Pharmacokinetic Study of CYCLOSET ® 0.8 mg Tablets in Children and Adolescent Type 2 Diabetes Mellitus Subjects

The study is a multi-center, single dose, open-label, 1-period design. Thirty (30) patients
will be enrolled in the study and at least twenty-four (24) patients are expected to
complete the study.

Male and female patients with confirmed Type 2 Diabetes, non-or ex-smokers, aged 10 to less
than 18 years will be selected according to the inclusion and exclusion criteria.

Patients will be admitted to the clinical site at least 10 hours prior to drug
administration which will occur within 2 hours of waking on the morning of Day 2.

Ondansetron hydrochloride will be administered orally, approximately 6 hours before the
dosing time of Cycloset (bromocriptine mesylate). Subjects weighing 50 to 60 kg will receive
6mg ondansetron hydrochloride (liquid 7.5 ml) and subjects weighing ≥60 kg will receive
ondansetron hydrochloride 8 mg (liquid 10 ml).

A single, weight-adjusted dose of CYCLOSET (bromocriptine mesylate), of approximately 0.048
mg/kg, will be administered orally with 240 mL of water in the morning, after a 10-hour
overnight fast, and thirty minutes after the start of a standardized breakfast that meets
American Diabetes Association diet recommendations.

On day 2, after a supervised overnight fast, the patients will be awakened, vital signs
(blood pressure, pulse rate and body temperature) will be measured and the first blood
sample (T= 0) will be collected.

Seventeen (17) blood samples will be collected for pharmacokinetic sampling at 0.25, 0.50,
0.75, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 10, 12, 16, 24 and 36 hours post drug administration.

Finger sticks for blood glucose levels will be obtained every hour for the first 4 hours
following administration of bromocriptine mesylate, and then additionally as deemed
necessary by the study physician.

Safety will be evaluated through the assessment of adverse events and laboratory tests and
vital signs.

Inclusion Criteria:

- Availability for entire study and willingness to adhere to protocol requirements as
evidenced by (ICF) duly read, signed and dated by the patient and responsible parent
or guardian

- Positive diagnosis of T2DM according to ADA criteria. There is no requirement for
time since diagnosis as long as ADA guidelines have been followed.

- Aged at least 10 years but less than 18 years at time of enrollment

- BMI greater than 80th percentile for age and sex and body weight equal to or greater
than 50 kg

- Clinical laboratory values within the laboratory's stated normal range - if not
within this range, they must be without any clinical significance

- Healthy according to the medical history, laboratory results and physical examination

- Non- or ex-smokers (defined as someone who completely stopped smoking for at least 30
days before day 1 of this study).

Exclusion Criteria:

- Evidence to indicate a diagnosis of Type 1 diabetes

- Body weight less than 50 kilograms

- Systolic blood pressure lower than 115mmHg or diastolic blood pressure lower than 68
mmHg

- Significant history of hypersensitivity to bromocriptine mesylate, ondansetron, other
ergot alkaloids or any related products, including excipients of the formulation as
well as severe hypersensitivity reactions (like angioedema) to any drugs

- Presence of significant gastrointestinal, liver or kidney disease, or any other
conditions known to interfere with the absorption, distribution, metabolism or
excretion of drugs or known to potentiate or predispose to undesired effects

- Serum aspartate aminotransferase (AST) greater than 3X ULN, and/or serum alanine
aminotransferase (ALT) greater than 3X ULN, and/or serum total bilirubin greater than
2.0 mg/dL.

- Calculated glomerular filtration rate less than 80 mL/min based on the Schwartz
Formula

- Presence or history of uncontrolled hypertension: systolic pressure greater than 145
mmHg and/or diastolic pressure greater than 95 mmHg, hypertensive disorders of
pregnancy, hypertension post-partum and in the puerperium

- History of surgery that may affect drug bioavailability, including but not limited to
cholecystectomy

- Presence of significant cardiovascular, pulmonary, hematologic, neurologic,
psychiatric, endocrine, immunologic or dermatologic disease

- Symptoms and/or history of serious psychiatric or psychotic disorders

- Presence of significant heart disease or disorder according to ECG

- Presence of malignancy, particularly pituitary gland malignancy and prolactinoma

- Presence or history of migraine headache or syncope

- Pregnant according to a positive serum pregnancy test or lactating

- Females less then four months post-partum

- Current history of illicit drug dependency, use or alcohol abuse (greater than 3
units of alcohol per day, intake of excessive alcohol, acute or chronic).

- Use of drugs for the treatment of ADD and ADHD

- Inhaled corticosteroid use other than as a rescue treatment in case of asthma attack.
Use of oral glucocorticoids. Use of oral steroids within the 60 days prior to study
entry.

- Any clinically significant illness in the previous 28 days before day 1 of this study

- Use of any cytochrome P450 (CYP) 3A4 enzyme-modifying drugs, including strong
inhibitors of CYP 3A4 enzymes and strong inducers of CYP3A4 enzymes (such as
barbiturates, carbamazepine, phenytoin and rifampin), in the previous 28 days before
Day 1 of this study

- Participation in another clinical trial or donation of 50 mL or more of blood in the
previous 42 days before day 1 of this study

- Donation of 500 mL or more of blood in the previous 56 days before Day 1 of this
study, as well as donation in excess of 900 mL of blood over the previous 20 weeks

- Positive urine screening of drugs of abuse

- Positive results to HIV, HBsAg or anti-HCV tests