NOLAN: Naproxen or Loratadine and Neulasta

In this study, the investigational products are naproxen, a non-steroidal antiinflammatory
drug (NSAID), and loratadine, an anti-histamine. Both agents are being investigated as
prophylactic medications to reduce the incidence and/or severity of bone pain in breast
cancer patients receiving adjuvant or neoadjuvant myelosuppressive chemotherapy and
pegfilgrastim prophylaxis.

Pegfilgrastim treatment is used to stimulate bone marrow to produce more neutrophils to help
fight infections in patients undergoing chemotherapy.

Age 18 years or over

- Eastern cooperative oncology group (ECOG) performance status 0-2

- Female with newly diagnosed, not previously treated with chemotherapy, stage I-III
breast cancer

- Medically eligible to safely receive adjuvant or neoadjuvant chemotherapy,
pegfilgrastim, naproxen and loratadine as determined by the investigator

- Creatinine ≤ 1.5 X upper limit of normal (ULN)

- Planning to receive at least 4 cycles of adjuvant or neoadjuvant chemotherapy

- Planning to receive prophylaxis with pegfilgrastim starting in the first cycle and
continuing throughout each chemotherapy cycle of the treatment period

- Subject has provided informed consent

Exclusion Criteria

- History of other malignancy within the past 5 years, with the following exceptions:

- Adequately treated non-melanoma skin cancer or lentigo maligna without evidence
of disease

- Adequately treated cervical carcinoma in situ without evidence of disease

- Planning to receive weekly chemotherapy

- Ongoing chronic pain, or other painful conditions requiring treatment (including
immediate post-operative treatment of surgical or procedural-associated pain) as
determined by the investigator

- Chronic oral steroid use. Premedication related to the administration of chemotherapy,
and use of anti-emetics is allowed, per usual clinical practice

- Chronic use of oral non-steroidal anti-inflammatory drug (NSAIDs) or oral
antihistamines outside of those dictated by the randomization groups outlined in the
protocol, with the following exception:

- Chronic oral aspirin use for cardiovascular-related indications

- Prior chemotherapy treatment for cancer within 5 years of current breast cancer
diagnosis

- Prior use of granulocyte colony stimulating factor (G-CSF)

- History of clinically significant gastrointestinal (GI) bleeding, history of GI ulcers
or active GI bleeding within 6 months prior to randomization

- History of clinically significant bleeding disorders, thromboembolism within 6 months
prior to randomization

- Currently enrolled in, or less than 30 days since ending, another clinical trial which
includes language directing G-CSF (filgrastim, pegfilgrastim, other) or
granulocyte-macrophage colony-stimulating factor (GM-CSF) (sargramostim) use

- Currently enrolled in, or less than 30 days since ending, another interventional
clinical trial which includes a blinded treatment or blinded treatment arm (whether or
not the subject is randomized to the blinded arm)

- Currently enrolled in, or less than 30 days since ending, another interventional
clinical trial which includes the use of any agent not currently considered to be
standard therapy for the adjuvant or neoadjuvant treatment of stage I-III breast
cancer based on National Comprehensive Cancer Network (NCCN) Clinical Practice
Guidelines in Oncology for Breast Cancer

- Currently enrolled in, or less than 30 days since ending, any pain intervention study

- Female subjects who are pregnant or lactating or of reproductive potential not willing
to employ an effective method of birth control during treatment and for 17 days after
discontinuing study treatment

- History or evidence of any other clinically significant disorder, condition or disease
(with the exception of those outlined above) that, in the opinion of the Investigator
or Amgen, if consulted, would pose a risk to subject safety or interfere with the
study evaluation, procedures or completion