Alisertib and Gemcitabine Hydrochloride in Treating Patients With Solid Tumors or Pancreatic Cancer

PRIMARY OBJECTIVES:

I. To investigate the feasibility and safety of MLN8237 (alisertib) when given in combination
with gemcitabine (gemcitabine hydrochloride) to patients with advanced solid tumors.

SECONDARY OBJECTIVES:

I. To determine the maximum tolerated dose (MTD) of MLN8237 when given in combination with
gemcitabine to patients with advanced solid tumors and to recommend a phase II dose for the
combination.

II. To obtain preliminary evidence of efficacy as judged by response rate and
progression-free survival for this combination.

III. To investigate the pharmacokinetics of MLN8237 given in combination with gemcitabine in
an expanded cohort of patients with pancreatic cancer.

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

Patients receive gemcitabine hydrochloride intravenously (IV) over 30 minutes on days 1, 8,
and 15 and alisertib orally (PO) twice daily (BID) on days 1-3, 8-10, and 15-17. Courses
repeat every 28 days in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up periodically.

Inclusion Criteria:

- Eligibility for dose escalation cohort: histologically or cytologically confirmed
metastatic or unresectable solid tumor for which standard curative or palliative
measures do not exist or are no longer effective

- Eligibility for the expansion cohort: histologically or cytologically confirmed
metastatic or unresectable pancreatic adenocarcinoma for which curative treatment does
not exist

- Zubrod (Eastern Cooperative Oncology Group [ECOG]) performance status 0 - 2

- Measurable or non-measurable disease. x-rays and/or scans for disease assessment of
measurable disease must have been completed within 28 days prior to registration;
non-measurable disease must also be assessed within 28 days prior to registration;
(expansion - patients must have measurable disease)

- Absolute neutrophil count (ANC) >= 1,500/mm^3

- Platelet count >= 100,000/mm^3

- Total bilirubin within institutional normal limits

- Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) =< 2.5 times
institutional upper limit of normal or =< 5 times institutional upper limit of normal
in the presence of liver metastases

- Creatinine =< 1.5 times institutional upper limit of normal OR

- Creatinine Clearance >= 60ml/min/1.73m^2 measured by 24-hour urine collection

- Any number of prior chemotherapy regimens; up to two prior chemotherapy regimen in the
palliative setting will be allowed in the expansion cohort. Prior gemcitabine-based
regimes in the palliative setting are permitted if no evidence of progression on
therapy or at least 6 months after discontinuation of gemcitabine based treatment.
Prior gemcitabine in the adjuvant setting is permitted if last treatment was greater
than 6 months prior to registration

- Any prior chemotherapy, immunotherapy or targeted therapy must have been completed at
least 2 weeks prior to start of this protocol and all side effects (except alopecia,
lymphopenia and hyperglycemia) resolved to grade 1 or less; any prior radiation must
have been completed at least 2 weeks prior to start of therapy

- Pregnant or nursing women are ineligible; women of child-bearing potential and men
must agree to use adequate contraception (hormonal or barrier method of birth control;
abstinence) prior to study entry and for the duration of study participation

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

- Ability to swallow and retain oral medications

- Voluntary written informed consent before performance of any study-related procedure
not part of normal medical care, with the understanding that consent may be withdrawn
by the subject at any time without prejudice to future medical care

- Female subject is either post-menopausal or surgically sterilized or willing to use an
acceptable method of birth control (ie, a hormonal contraceptive, intra-uterine
device, diaphragm with spermicide, condom with spermicide, or abstinence) for the
duration of the study

- Male subject agrees to use an acceptable method for contraception during the entire
study treatment period through 4 months after the last dose of MLN8237; male patients,
even if surgically sterilized (ie, status postvasectomy) must agree to practice
effective barrier contraception during the entire study treatment period and through
four months after the last dose of study drug, or completely abstain from heterosexual
intercourse

Exclusion Criteria:

- Prior treatment with Aurora A-targeted agents, including MLN8237

- History of Gilbert's syndrome

- Cardiac disease: congestive heart failure > class II New York Heart Association
(NYHA); patients must not have unstable angina (anginal symptoms at rest) or new onset
angina (began within the last 3 months) or myocardial infarction within the past 6
months

- Symptomatic or uncontrolled brain metastasis; patients with neurological symptoms must
undergo a computed tomography (CT) scan/magnetic resonance imaging (MRI) of the brain
to exclude brain metastasis; previously treated brain metastases will be allowed as
long as the patient is neurologically stable and is off steroids and anticonvulsants

- Prior radiation to greater than 25% of the bone marrow or whole pelvis radiation

- Patients requiring full therapeutic anticoagulation with warfarin are ineligible
because therapy on this trial may result in frequent and recurrent thrombocytopenia;
full therapeutic anticoagulation with heparin, low molecular weight heparin, or direct
factor Xa inhibitor is permitted

- Patients with a diagnosis of active human immunodeficiency virus (HIV) infection, on
anti-retroviral therapy, or with a cluster of differentiation (CD) 4 count less than
200 are ineligible; testing is not required in the absence of clinical findings or
suspicion

- Patients with a diagnosis of chronic hepatitis B are ineligible

- Active clinically serious infection > Common Terminology Criteria for Adverse Events
(CTCAE) grade 2 or systemic infection requiring IV antibiotic therapy within 14 days
preceding the first dose of study drug

- Serious non-healing wound, ulcer, or bone fracture

- Major surgery, open biopsy or significant traumatic injury within 4 weeks of first
dose of study drug

- Known or suspected allergy to gemcitabine or MLN8237, or any agent given in the course
of this trial

- Any clinically significant medical or psychiatric condition that would interfere with
protocol treatment

- Prior allogeneic bone marrow or organ transplantation

- Known history of uncontrolled sleep apnea syndrome and other conditions that could
result in excessive daytime sleepiness, such as severe chronic obstructive pulmonary
disease; requirement for supplemental oxygen

- Requirement for constant administration of proton pump inhibitor or H2 antagonist;
intermittent uses of antacids or H2 antagonists are allowed

- Myocardial infarction within 6 months prior to enrollment or has New York Heart
Association (NYHA) class III or IV heart failure, uncontrolled angina, severe
uncontrolled ventricular arrhythmias, or electrocardiographic evidence of acute
ischemia or active conduction system abnormalities; prior to study entry, any
electrocardiogram (ECG) abnormality at screening has to be documented by the
investigator as not medically relevant

- Female subject is pregnant or breast-feeding; confirmation that the subject is not
pregnant must be established by a negative serum beta-human chorionic gonadotropin
(B-hCG) pregnancy test result obtained during screening; pregnancy testing is not
required for post-menopausal or surgically sterilized women

- Patient has received other investigational drugs with 14 days before enrollment

- Other severe acute or chronic medical or psychiatric condition, including uncontrolled
diabetes, malabsorption, resection of the pancreas or upper small bowel, requirement
for pancreatic enzymes, any condition that would modify small bowel absorption of oral
medications, or laboratory abnormality that may increase the risk associated with
study participation or investigational product administration or may interfere with
the interpretation of study results and, in the judgment of the investigator, would
make the patient inappropriate for enrollment in this study

- Treatment with clinically significant enzyme inducers, such as the enzyme-inducing
antiepileptic drugs phenytoin, carbamazepine or phenobarbital, or rifampin, rifabutin,
rifapentine or St. John's wort within 14 days prior to the first dose of MLN8237 and
during the study