Eligibility Details:
Inclusion Criteria:
- • Subject is a male or female, 20-45 years of age, inclusive.
- Subject has a BMI of 20.0-24.9 kg/m2, inclusive and weight ≥ 110 lb at screening
visit.
- Subject is willing to maintain his/her usual physical activity pattern throughout
the study period.
- Subject is willing to follow study instructions including compliance with dietary
restrictions, consumption of study beverage, and study visit schedule.
- Subject is judged to be in good health on the basis of the medical history.
- Subject is willing to abstain from alcohol consumption for 24 hours prior to
study visit.
- Exercise to be maintained throughout study duration, including 3 days before
study visit
- Subject is willing to maintain stable dose of current vitamins, minerals,
supplements and medications not interfering with study outcomes, including birth
control, throughout study duration.
- Subject understands the study procedures and signs forms documenting informed
consent to participate in the study and authorization for release of relevant
protected health information to the study Investigator/s and is willing to
complete study procedures
Exclusion Criteria:
- •Subject has fasting finger prick glucose >100 mg/dL.
- Subject has uncontrolled hypertension (systolic blood pressure ≥160 mm Hg or
diastolic blood pressure ≥100 mm Hg) at the screening visit.
- Subject has had major trauma or a surgical event within 2 months of study visit
1.
- Subject has had a weight change ≥4.5 kg within 2 months of visit, taking weight
loss drugs, or has had bariatric surgery or other weight reduction surgery (ie.
liposuction, laser fat removal, etc)
- Subject has a history or presence of clinically important endocrine,
cardiovascular (including, but not limited to, atherosclerotic disease, history
of myocardial infarction, peripheral arterial disease, stroke), pulmonary,
biliary, or gastrointestinal disorders that, in the opinion of the Investigator,
could interfere with the interpretation of the study results.
- Subject has a history or presence of cancer in the prior 2 years, except for
non-melanoma skin cancer.
- Subject has a history of extreme dietary habits, as judged by the Investigator
(e.g., Atkins diet, etc.).
- Subject has a history of an eating disorder (e.g., anorexia nervosa, bulimia
nervosa, or binge eating) diagnosed by a health professional.
- Subject has a known intolerance or sensitivity to any ingredients in the study
products.
- Subject has used medications known to influence carbohydrate metabolism,
including, but not limited to adrenergic blockers, diuretics, hypoglycemic
medications, and systemic corticosteroids 2 weeks prior to visit 1 and throughout
the study.
- Subject taking systemic steroids, extreme alcohol use, or drug user.
- Subject has vein access score less than 7
- Subject is a female, who is pregnant, planning to be pregnant during the study
period or lactating.
- Subject is a current smoker. Past smoker abstinence for less than 2 years.
- Subject has participated in any clinical trial within 30d prior to enrollment.
- No participation in another Sponsored protocol within 6 months prior to
enrollment
common.study.methods.has-drugs-no
common.study.methods.is-healthy-no
