3 Month PHI PAD PoM Study

This is a multi-center, randomized, blinded, placebo controlled study to evaluate the safety
of GSK1278863 and its acute and short-term (e.g. 14d) effects on calf muscle endurance and
walking ability in subjects with PAD and symptomatic claudication. Functional assessments
will be performed following a single high dose (300mg), a single low dose (15mg), and
following 14 days of low dose treatment (15mg q.d.). The objectives of this study are to: 1)
Evaluate the safety and tolerability of GSK1278863 administered as a single dose and as
sub-chronic low dosing (i.e. 14 days) in subjects with peripheral artery disease; 2) To
demonstrate the potential pharmacodynamic effect of GSK1278863 on functional measures of calf
muscle endurance and fatigability and timed walking distance following a single high or low
dose and after 14 days of multiple low dose administration in subjects with
claudication-limited peripheral artery disease. In this hypothesis-generating study, multiple
assessments of ambulatory and skeletal muscle function will be made during standardized tests
of claudication-limited exercise performance, and 3). Characterize the relationship, if any,
between the doses and plasma concentrations of GSK1278863 and the pharmacodynamic effects.

Inclusion Criteria:

- Subjects ≥ 40 years of age.

- Male subjects must use one of the contraceptive methods listed in Section 8.1 for 90
days post-last dose.

- Females must be postmenopausal, surgically sterilized, or practicing a suitable method
of birth control so that in the opinion of the investigator they will not become
pregnant during the course of the study.

A female subject is eligible to participate if she is of child-bearing potential and agrees
to use one of the contraception methods listed in Section 8.1 for an appropriate period of
time (as determined by the product label or investigator) prior to the start of dosing to
sufficiently minimize the risk of pregnancy at that point. Female subjects must agree to
use contraception until 30 days post-last dose.

- Peripheral artery disease defined as an ankle-brachial index (ABI) at rest ≤ 0.90 in
at least one leg in which the patient experiences claudication. For all subsequent
evaluations, the Index Leg refers to the symptomatic leg with the lowest ABI.

- Claudication symptoms with stable severity for at least 3 months prior to screening.

- The patient is able to provide written informed consent to participate in this study.

- AST and ALT < 2xULN; alkaline phosphatase and bilirubin greater than or equal too
1.5xULN (isolated bilirubin >1.5xULN is acceptable if bilirubin is fractionated and
direct bilirubin <35%).

- Confirmed QTcB or QTcF < 450 msec; or QTc < 480 msec in subjects with bundle branch
block.

- Subjects must be able to perform performance/exercise testing

Exclusion Criteria:

- Coronary artery bypass graft (CABG), open peripheral vascular procedures, or major
surgical procedures within 6 months prior to screening or patients likely to require
revascularization during the course of the trial. Endovascular procedures within 3
months prior to screening.

- Any unstable vascular syndromes (such as TIA, CVA, unstable angina or acute MI),
including major changes to related medications, within 6 months prior to
randomization.

- Critical leg ischemia classified as Fontaine Stage III-IV (rest pain, tissue necrosis
or gangrene).

- Pregnant or nursing women (women capable of childbearing must have a negative
pregnancy test).

- A hemoglobin value at screening is:

Male subjects or post-menopausal females: > 15.5 g/dL Female subjects: > 14.5 g/dL

- Active malignancy or diagnosis of malignancy within 5 years prior to screening
(excluding successfully treated basal or squamous cell carcinoma).

- Other clinically significant cardiovascular, pulmonary, renal, endocrine, hepatic,
neurological, psychiatric, immunological, gastrointestinal, hematological, or
metabolic disease that is, in the opinion of the Investigator or the Medical Monitor,
not stabilized or may otherwise confound the results of the study.

- Patients with a baseline medical history of proliferative diabetic retinopathy,
preproliferative diabetic retinopathy, or wet age-related macular degeneration (AMD)

- Previously enrolled in a gene therapy clinical study unless patient was randomized to
placebo.

- Plans to initiate a formal exercise training program during the course of the study,
or initiation of a formal exercise training program within 3 months prior to
screening.

- Poorly controlled hypertension (defined as seated resting BP >160 mmHg systolic or >
95 mmHg diastolic, or both).

- Hypotension (defined as seated resting BP < 95 mmHg systolic or < 55 mmHg diastolic,
or both, or symptomatic hypotension [seated, supine, or orthostatic]).

- Exercise tolerance, including bilateral heel raise and Six-Minute Walk Test
performance, that is limited by co-morbid conditions or diseases other than
claudication.

- Poorly controlled diabetes defined as Hemoglobin A1c (HbA1c) > 10%.

- Creatinine > 2.5 mg/dL or undergoing hemodialysis.

- Thrombocytopenia defined as platelet count < 100,000/mm3 at screening.

- Hematocrit ≤ 30% or ≥ 55%.

- International Normalized Ratio (INR) > 1.5.

- A positive Hepatitis B surface antigen or positive Hepatitis C antibody result if
performed within 3 months of screening (testing not required at Screening).

- History of alcohol or drug abuse, or a significant medical or psychiatric disorder
that may impair compliance with the requirements of the protocol.

- The patient has received an investigational drug within 30 days prior to this study.

- The patient is enrolled or plans to enroll in another clinical trial during this study

- History of venous thrombosis, defined as deep vein thrombosis, pulmonary embolism or
other venous thrombotic condition, within 1 year prior to Screening.

- Acute peptic ulcer disease or history of chronic rectal bleeding.

- Patients with a pre-existing condition interfering with normal gastrointestinal
anatomy or motility, and/or hepatic function that could interfere with the absorption,
metabolism, and/or excretion of the study drugs. Examples of conditions that could
interfere with normal gastrointestinal anatomy or motility include gastrointestinal
bypass surgery, partial or total gastrectomy, small bowel resection, vagotomy,
malabsorption, Crohn's disease, ulcerative colitis, or celiac sprue.

- Use of prescription drugs within 7 days prior to first dose of study drug (Day 1)
until after completion of all study drug doses and Day 35 assessments:

which are known to be inhibitors of CYP 2C8 OR which are known to be both CYP 2C8 and
OATP1B1 substrates OR which rely mainly on OATP1B1/1B3 for hepatic clearance as described
in Section 9 of the protocol.

- Use of prescription drugs within 14 days prior to first dose of study drug (Day 1)
until completion of all study drug doses and Day 35 assessments, which are known to be
inducers of CYP 2C8, as described in Section 9 of the protocol.

- Use of non-prescription drugs, including vitamins, herbal and dietary supplements
(including St John's Wort) within 7 days (or 14 days if the drug is a potential enzyme
inducer) or 5 half-lives (whichever is longer) prior to the first dose of study drug
(Day 1) through the Follow-up Visit (Day 65), unless, in the opinion of the
Investigator, medication will not interfere with the study procedures or compromise
subject safety and GSK Medical Monitor concurs.

- History of sensitivity to any of the study drugs, or components thereof, or a history
of drug or other allergy that, in the opinion of the investigator or GSK Medical
Monitor, contraindicates their participation.

- Patient is mentally or legally incapacitated.