A Study of Nivolumab In Combination With Cabozantinib in Patients With Non-Clear Cell Renal Cell Carcinoma

Inclusion Criteria:

- Signed and dated IRB-approved Informed Consent Form

- Pathologic or histologically confirmed unresectable advanced or metastatic nccRCC

- 0 or 1 prior systemic therapies, including treatment in the adjuvant setting

- Availability of a representative formalin fixed, paraffin embedded tumor specimen or
fresh frozen tissue specimen that enables the definitive diagnosis of RCC, accompanied
by an associated pathology report. Specimens can be collected by surgical resection or
biopsy of the primary tumor or biopsy or resection of a metastatic lesion.

- Measurable disease, as defined by RECIST 1.1

- Age ≥18 years

- KPS ≥ 70

- Recovery to baseline or ≤ Grade 1 CTCAE v4 from toxicities related to any prior
treatments, unless adverse events (AE(s)) are clinically nonsignificant and/or stable
on supportive therapy.

- Adequate hematologic and end organ function, defined by the following laboratory
results obtained within 14 days prior to the first study treatment:

- ANC ≥ 1500 cells/μL (without granulocyte colony stimulating factor support within
2 weeks prior to Cycle 1, Day 1)

- WBC counts ≥ 2500/μL and ≤ 15,000/μL without G-CSF

- Lymphocyte count ≥ 500/μL

- Platelet count ≥100,000/μL (without transfusion within 2 weeks prior to Cycle 1,
Day 1)

- Hemoglobin ≥9.0 g/dL

- Alanine aminotransferase (ALT), aspartate aminotransferase (AST), and alkaline
phosphatase (ALP) ≤ 3 x upper limit of normal (ULN). ALP ≤ 5 x ULN with documented
bone metastases.

- Serum bilirubin ≤ 1.5 x ULN

- Serum albumin ≥ 2.8 g/dl

- Patients with known Gilbert disease who have serum bilirubin level ≤ 3 x ULN may be
enrolled.

- INR and aPTT ≤ 1.5 x ULN • This applies only to patients who are not receiving
therapeutic anticoagulation; patients receiving therapeutic anticoagulation should be
on a stable dose.

- Creatinine ≤ 2.0 x ULN or Calculated Creatinine clearance ≥ 30mL/min

- For women who are not postmenopausal (12 months of amenorrhea) or surgically sterile
(absence of ovaries and/or uterus): agreement to use two adequate methods of
contraception, including at least one method with a failure rate of ≥ 1% per year

- Urine protein/creatinine ratio (UPCR) ≤ 1 mg/mg (≤ 113.2 mg/mmol)

- Sexually active fertile subjects and their partners must agree to use medically
accepted methods of contraception (eg, barrier methods, including male condom, female
condom, or diaphragm with spermicidal gel) during the course of the study and for 5
months after the last dose of study treatment for females and 7 months for males.

- Female subjects of childbearing potential must not be pregnant at screening. Females
of childbearing potential are defined as premenopausal females capable of becoming
pregnant (ie, females who have had any evidence of menses in the past 12 months, with
the exception of those who had prior hysterectomy).

However, women who have been amenorrheic for 12 or more months are still considered to be
of childbearing potential if the amenorrhea is possibly due to prior chemotherapy,
antiestrogens, low body weight, ovarian suppression or other reasons.

- Capable of understanding and complying with the protocol requirements and must have
signed the informed consent document.

Exclusion Criteria:

- Prior treatment with an immunotherapy agent including high dose IL-2, anti-CTLA-4,
anti-PD1, and anti-PD-L1 agents

- Prior treatment with cabozantinib for non-clear cell RCC

- Receipt of any type of small molecule kinase inhibitor within 2 weeks of treatment.

- Receipt of any type of anti-cancer antibody, cytotoxic anticancer therapy, or any
other investigational agents within 4 weeks of treatment start

- Known malignancies of the brain or spinal cord or leptomeningeal disease

- Patients requiring pain medication must be on a stable regimen at study entry

- Any condition requiring systemic treatment with corticosteroids (> 10 mg daily
prednisone equivalents) or other immunosuppressive medications within 14 days prior to
first dose of study drug. Inhaled steroids and adrenal replacement steroids > 10 mg
daily prednisone equivalents are allowed in the absence of autoimmune disease

- Uncontrolled pleural effusion, pericardial effusion, or ascites requiring recurrent
drainage procedures (once monthly or more frequently)

- Uncontrolled hypercalcemia (≥ 1.5 mmol/L ionized calcium or Ca ≥ 12 mg/dL or corrected
serum calcium ≥ ULN) or symptomatic hypercalcemia requiring continued use of
bisphosphonate therapy or denosumab

