Informal, Open Label Clinical Trial Results

• We conducted an informal, open-label, proof-of-concept human clinical study among type 1 diabetics in the "friends and family" category, using a crossover design. When the subjects were significantly hyperglycemic, they self-medicated by following either the active control or experimental procedure as described here.

• For the active control, the significantly hyperglycemic type 1 subject consumed eight ounces of water, took insulin as appropriate in accordance with their habits and insulin pump recommendation, and waited until their blood glucose levels were no longer hyperglycemic. Blood glucose levels were recorded every 15 minutes after the intervention was commenced until blood glucose levels dropped to less than 180 mg/dL.

• For the experimental treatment tests, the significantly hyperglycemic subject consumed at least 8 ounces of water along with a therapeutic dosage of a prototype formulation comprising Boliss's active ingredient, took insulin as appropriate in accordance with their habits and pump recommendation, and waited until their blood glucose levels were no longer hyperglycemic. Blood glucose levels were recorded every 15 minutes after the intervention was commenced until blood glucose levels dropped to less than 180 mg/dL. The average starting blood glucose levels were approximately 320 mg/dL for both groups.

• The experimental procedure resulted in reduced duration and magnitude of hyperglycemic events. On average, hyperglycemic blood glucose levels dropped below hyperglycemic levels in less than one hour when type 1 diabetics were subjected to the experimental treatment procedure. In contrast, when subjected to the active control procedure, it took an average of roughly 2.5 hours to return to sub-hyperglycemic blood glucose levels of less than 180 mg/dL.

• This is an enormous difference, particularly given the physical discomfort associated with hyperglycemia, the risk of ketoacidosis when high levels of hyperglycemia persist for long periods, and that the duration and magnitude of hyperglycemic events are believed to correlate closely with A1C levels, which correlate with long-term complications of diabetes.

• Boliss has had mixed results for insulin dependent and non- insulin dependent type 2s. Insulin dependent type 2s have had much more success then those type 2s who do not use insulin, however, we can not guarantee success. Use at your own discretion. Boliss should not be taken by anyone with a sodium restrictive diet.

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• Experimental evidence suggests that diabetics should not necessarily avoid sodium. For instance, a recent paper based on a prospective cohort study, which looked at the correlation between sodium and outcomes in Type 2 diabetic patients, concluded that "lower 24-h urinary sodium excretion was paradoxically associated with increased all-cause and cardiovascular mortality."(1) Therefore, insufficient sodium intake can increase the risk of long-term complications such as cardiovascular disease.

• In the FinnDiane Study, a nationwide multicenter study between 1998 and 2002, 2,807 adults with type 1 diabetes were followed prospectively to assess the correlation between sodium excretion and health outcomes. The study concluded that "urinary sodium excretion was nonlinearly associated with all-cause mortality, such that individuals with the highest day sodium excretion was inversely associated with the cumulative incidence of ESRD, such that individuals with the lowest sodium excretion had the highest cumulative incidence of ESRD." (2) This means that both the highest and lowest levels of daily urinary sodium excretion were associated with reduced survival. The study also found that this association was independent of age, sex, duration of diabetes, the presence and severity of chronic kidney disease (CKD) (estimated glomerular filtration rate [eGFR] and log albumin excretion rate), the presence of established cardiovascular disease, and systolic blood pressure. During follow-up, 126 patients (4.5%) developed ESRD.

• Therefore, the amount of elemental sodium contained in Boliss's formulation has a small risk, which we believe is a justifiable risk to reduce the more immediate risk of ketoacidosis for a hyperglycemic person. Moreover, we believe that the long-term risks associated with higher A1C levels (for individuals not taking Boliss) are likely to be much greater than any long-term increase in the risk of heart disease that a diabetic might encounter as a result of a lifetime of using Boliss. In other words, we believe Boliss will reduce both short-term and long-term health risks. However, any concerns about an individual's health should be discussed with their healthcare provider.

  For more information, please visit: (1) http://care.diabetesjournals.org/content/34/3/703.short (2) http://care.diabetesjournals.org/content/34/3/703.short

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Boliss is designed to help reduce insulin resistance caused by dehydration and hyponatremia, and improve the effectiveness of insulin. However, it is important to note that Boliss is not a replacement for insulin or other treatments for high blood sugar. Instead, it should be used in conjunction with these treatments as prescribed by your healthcare provider.

Boliss was originally designed as an affordable and convenient product to prevent diabetic ketoacidosis (DKA) by reducing insulin resistance caused by dehydration and hyponatremia, and enhancing the speed of insulin action. However, if a patient experiences DKA, they should immediately consult with their primary care physician for appropriate treatment. It is important to note that while taking Boliss you still need to continue with your insulin and other treatments for high blood sugar.

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Yes

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Boliss is not regulated as a drug and thus is not approved by the FDA. The active ingredients in Boliss are classified as ‘generally regarded as safe” by the FDA. We plan to run a more robust clinical study in the future, with which to petition the FDA for approval.

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Boliss should be used as a rescue medication for extremely high blood sugar levels, and at most no more than four doses of up to three tablets, based on body weight, should be taken per week.

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Ask your doctor or primary care provider.

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The maximum we’d recommend is 3 tablets per day, using it no more then 3 days per week.

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We believe that the risk of rebound hyperglycemia is significantly reduced when using Boliss compared to conventional treatments such as insulin/water/wait. In conventional treatments, type 1 diabetics may self-administer additional insulin when blood sugar levels do not drop quickly enough, which can eventually lead to blood sugar levels dropping significantly below the desired level. However, we have not observed this with Boliss. Boliss causes blood sugar levels to drop rapidly, and its formulation does not independently reduce blood sugar levels. Additionally, less insulin is used when using Boliss. It's important to note that any concerns about an individual's health should be discussed with their healthcare provider.

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Boliss's patented formulation is classified as Generally Regarded as Safe (GRAS) by the FDA, which allows it to be sold as a supplement. We made the decision to market Boliss as a supplement rather than a drug for three main reasons:

1. Lower cost to the patient
2. Faster time to market
3. Simpler purchasing process (no need to check with insurance to see if it's covered)

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Boliss works by addressing the underlying causes of insulin resistance. By doing so, Boliss can be used as a supplement to traditional approaches for blood glucose management when blood sugar levels are high. It should be taken as a rescue medication whenever a diabetic reaches a high enough blood sugar level, with the level varying for each individual. To use Boliss, take 1 tablet and 8 ounces of water per 70 pounds of body weight, in addition to your current blood glucose management routine.

• Read more here