregnancy or nursing
  3. Smoking cessation within 6 months prior to V1 or during the study (regular smoking during the study at the same level as prior to the study is allowed)
  4. Current or history of abuse of drugs, alcohol or medication
  5. Clinically relevant excursions of safety laboratory parameter
  6. Diabetes mellitus type 1
  7. Untreated or unstable diabetes mellitus type 2
  8. Untreated or unstable endocrine disorders which may influence body weight (e.g. Cushing's disease, thyroid gland disorders)
  9. Stenosis in the gastrointestinal (GI) tract
  10. Bariatric surgery in subject´s medical history
  11. Abdominal surgery within the last 6 months prior to V1
  12. Current use of medications that may affect body weight (eg. antipsychotics, anti-depressants, corticosteroids etc.)
  13. Presence of acute or chronic gastrointestinal disease (e.g. inflammatory bowel disease, coeliac disease, pancreatitis)
  14. Digestion/absorption disorders in gastrointestinal (GI) tract
  15. History of eating disorders such as bulimia, anorexia nervosa within the past 12 months prior to V1
  16. Other serious organ or systemic diseases such as cancer within the last 5 years prior to V1
  17. Any electronic medical implant
  18. Use of any medication that could influence GI functions such as antibiotics within 4 weeks and any laxatives, opioids, glucocorticoids, anticholinergics within last 3 months prior to V1 and during the study, as per investigator judgement
  19. Any medication or use of products for the treatment of obesity (e.g. orlistat, other fat binder, carbohydrate/starch blocker, fat burner, satiety products etc.) within last 3 months prior to V1 and during the study
  20. Participation in similar studies or weight loss programs within last 4 weeks prior to V1
  21. Participation in other studies during the last 4 weeks prior to V1
  22. Inability to comply
  23. Presence of other factor(s) or medication that should preclude subject participation as per investigator judgement

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

108 participants in 3 patient groups, including a placebo group

High dose IQP-AE-103 (1980mg)
Experimental group
Description:
2 capsules IQP-AE-103 by mouth, three times a day after main meals for 12 weeks
Treatment:
Dietary Supplement: IQP-AE-103 (330mg)
Low dose IQP-AE-103 (990mg)
Experimental group
Description:
2 capsules IQP-AE-103 by mouth, three times a day after main meals for 12 weeks
Treatment:
Dietary Supplement: IQP-AE-103 (165mg)
Placebo
Placebo Comparator group
Description:
2 capsules IQP-AE-103 by mouth, three times a day after main meals for 12 weeks
Treatment:
Dietary Supplement: Placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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