Phase 1 Study of Anti-Macrophage Migration Inhibitory Factor (Anti-MIF) Antibody in Solid Tumors

Main Inclusion Criteria:

- Males and females 18 years of age and older at the time of screening

- Anticipated life expectancy > 3 months at the time of screening

- Arm 1 only: Histologically confirmed malignant solid tumor which is refractory to or
has failed standard treatments, or participant is not considered medically suitable to
receive standard of care treatment or refuses standard of care treatment

- Arm 2 only: Histologically or cytologically confirmed diagnosis of metastatic
adenocarcinoma of the colon or rectum which is refractory to or has failed standard
treatments, or participant is not considered medically suitable to receive standard of
care treatment or refuses standard of care treatment

- Measurable or evaluable disease (as defined in the study protocol)

- Eastern Cooperative Oncology Group (ECOG) Performance Status of 0-1

- Adequate hematological function (as defined in the study protocol)

- Adequate renal function (as defined in the study protocol)

- Adequate liver function (as defined in the study protocol)

- Adequate venous access

- Arm 2 only: At least 1 tumor that is amenable to biopsy, as determined by the
investigator, and participant must be willing to undergo a biopsy prior to and at
least once following anti-macrophage migration inhibitory factor (anti-MIF) antibody
treatment

- For women of childbearing potential, the participant must have a negative pregnancy
test at screening and must agree to employ 2 forms of adequate contraceptive measures

- For males, participants must agree to use adequate contraceptive measures including at
least 1 barrier method, and abstain from sperm donation throughout the course of the
study and for at least 90 days after the last administration of investigational
product.

- Participant is willing and able to comply with the requirements of the protocol

Main Exclusion Criteria:

- Known brain tumors or Central nervous system (CNS) metastases

- Myocardial infarction within 6 months of anti-MIF antibody administration, congestive
heart failure (New York Heart Association Class III or Class IV), unstable angina,
unstable cardiac arrhythmia requiring medication, or risk factors for polymorphic
ventricular tachycardia

- Uncontrolled hypertension

- Left ventricular ejection fraction (LVEF) <40%, as determined by screening
echocardiogram (echocardiogram results obtained within 90 days prior to screening are
acceptable)

- QT/QTc interval >450 msec, as determined by screening electrocardiogram (ECG)

- Antitumor therapy (chemotherapy, radiotherapy, antibody therapy, molecular targeted
therapy, retinoid therapy, or hormonal therapy) within 4 weeks prior to administration
of the investigational product (IP) (6 weeks for nitrosoureas and mitomycin C). Any
previous treatment-related toxicities must have recovered to Grade ≤ 1 (graded
according to the National Cancer Institute Common Terminology Criteria for Adverse
Events (NCI CTCAE) v4.03). Prior and concurrent use of hormone deprivation therapies
for hormone-refractory prostate cancer or breast cancer are permitted.

- Major surgery within 4 weeks prior to IP administration

- Active joint inflammation or history of inflammatory arthritis or other immune
disorder involving the joints

- Active infection requiring IV antibiotics within 2 weeks prior to screening

- Known history of hepatitis B virus (HBV), hepatitis C virus (HCV), or active
tuberculosis. Known history of human immunodeficiency virus (HIV) type 1/2 or other
immunodeficiency disease.

- Participant has received a live vaccine within 4 weeks prior to screening

- Known hypersensitivity to any component of recombinant protein production by Chinese
Hamster Ovary (CHO) cells

- Participant has been exposed to an investigational product (IP) or investigational
device in another clinical study within 4 weeks prior to IP administration, or is
scheduled to participate in another clinical study involving an IP or investigational
device during the course of this study

- Participant is nursing or intends to begin nursing during the course of the study

- Any disorder or disease, or clinically significant abnormality on laboratory or other
clinical test(s), that in medical judgment may impede the participant's participation
in the study, pose increased risk to the participant, or confound the results of the
study

- Participant is a family member or employee of the investigator