Pharmacokinetic Study of Diazoxide Choline in Hypertriglyeridemic Subjects

A Multiple-Dose Pharmacokinetic Study of Diazoxide Choline Controlled-Release Tablet (DCCR) in Subjects With Elevated Fasting Triglyceride Levels

Once a day oral administration with DCCR is the optimal dosing regimen

POPULATION The population will consist of generally healthy subjects with elevated fasting triglyceride levels in the range of ≥ 150 mg/dL and ≤ 1500 mg/dL at the Screening Visit.

Number of Subjects A total of 10 subjects will be enrolled in the study at 1 site in the USA.

Inclusion Criteria:

Basic requirements

1. Healthy male and female subjects 18 to 75 years of age, inclusive at the time of dosing

2. Body mass index (BMI) between 22 and 35 kg/m2

   Specific laboratory test results

3. Fasting triglyceride ≥ 150 mg/dL and ≤ 1500 mg/dL

4. Fasting glucose ≤ 110 mg/dL

5. HbA1c ≤ 6.0 %

Exclusion Criteria:

Medications: recent, current, anticipated

1. Thyroid hormones or preparations within 1 month prior to Screening Visit (except in subjects on stable dose of replacement therapy for at least 1 month)

2. Thiazide diuretics within 2 weeks prior to Screening Visit

   History of allergic reaction or significant intolerance to:

3. Diazoxide

4. Thiazides

5. Sulfonamides

   Lifestyle changes

6. Subjects intending to change exercise habits, and/or quit smoking

   Specific diagnoses, medical conditions and history

7. Known type I or III hyperlipidemia

8. Known type 1 DM

9. Known type 2 DM

10. Any other clinically significant endocrine, cardiovascular, pulmonary, neurological, psychiatric, hepatic, gastrointestinal, hematological, renal, or dermatological disease interfering with the assessments of the investigational drug, according to the Investigator

    Specific laboratory test results

11. Any relevant biochemical abnormality interfering with the assessments of the investigational drug