Safety, Pharmacokinetics (PK) of AKT and MEK Combination

Inclusion Criteria:

Part 1 - Dose Escalation

Subjects eligible for enrollment in the study must meet all of the following criteria:

Male or female 18 years or older, at the time of signing the informed consent.

Capable of giving written informed consent, which includes compliance with the
requirements and restrictions listed in the consent form.

Histologically or cytologically-confirmed diagnosis of solid tumor malignancy that is not
responsive to standard therapies or for which there is no approved or curative therapy or
for subjects who refuse standard therapy (Part 1A). Part 1B subjects must have a confirmed
diagnosis of one of the following (documented lab results confirming mutational status
must be available at Screening):

colorectal cancer (CRC): KRAS mutation non-small cell lung (NSCLC): KRAS mutation
Pancreatic: no mutational status specified Endometrial: no mutational status specified
Ovarian: no mutational status specified Squamous cell carcinoma of the head and neck: no
mutational status specified BRAF wild type melanoma (preferentially enrolled to Part 2)
BRAF inhibitor failure melanoma. This includes BRAF-mutant melanoma that is either
initially refractory to BRAF-inhibitor therapy OR that Initially responds to
BRAF-inhibitor therapy but eventually develops documented radiographic progression to a
BRAF inhibitor while on therapy Triple negative breast cancer (TNBC) (preferentially
enrolled to Part 2) NOTE: Subjects who do not meet one of the categories described above
but who have molecular evidence suggesting benefit from the study drugs may be considered
for enrollment after discussion with the GlaxoSmithKline (GSK) Medical Monitor.

Performance Status score of 0 or 1 according to the Eastern Cooperative Oncology Group
(ECOG) scale.

Able to swallow and retain oral medication.

Must agree to collection of blood samples for the evaluation of circulating free DNA
(cfDNA) (Part 1B or Part 2).

A female subject is eligible to participate if she is of:

Non-childbearing potential defined as pre-menopausal females with a documented tubal
ligation or hysterectomy; or postmenopausal defined as 12 months of spontaneous amenorrhea
(in questionable cases a blood sample with simultaneous follicle stimulating hormone [FSH]
greater than 40 MlU/ml and estradiol less than 40 pg/ml [less than 140 pmol/L] is
confirmatory). Females on hormone replacement therapy [HRT] and whose menopausal status is
in doubt will be required to use one of the contraception methods in Section 8.1.1 if they
wish to continue their HRT during the study. Otherwise, they must discontinue HRT to allow
confirmation of post-menopausal status prior to study enrollment. For most forms of HRT,
at least 2 to 4 weeks will elapse between the cessation of therapy and the blood draw;
this interval depends on the type and dosage of HRT. Following confirmation of their
post-menopausal status, they can resume use of HRT during the study without use of a
contraceptive method.

Child-bearing potential and agrees to use one of the contraception methods listed in
Section 7.3.2 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. Additionally, women of child-bearing potential must have a negative serum
pregnancy test within 14 days prior to the first dose of study medication. Female subjects
must agree to use contraception until four weeks after the last dose of study medication.

Note: Oral contraceptives are not reliable due to potential drug-drug interaction and
should only be used in combination with the alternative methods outlined in Section 8.1.1.

Male subjects must agree to use one of the contraception methods listed in Section 8.1.2.
This criterion must be followed from the time of the first dose of study medication until
four months after the last dose of study medication.

Adequate organ system function as defined in protocol. Absolute neutrophil count (ANC)
greater than or equal to 1.5 X 10 to the ninth/L Hemoglobin greater than or equal to 9.5
g/dL Platelets greater than or equal to 75 X 10 to the ninth/L Prothrombin time (PT) /
International Normalized Ratio (INR) and Partial Thromboplastin Time (PTT) less than or
equal to 1.1 X ULN Total bilirubin less than or equal to 1.5 x ULN (isolated bilirubin
greater than 1.5 x ULN is acceptable if bilirubin is fractionated and direct bilirubin
less than 35 percent) AST and ALT less than or equal to 1.5 X ULN Albumin greater than 2.5
g/dL Creatinine less than or equal to ULN OR Calculated creatinine clearance greater than
or equal to 30 mL/min OR 24-hour urine creatinine clearance greater than or equal to 30
mL/min

Fasting Serum Glucose les than 126mg/dL Cardiac Ejection fraction greater than or equal to
lower limit of normal (LLN) by ECHO

Inclusion Criteria for Part 2 - Expansion Cohort:

Histologically- or cytologically-confirmed diagnosis of one of the following:

Triple negative (estrogen receptor(ER)-/ progesterone receptor(PR)-/ human epidermal
growth factor receptor 2 (HER2)) breast cancer in the locally advanced or metastatic
setting BRAF-wild type melanoma. Based on emerging data, subjects with these tumor
histologies may be required to meet specific genetic selection criteria if those criteria
are felt to improve the likelihood that a given subject will respond to study drug(s). If
this is to occur, the site and the Investigational Review Board (IRB) will be notified but
this change will not constitute a protocol amendment.

Known Phosphatase and tensin homolog (PTEN) status of tumor. At least 6 of the subjects
enrolled in Stage 1 with each tumor type will have PTEN deficiency while at least 6 others
will be PTEN wild type.

