Status:
NOT_YET_RECRUITING
Single Oral Dose Comparative Bioavailability Study of Investigational Product in Healthy Human Subjects Under Fasting Conditions.
Lead Sponsor:
Vedic Lifesciences Pvt. Ltd.
Conditions:
Healthy Volunteer
Eligibility:
All Genders
18-45 years
Phase:
NA
Brief Summary
The sponsor has developed new curcuminoid formulations with the expectation of enhanced bioavailability compared to existing benchmark products. This study aims to evaluate the comparative bioavailabi...
Detailed Description
This study is an open-label, randomized, balanced, single oral dose, four-treatment, four-sequence, four-period, four-way cross-over comparative bioavailability trial designed to assess the bioavailab...
Eligibility Criteria
Inclusion
- 5.1 Able and willing to participate in the study by complying with the protocol procedures as evidenced by a dated and signed informed consent form 9.5.2 Age greater than equal to 18 less than equal to 45 years. 9.5.3 Willing to consume the study product and donate blood. 9.5.4 BMI from 18.5 to 29.9 kg/m². 9.5.5 Subject with normal health as determined by personal medical and medication history, clinical examination and laboratory examinations within the clinically acceptable limits.
- 5.6 Subjects having vital parameters (blood pressure, body temperature, pulse rate and respiratory rate) within acceptable limits.
- 5.7 Non-smokers or mild/moderate smokers with not more than 10 bidis/cigarettes/pipes per day, and willing to abstain from smoking or chewing any tobacco containing products at least 72.00 hours prior to check-in and throughout the sampling points.
- 5.8 Agreeing not to consume food, drink and condiment containing curcumin (e.g. curry), or other curcuminoids (DMC, BDMC) for the whole duration of the study (36 hours pre-dose to 24 hours post-dose in each period).
- 5.9 Good general and mental health in the opinion of the investigator: no clinically significant or relevant abnormalities upon review of medical history or following a physical examination prior to check-in.
- 5.10 If study volunteer is a female and is of child bearing potential practicing an acceptable method of birth control for the duration of the study as judged by the investigator, such as condoms, foams, jellies, diaphragm, intrauterine device (IUD), or abstinence Or She is surgically sterile (had a bilateral tubal ligation, bilateral oophorectomy with or without a hysterectomy and an absence of bleeding for at least 06 months).
Exclusion
- 6.1 Any medical or surgical conditions, which might significantly interfere with the functioning of gastrointestinal tract or may affect absorption of IP and blood forming organ.
- 6.2 Significant history or current evidence of malignancy or chronic - infectious, cardiovascular, renal, hepatic, ophthalmic, pulmonary, neurological, metabolic (endocrine), hematological, gastrointestinal, immunological or psychiatric disease or organ dysfunction.
- 6.3 Any major illness or hospitalization within 90 days prior to first admission to the study.
- 6.4 Use of any depot injection or an implant of any drug within 3 months prior to check-in and throughout the study.
- 6.5 Use of any prescribed medication or OTC (including herbal drugs and vitamin supplements) within 14 days prior to check-in and throughout the study.
- 6.6 Use of botanical dietary supplements during the study or within three months prior to check-in.
- 6.7 Difficulty in swallowing capsules. 9.6.8 History or presence of alcohol abuse in the past one year \[Alcohol abuse will be defined as greater than 14 drinks per week (1 drink equal to 360 mL beer, 150 mL wine, or 45 mL hard liquor)\].
- 6.9 Consumption of alcoholic products within 24.00 hours prior to check-in in each study period and throughout sampling time points.
- 6.10 Positive alcohol breath or urine drug of abuse test during check-in on each study period.
- 6.11 Consumption of xanthine's or its derivative containing food or beverages (e.g. chocolates, tea, coffee or cola drinks) within 48.00 hours prior to check-in and throughout sampling time points.
- 6.12 Consumption of grapefruit or its juice within 72.00 hours prior to check-in in each period and throughout sampling time points.
- 6.13 History of allergy or hypersensitivity intolerance to turmeric or curcumin.
- 6.14 Individuals who, in the opinion of the investigator, are unlikely to be able to comply with the study.
- 6.15 Irritable bowel syndrome. 9.6.16 Current disease states that are contraindicated with dietary supplementation: chronic diarrhea, constipation or abdominal pain, chronic laxatives use.
- 6.17 Pathology which could affect the study results or expose the subject to an additional risk according to the investigator.
- 6.18 Recent gastroenteritis or food borne illness such as confirmed food poisoning (less than 1 month).
- 6.19 Blood donation within 90 Days prior to the initial visit or intending to donate within the next 90 Days.
- 6.20 Low venous capital not allowing blood kinetic sampling. 9.6.21 Known or suspected food allergy, intolerance, or hypersensitivity to any of the study product ingredients and/or of the standard meals (gluten intolerance, celiac disease, etc.) 9.6.22 Chronic drug treatment (for example anticoagulant, antihypertensive medication, thyroid treatment, asthma treatment, anxiolytic, antidepressant, lipid-lowering treatment, corticosteroids, phlebotonic, veino-tonic, drug with impact on blood circulation) excluding oral and local contraceptives.
- 6.23 Currently taking (or during the past 3 months) any botanical dietary supplement.
- 6.24 History of anorexia nervosa, bulimia, or significant eating disorders according to the investigator.
- 6.25 Participation in another clinical trial 90 days prior to check-in period I of this study.
- 6.26 Presenting a psychological or linguistic incapability to sign the informed consent.
- 6.27 Female volunteer who has used implanted or injected hormonal contraceptives anytime during the 06 months prior to check-in or used hormonal contraceptives within 14 days before check-in
Key Trial Info
Start Date :
September 1 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
November 1 2025
Estimated Enrollment :
24 Patients enrolled
Trial Details
Trial ID
NCT07141368
Start Date
September 1 2025
End Date
November 1 2025
Last Update
August 26 2025
Active Locations (1)
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1
IndiGlobal Labs Pvt. Ltd
Hyderabad, Telangana, India, 500051