Binimetinib With Docetaxel in Treating Patients With Previously Treated, Stage IV Non-small Cell Lung Cancer

PRIMARY OBJECTIVES:

I. Evaluate the safety and tolerability of increasing doses of MEK162 (binimetinib) with
docetaxel 75 mg/m2 every 21 days in patients with stage IV non-small cell lung cancer
(NSCLC) that have progressed after at least one prior systemic therapy.

SECONDARY OBJECTIVES:

I. Determine objective tumor response rate (RR) as defined by Response Evaluation Criteria
In Solid Tumors (RECIST) 1.1 with MEK162 and standard doses of docetaxel in stage IV NSCLC.

II. Determine progression free survival (PFS) of MEK162 and standard doses of docetaxel.

III. Evaluate the pharmacokinetic profile of MEK162 when given along with docetaxel.

TERTIARY OBJECTIVES:

I. Evaluate tissue biomarkers in baseline tumors and at the time of progression to correlate
with clinical outcome II. Assess the activation status of extracellular signal-regulated
kinase (ERK), protein kinase B (Akt) and ribosomal protein S6 kinase (S6K) in tumor biopsy
samples at baseline and at the time of progression.

III. Determine the cytokine profile before and after treatment in patients.

OUTLINE: This is a dose-escalation study of binimetinib.

Patients receive binimetinib orally (PO) twice daily (BID) on days 1-21 and docetaxel
intravenously (IV) on day 21. Treatment repeats every 21 days for up to 6 courses in the
absence of disease progression or unacceptable toxicity. Patients who have stable disease or
better after completing 6 courses of binimetinib and docetaxel may continue receiving
binimetinib PO BID in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up at 30 days and then annually
for up to 5 years.

Inclusion Criteria:

- Signed written informed consent

- A histologically or cytologically confirmed diagnosis of stage IV NSCLC

- Must have progressed on at least one prior line of platinum-based therapy for stage
IV NSCLC (excluding docetaxel or mitogen activated protein kinase kinase [MEK]
inhibitors)

- Eastern Cooperative Oncology Group (ECOG) performance status 0-1

- Measurable disease defined by RECIST criteria

- Ability to provide adequate tissue from archival tumor specimen; confirmation of
adequate tissue is required prior to enrollment

- In expansion cohort only: patient's kirsten rat sarcoma viral oncogene homolog (KRAS)
mutational status must be known prior to enrollment

- Absolute neutrophil count (ANC) >= 1.5 x 10^9/L

- Hemoglobin (Hgb) >= 9 g/dL without transfusions

- Platelets (PLT) >= 100 x 10^9/L without transfusions

- Aspartate aminotransferase (AST) and/or alanine aminotransferase (ALT) =< 1.5 x upper
limit of normal (ULN)

- Total bilirubin =< 1.5 x ULN

- Creatinine =< 1.5 mg/dL

- Left ventricular ejection fraction (LVEF) >= 45% as determined by a multigated
acquisition (MUGA) scan or echocardiogram, and QTc interval =< 480ms

- Able to take and retain oral medications

- Patient is deemed by the investigator to have the initiative and means to be
compliant with the protocol (treatment and follow-up)

- Negative serum beta-human chorionic gonadotropin (HCG) test (female patient of
childbearing potential only) performed locally within 72 hours (hrs) prior to first
dose

Exclusion Criteria:

- History or current evidence of retinal vein occlusion (RVO) or current risk factors
to RVO (e.g. uncontrolled glaucoma or ocular hypertension, history of hyperviscosity
or hypercoagulability syndromes)

- History of Gilbert syndrome

- Previous or concurrent malignancy within the last 3 years with the exception of
adequately treated skin basal or squamous cell with adequate wound healing

- Prior therapy with a MEK-inhibitor or docetaxel for metastatic non-small cell lung
cancer (docetaxel in the adjuvant setting will be allowed)

- Epidermal growth factor receptor (EGFR) mutant and/or anaplastic lymphoma receptor
tyrosine kinase (ALK) gene rearranged tumor

- Impaired cardiovascular function or clinically significant cardiovascular diseases,
including any of the following within 6 months of enrollment: myocardial infarction,
unstable angina, coronary artery bypass graft (CABG), coronary angioplasty, or
stenting, symptomatic chronic heart failure, clinically significant cardiac
arrhythmias and/or conduction (except atrial fibrillation and paroxysmal
supraventricular tachycardia)

- Uncontrolled arterial hypertension despite appropriate medical therapy

- Known positive serology for human immunodeficiency virus (HIV), active hepatitis B,
and/or active hepatitis C infection

- Neuromuscular disorders that are associated with elevated creatine kinase (CK) (e.g.,
inflammatory myopathies, muscular dystrophy)

- Subjects planning on embarking on a new strenuous exercise regimen after first dose
of study treatment that can result in significant increases in plasma CK levels

- Impairment of gastrointestinal function or gastrointestinal disease (e.g., ulcerative
disease, uncontrolled nausea, vomiting, diarrhea, malabsorption)

- Any other condition that would, in the investigator's judgment, contraindicate the
patient's participation in the clinical study due to concerns regarding safety or
compliance with clinical study procedures

- Patients who have undergone major surgery =< 3 weeks prior to starting study drug or
who have not recovered from side effects of such procedure

- Pregnant or lactating women

- Women of child-bearing potential defined as all women physiologically capable of
becoming pregnant who are unwilling to use highly effective methods of contraception
throughout the study and 15 days after study drug discontinuation

- Sexually active males unless they are willing to use a condom during intercourse
while taking the drug and for 15 days after stopping treatment and are willing to
forego fathering a child in this period; a condom is required to be used also by
vasectomized men

- Medical, psychiatric, cognitive or other conditions that may compromise the patient's
ability to understand the patient information, give informed consent, comply with the
study protocol or complete the study

- Grade II or greater neuropathy at baseline

- Symptomatic brain metastases (if a patient has brain metastases and is on steroids,
the steroid dose must have been stable for at least 14 days) or brain metastases that
have not been previously treated

- Treatment with prior chemotherapy, monoclonal antibodies, other protein or peptide
therapeutics or anticancer immunotherapy within 21 days of the first dose of study
drug

- Treatment with prior radiotherapy within 28 days of initiating study drug; however,
if the radiation portal covered =< 10% of the bone marrow reserve, the patient may be
enrolled without respect to the end date of radiotherapy