Regorafenib and Methotrexate in Treating Participants With Recurrent or Metastatic KRAS Mutated Non-Small Cell Lung Cancer

PRIMARY OBJECTIVES:

I. To determine the progression free survival (PFS) of the combination of regorafenib and
methotrexate for metastatic KRAS mutated non-small cell lung cancer (NSCLC) patients who have
received at least 1 prior systemic therapy.

SECONDARY OBJECTIVES:

I. To determine the objective response rate (ORR) of the combination of regorafenib and
methotrexate for metastatic KRAS mutated NSCLC patients who have received at least 1 prior
systemic therapy.

II. To determine the disease control rate (DCR) at 8 weeks of the combination of regorafenib
and methotrexate for metastatic KRAS mutated NSCLC patients who have received at least 1
prior systemic therapy.

III. To determine the safety of the combination of regorafenib and methotrexate in metastatic
KRAS mutated NSCLC patients who have received at least 1 prior systemic therapy, assessed as
the number of subjects that experience a treatment-emergent adverse event.

IV. To determine the safety of the combination of regorafenib and methotrexate in metastatic
KRAS-mutated NSCLC patients who have received at least 1 prior systemic therapy, assessed as
the number (percent) of participants experiencing any dose-limiting toxicity (DLT).

V. To determine the pharmacokinetic parameters of methotrexate when combined with regorafenib
(i.e., trough and maximum serum concentration [Cmax]).

OUTLINE:

Participants receive regorafenib orally (PO) once daily (QD) and methotrexate PO twice weekly
with 2-3 days apart on a 3 week on / 1 week off schedule. Courses repeat every 28 days in the
absence of disease progression or unacceptable toxicity.

After completion of study treatment, participants will come in for an end of study treatment
visit.

Inclusion Criteria:

- Histologic or cytologic confirmed diagnosis of recurrent or metastatic non-squamous
non-small cell lung cancer

- Documentation of pathogenic KRAS mutation

- Previous receipt of at least one systemic therapy for recurrent or metastatic disease
OR previous receipt of adjuvant systemic therapy within 6 months of enrollment; there
is no limit on number of prior therapies allowed

- Prior systemic therapy must be completed within 2 weeks of study treatment, with
either improvement of clinically significant treatment-related toxicities to grade 0-1
OR stabilized to a new baseline

- Previously treated OR asymptomatic non-progressing < 1 cm untreated brain metastases
are allowed

- Measurable disease based on Response Evaluation Criteria in Solid Tumors (RECIST)
version 1.1 criteria

- Ability to understand and the willingness to sign a written informed consent document

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

- Absolute neutrophil count (ANC) ≥ 1500/mm^3

- Platelet count ≥ 100,000 /mm^3

- Hemoglobin (Hb) ≥ 9 g/dL

- Serum creatinine ≤ 1.5x upper limit of normal (ULN) OR calculated (Cockcroft Gault
formula) or measured creatinine clearance ≥ 50 mL/min for patients with creatinine
levels > 1.5x ULN

- Total bilirubin ≤ 1.5x ULN OR direct bilirubin ≤ ULN for patients with total bilirubin
levels > 1.5x ULN

- Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 3x ULN (≤ 5x ULN
for patients with liver involvement of their cancer)

- Must be able to swallow and retain oral medication

- Women patients of childbearing potential and men patients with women partners of
childbearing potential must agree to use adequate contraception or agree to abstain
from heterosexual activity beginning at the time of signing informed consent until at
least 3 months after the last dose of study treatment; post-menopausal women (defined
as no menses for at least 1 year) and surgically sterilized women are not considered
childbearing

Exclusion Criteria:

- Previously treated with regorafenib

- Known allergy to regorafenib or methotrexate

- Currently receiving another systemic standard or investigational anti-cancer therapy;
prior investigational therapy must be completed within 4 half-lives (if known) or 2
weeks, whichever is longer; the maximal washout of investigational therapy will not
exceed 4 weeks prior to study treatment; bone medications such as bisphosphonates and
receptor activator of nuclear factor kappa-Β (RANK) ligand inhibitors permitted

- Leptomeningeal disease as documented by cerebrospinal fluid (CSF) cytology

- Clinically significant cardiovascular related disease including:

- Uncontrolled hypertension (systolic pressure > 140 mm Hg or diastolic pressure >
90 mmHg on repeated measurements, i.e., 3 or more separate days within one week)
despite optimal medical management

- Congestive heart failure - New York Heart Association (NYHA) class III or greater

- Active coronary artery disease (i.e., unstable or new onset angina within 3
months of study treatment; myocardial infarction within 6 months of study
treatment)

- Clinically significant cardiac arrhythmias other than atrial flutter/fibrillation

- Stroke, including transient ischemic attacks, within 6 months of study treatment

- Other clinically significant arterial events, except for controlled asymptomatic
pulmonary embolism, within 6 months of study treatment

- Clinically significant hemorrhage or bleeding event within 1 month of study treatment

- Uncontrolled symptomatic pleural effusion or ascites

- Known active additional malignancy that is undergoing or expected to undergo systemic
treatment during duration of study participation

- Known history of human immunodeficiency virus (HIV) infection or known current active
hepatitis B (i.e., hepatitis [Hep] B deoxyribonucleic acid [DNA] positive in prior 3
months) or hepatitis C infection (i.e., Hep C ribonucleic acid [RNA] positive in prior
3 months)

- Major surgical procedure (e.g., involving the opening of a major body cavity) within 4
weeks of study treatment; this does not apply to low risk procedures (i.e.,
thoracentesis; paracentesis; chest tube / PleurX catheter placement; line placement;
needle biopsy of tumor; and bronchoscopy)

- Presence of a clinically significant non-healing wound, non-healing ulcer, or bone
fracture

- Concomitant therapy required at time of first dose of study treatment, including:

- Strong CYP3A4 inhibitors and CYP3A4 inducers

- Regular use of nonsteroidal anti-inflammatory drugs (NSAIDs), proton pump
inhibitors, and probenecid

- Women who are pregnant or breast feeding

- Any condition which, in the investigator's opinion, including substance abuse,
medical, psychological or social conditions that makes the patient unsuitable for
trial participation or may interfere with the patient's participation in the study