A Safety Trial of Nivolumab in Patients With Advanced or Metastatic Non-Small Cell Lung Cancer Who Have Progressed During or After Receiving At Least One Prior Chemotherapy Regimen

For more information regarding BMS clinical trial participation, please visit
www.BMSStudyConnect.com

Inclusion Criteria:

1. Target Population

- Subjects with histologically-or cytologically-documented NSCLC [squamous (SQ) or
nonsquamous (NSQ)] who present with Stage IIIB/Stage IV disease (according to version
7 of the International Association for the Study of Lung Cancer Staging Manual in
Thoracic Oncology), or with recurrent or progressive disease following multimodal
therapy (radiation therapy, surgical resection or definitive chemoradiotherapy for
locally advanced disease)

- Subjects must have experienced disease progression or recurrence during or after at
least one systemic therapy for advanced or metastatic disease

- Each subsequent line of therapy must be preceded by disease progression. A switch of
an agent within a regimen in order to manage toxicity does not define the start of a
new line of therapy

- Maintenance therapy following platinum doublet-based chemotherapy is not considered as
a separate regimen of therapy

- Subjects who received platinum-containing adjuvant, neoadjuvant or definitive
chemoradiation therapy given for locally advanced disease, and developed recurrent
(local or metastatic) disease within 6 months of completing therapy are eligible

- Subjects with recurrent disease >6 months after platinum-containing adjuvant,
neoadjuvant or definitive chemoradiation therapy given for locally advanced disease,
who also subsequently progressed during or after a platinum doublet-based regimen
given to treat the recurrence are eligible

- Subjects with non-squamous histology must be tested for Epithelial Growth Factor
Receptor (EGFR) mutations (including, but not limited to, deletions in exon 19 and
exon 21 [L858R] substitution) and Anaplastic Lymphoma Kinase (ALK) rearrangement if
tests have not been previously performed. Subjects with progressive disease during or
after EGFR or ALK tyrosine kinase inhibitor (TKI) regimens are eligible. Subjects are
eligible if genetic test results are indeterminate or if no tumor tissue is available
or accessible for testing as long as they have received one prior systemic therapy

- Experimental therapies when given as separate regimen are considered as separate line
of therapy

- Subjects must have measurable disease by CT or MRI per RECIST 1.1 criteria
(radiographic tumor assessment performed within 28 days of first dose of study drug)
or clinically apparent disease that the investigator can follow for response per
RECIST 1.1

- Eastern Cooperative Oncology Arm (ECOG) performance status (PS)

- PS 0 to 1

- PS 2

Exclusion Criteria:

1. Target Disease Exceptions

- Subjects with active central nervous system (CNS) metastases are excluded

- Subjects with carcinomatous meningitis

2. Medical History and Concurrent Diseases

- Subjects with a history of interstitial lung disease

- Subjects with active, known or suspected autoimmune disease

- Subject whom participated in either arm of the following clinical trials
CA209-017, CA209-057, CA209-026, and CA184-104 or received prior treatment with
anti-programmed death 1 (PD-1) or anti-programmed death-ligand 1 (PDL1)
experimental agents

3. Prohibited Treatments and/or Restricted Therapies

- Ongoing or planned administration of anti-cancer therapies other than those
specified in this study

- Use of corticosteroids or other immunosuppressive medications