If the subject's tumor PTEN status was previously determined by an acceptable,
analytically validated assay (i.e., Immunohistochemistry (IHC), fluorescence in situ
hybridization (FISH), sequencing, copy number analysis) then PTEN by IHC at Screening will
not need to be repeated for the purpose of enrollment in this study. However, archival
tumor tissue or tissue from a fresh biopsy specimen should be submitted for confirmation
of PTEN status by a central laboratory using IHC.

If PTEN status was not previously determined, archival tissue from a previous tumor biopsy
specimen must be available for PTEN IHC analysis; if archival tissue is not available or
found to not contain tumor tissue, a fresh biopsy is required to obtain tumor tissue for
testing.

Subjects in Part 2 that have been previously diagnosed with Type 2 diabetes must also meet
the additional following criteria:

Diagnosis of diabetes greater than or equal to 6 months prior to enrolment HbA1C less than
or equal to 8 percent at Screening visit

Exclusion Criteria

Subjects meeting any of the following criteria must not be enrolled in the study:

Chemotherapy, radiotherapy, immunotherapy, or other anti-cancer therapy including
investigational drugs within 28 days or 5 half lives, whichever is shorter prior to the
first dose of any one of the investigational drugs described in this study. Prior exposure
to either a MEK inhibitor or an AKT inhibitor is not permitted.

Current use of a prohibited medication or requires any of these medications during
treatment with the study treatments.

Unresolved toxicity greater than National Cancer Institute (NCI) Common Terminology
Criteria for Adverse Events (CTCAE), version 4.0 (NCI-CTCAE v4) Grade 1 from previous
anti-cancer therapy unless agreed to by a GSK Medical Monitor and the Investigator, and
where a GSK Medical Monitor and the investigator consider that the ongoing toxicity will
not introduce additional risk factors and will not interfere with the study procedures.

Presence of active gastrointestinal (GI) disease or other condition that could affect
gastrointestinal absorption (e.g. malabsorption syndrome) or predispose a subject to GI
ulceration. Subjects with prior Whipple procedure are eligible.

Evidence of mucosal or internal bleeding.

Any major surgery within the last four weeks.

Previously diagnosed with Type 1 diabetes mellitus.

Previously diagnosed with Type 2 diabetes (Part 1A or Part 1B ONLY). Subjects with a
history of steroid-induced hyperglycemia may be enrolled.

Any malignancy related to human immunodeficiency virus (HIV), history of HIV, history of
known hepatitis B virus (HBV) surface antigen positivity (subjects with documented
laboratory evidence of HBV clearance may be enrolled) or positive hepatitis C virus (HCV)
antibody.

Known active infection requiring parenteral or oral anti-infective treatment.

Subjects with leptomeningeal disease.

Subjects with brain metastases are excluded if their brain metastases are:

Symptomatic Treated (e.g., surgery, radiation therapy) but not clinically and
radiographically stable one month after therapy (as assessed by at least two distinct
contrast enhanced magnetic resonance imaging (MRI) or computerized axial tomography (CT)
scans over at least a one month period), OR Asymptomatic and untreated but greater than 1
cm in the longest dimension Subjects with small (less than or equal to 1 cm in the longest
dimension), asymptomatic brain metastases that do not need immediate therapy can be
enrolled. Subjects must also be off of enzyme-inducing anticonvulsants for more than 4
weeks.

Part 1B: Subjects with brain metastases who have been off corticosteroids for at least 2
months can be enrolled.

Part 2 (A or B): Subjects with brain metastases on a stable (i.e., unchanged) dose of
corticosteroids for more than one month, or those who have been off corticosteroids for at
least 2 weeks can be enrolled.

QTcF interval greater than or equal to 480 milliseconds (msecs) (greater than or equal to
500 msec for subject with bundle branch block).

History or evidence of current clinically significant uncontrolled arrhythmias. Subjects
with controlled atrial fibrillation for greater than 1 month prior to study Day 1 are
eligible.

History of acute coronary syndromes (including unstable angina), myocardial infarction,
coronary angioplasty, or stenting or bypass grafting within six months of Screening.

Class II, III, or IV heart failure as defined by the New York Heart Association (NYHA)
functional classification system.

Other clinically significant electrocardiography (ECG) abnormalities including 2nd degree
(Type II) or 3rd degree atrioventricular (AV) block.

Subject with intra-cardiac defibrillators or pacemaker.

Presence of cardiac metastases.

Any serious or unstable pre-existing medical, psychiatric, or other condition (including
lab abnormalities) that could interfere with subject's safety or providing informed
consent.

Known immediate or delayed hypersensitivity to any of the components of the study
treatment(s).

Evidence of severe or uncontrolled systemic diseases (e.g., unstable or uncompensated
respiratory, hepatic, renal, or cardiac disease, including unstable hypertension).

Pregnant or lactating females.

History or current evidence / risk of retinal vein occlusion (RVO) or central serous
retinopathy (CSR):

History of RVO or CSR, or the presence of predisposing factors to RVO or CSR at the time
of screening (e.g., uncontrolled glaucoma or ocular hypertension, uncontrolled systemic
disease such as hypertension, diabetes mellitus, or history of hyperviscosity or
hypercoagulability syndromes).

Visible retinal pathology as assessed by ophthalmic exam that is considered a risk factor
for RVO or CSR such as:

Evidence of new optic disc cupping Evidence of new visual field defects Intraocular
pressure greater than 21 mm Hg as measured by tonography