- Diagnosis of another malignancy within 2 years before first dose of study treatment,
except for superficial skin cancers, or localized, low grade tumors deemed cured and
not treated with systemic therapy

- Pregnant and lactating women History of severe allergic, anaphylactic, or other
hypersensitivity reactions to chimeric or humanized antibodies or fusion proteins

- History of HIV infection

- Patients with active or chronic hepatitis B or hepatitis C infection

- Significant cardiovascular disease, such as New York Heart Association cardiac disease
(Class II or greater), myocardial infarction within the previous 6 months, unstable
arrhythmias, unstable angina, or EF < 50%

- Uncontrolled hypertension defined as sustained blood pressure (BP) > 150 mm Hg
systolic or > 100 mm Hg diastolic despite optimal antihypertensive treatment

- Patients with known coronary artery disease, congestive heart failure not meeting the
above criteria must be on a stable medical regimen that is optimized in the opinion of
the treating physician, in consultation with a cardiologist if appropriate

- Major surgery (eg, GI surgery, removal or biopsy of brain metastasis) within 8 weeks
before first dose of study treatment. Complete wound healing from major surgery must
have occurred 1 month before first dose and from minor surgery (eg, simple excision,
biopsy, tooth extraction) at least 10 days before first dose. Subjects with clinically
relevant ongoing complications from prior surgery are not eligible

- History of stroke or transient ischemic attack within 6 months prior to Cycle 1, Day 1

- Significant vascular disease (e.g., aortic aneurysm requiring surgical repair or
recent peripheral arterial thrombosis) within 6 months prior to Cycle 1, Day 1

- Evidence of bleeding diathesis or significant coagulopathy (in the absence of
therapeutic anticoagulation)

- Clinical signs or symptoms of gastrointestinal obstruction or requirement for routine
parenteral hydration, parenteral nutrition, or tube feeding

- Evidence of abdominal free air not explained by paracentesis or recent surgical
procedure

- Patients with a history of abdominal fistula, gastrointestinal perforation, or
intraabdominal abscess within 6 months prior to study enrollment

- Other clinically significant disorders that would preclude safe study participation

- Serious non-healing wound/ulcer/bone fracture

- Uncompensated/symptomatic hypothyroidism

- Moderate to severe hepatic impairment (Child-Pugh B or C)

- Corrected QT interval calculated by the Fridericia formula (QTcF) > 500 ms per
electrocardiogram (ECG) within 28 days before first dose of study treatment Note: If a
single ECG shows a QTcF with an absolute value > 500 ms, two additional ECGs at
intervals of approximately 3 min must be performed within 30 min after the initial
ECG, and the average of these three consecutive results for QTcF will be used to
determine eligibility

- Inability to swallow tablets or capsules

- Previously identified allergy or hypersensitivity to components of the study treatment
formulations

- Patients with a history of non-compliance to medical regimens or who are considered
potentially unreliable or will not be able to complete the entire study

- The subject has prothrombin time (PT)/INR or partial thromboplastin time (PTT) test ≥
1.3 x the laboratory ULN within 14 days of first dose of study treatment

- Concomitant anticoagulation with oral anticoagulants (eg, warfarin, direct thrombin
and Factor Xa inhibitors) or platelet inhibitors (eg, clopidogrel).

Allowed anticoagulants are the following:

- Low-dose aspirin for cardioprotection (per local applicable guidelines) is permitted

- Low-dose low molecular weight heparins (LMWH) are permitted

- Anticoagulation with therapeutic doses of LMWH is allowed in subjects without known
brain metastases who are on a stable dose of LMWH for at least 6 weeks before first
dose of study treatment, and who have had no clinically significant hemorrhagic
complications from the anticoagulation regimen or the tumor

- Clinically significant hematuria, hematemesis, or hemoptysis of > 0.5 teaspoon
(2.5 ml) of red blood, or other history of significant bleeding (eg, pulmonary
hemorrhage) within 12 weeks before first dose

- Cavitating pulmonary lesion(s) or known endotracheal or endobronchial disease
manifestation

- The subject has tumor invading or encasing any major blood vessels

- The subject has evidence of tumor invading the GI tract (esophagus, stomach,
small or large bowel, rectum or anus), or any evidence of endotracheal or
endobronchial tumor within 28 days before the first dose of cabozantinib

- Uncontrolled hypertension (>150 mmHg systolic or > 100 mmHg diastolic despite
optimal antihypertensive treatment)

- Radiation therapy for bone metastasis within 2 weeks, any other radiation therapy
within 4 weeks before first dose of study treatment. Systemic treatment with
radionuclides within 6 weeks before the first dose of study treatment. Subjects
with clinically relevant ongoing complications from prior radiation therapy are
not eligible. Radiation for palliation is allowable on study.