Does Dapagliflozin Provide Additional Health Benefits To Dietary Counseling For Weight Loss?

This is a randomized, prospective, placebo-controlled, double blind, repeated measures study.
50 overweight/obese adults (body mas index > 27.5 kg/m2) will be recruited for participation
and randomly assigned to one of two 12 week treatments: (1) daily oral administration of
Dapagliflozin with dietary counseling to promote weight loss; or, (2) daily oral
administration of a placebo with dietary counseling to promote weight loss.

Inclusion Criteria:

- Provision of informed consent prior to any study specific procedures.

- Aged 18-65 years.

- No known Type 2 Diabetes

- Body mass index greater than or equal to 27.5 kg/m^2

- Limited exercise participation (maximum of 3/week regularly scheduled activity
sessions of < 30 minutes during the previous month).

- Completion of a screening visit consisting of medical history, physical examination,
and 12-lead electrocardiogram and blood pressure assessment at rest and during
incremental exercise to volitional exhaustion (Note: Subjects with abnormal screening
values may be eligible if the results are not clinically significant, as judged by the
investigator or medical monitor)

- Agree to abide by the study schedule and dietary restrictions and to return for the
required assessments

- Women of childbearing potential must have negative pregnancy test and be using
acceptable contraception

Exclusion Criteria:

- Evidence of clinically significant cardiovascular, respiratory, renal, hepatic,
pulmonary, gastrointestinal, haematological, neurological, psychiatric, or other
disease that may interfere with the objectives of the study or the safety of the
subject, as judged by the investigator in agreement with the sponsor or medical
monitor, have been hospitalized in the past 2 years as a result of these conditions,
or are receiving pharmacological treatment for these conditions.

- Use of prescription drugs (see exceptions listed below) or herbal preparations in the
2 weeks before study commencement. Prior use of medication or herbal preparations in
the 4 weeks before study commencement that are intended for weight-loss and/or
sold/marketed as weight-loss products or may alter metabolism. Permitted Prescription
Drugs: Birth Control, Less than a 7 day short course of antibiotics. Note: Rifampicin
is not permitted. Other medicines, such as those for gastroesophageal reflux disease,
depression, and Over The Counter analgesics and allergy medications,may be allowed,
but will be approved on a case-by-case basis.

- Is currently enrolled in another clinical study for another investigational drug or
has taken any other investigational drug within 30 days before the screening visit.

- Habitual and/or recent use (within 2 years) of tobacco.

- Being considered unsuitable for participation in this trial for any reason, as judged
by the investigator or medical monitor.

- History of serious hypersensitivity reaction to Dapagliflozin.

- Severe renal impairment, end-stage renal disease, or dialysis.

- Pregnant or breastfeeding individual.

- Severe hepatic insufficiency and/or significant abnormal liver function defined as
aspartate aminotransferase (AST) >3x upper limit of normal and/or alanine
aminotransferase (ALT) >3x upper limit of normal.

- Total bilirubin >2.0 mg/dL (34.2 umol/L).

- Positive serologic evidence of current infectious liver disease including Hepatitis B
viral antibody immunoglobulin M, Hepatitis B surface antigen and Hepatitis C virus
antibody.

- Estimated Glomerular Filtration Rate <60 mL/min/1.73 m^2 (calculated by
Cockcroft-Gault formula).

- History of bladder cancer.

- Recent cardiovascular events in a patient, including any of the following: acute
coronary syndrome within 2 months prior to enrolment; hospitalization for unstable
angina or acute myocardial infarction within 2 months prior to enrolment; acute stroke
or trans-ischemic attack within two months prior to enrolment; less than two months
post coronary artery revascularization; congestive heart failure defined as New York
Heart Association class IV, unstable or acute congestive heart failure. Note: eligible
patients with congestive heart failure, especially those who are on diuretic therapy,
should have careful monitoring of their volume status throughout the study.

- Blood pressure at enrolment: Systolic blood pressure ≥160 mmHg and/or diastolic blood
pressure ≥100 mmHg.

- Blood pressure at randomization: Systolic blood pressure ≥165 mmHg and/or diastolic
blood pressure ≥100 mmHg

- Individuals who, in the judgment of the medical monitor, may be at risk for
dehydration.

- Individuals with a history of fragility fracture, or bone mineral density values
reflective of risk for fracture (DEXA Z-score men <50, and T-score