Study Evaluating the Effects of Food, Cytochrome P450 Inhibition and Induction on the Pharmacokinetics of CC-122

This study will consist of 4 parts. Each part has two periods. The parts may be conducted in
any order. Subjects may participate in 1 part only.

Each subject will participate in a screening phase, a baseline phase in each study period, a
treatment phase in each study period and a follow-up telephone call. Subjects will be
screened for eligibility. Eligible subjects will return to the study center on Day -1 of
Period 1 and will remain at the study center until the last day of Period 2.

Part 1: On Day 1 of Period 1, eligible subjects will be randomized to 1 of 2 sequences. On
Day 1 of each study period, each subject will receive 1 of 2 treatments according to the
sequence in which he or she is randomized.

In Part 2, subjects will receive a single dose of CC-122 in Period 1 and, following an
appropriate washout, multiple doses of itraconazole plus one dose of itraconazole with CC-122
in Period 2.

In Part 3, subjects will receive a single dose of CC-122 in Period 1 and, following an
appropriate washout, multiple doses of fluvoxamine plus one dose of fluvoxamine with CC-122
in Period 2.

In Part 4, subjects will receive a single dose of CC-122 in Period 1 and, following an
appropriate washout, multiple doses of rifampin plus one dose of rifampin with CC-122 in
Period 2.

Inclusion Criteria:

Subjects must satisfy the following criteria to be enrolled in the study:

1. Subject must understand and voluntarily sign an Informed Consent Form (ICF) prior to
any study-related assessments/procedures being conducted.

2. Subject is ≥ 18 and ≤ 55 years of age at the time of signing the ICF.

3. Subject is willing and able to adhere to the study visit schedule and other protocol
requirements.

4. Subject is in good health as determined by a physical exam at screening.

5. Subject agrees to abide by the requirements and restrictions outlined in the CC-122
Pregnancy Prevention Plan for Subjects in Clinical Trials.

6. Female subjects NOT of childbearing potential must:

a. Have been surgically sterilized (hysterectomy or bilateral oophorectomy; proper
documentation required) at least 6 months before screening, or be postmenopausal
(defined as 24 consecutive months without menses before screening, with a
follicle-stimulating hormone [FSH] level of > 40 IU/L at screening).

7. Male subjects must:

a. Practice true abstinence2 (which must be reviewed on a monthly basis, as
applicable, and source documented) or agree to use a barrier method of birth control
(condoms not made out of natural [animal] membrane [latex condoms are recommended])
during sexual contact with a pregnant female or female of childbearing potential
(FCBP)3 while participating in the study, during dose interruptions, and for at least
90 days after the last dose of Investigational Product (IP), even if he has undergone
a successful vasectomy.

8. Subject has body mass index (BMI) ≥ 18 and ≤ 33 kg/m2 at screening.

9. Subject has clinical laboratory safety test results that are within normal limits or

- considered not clinically significant by the Investigator. Platelet count, absolute
neutrophil count, and absolute lymphocyte count must be above the lower limit of
normal at screening.

10. Subject is afebrile, with supine systolic blood pressure (BP) ≥ 90 and ≤ 140 mmHg,
supine diastolic BP ≥ 50 and ≤ 90 mmHg, and pulse rate ≥ 40 and ≤ 110 bpm at
screening.

11. Subject has a normal or clinically acceptable 12-lead ECG at screening. In addition:

1. If male, subject has a QTcF value ≤ 430 msec at screening.

2. If female, subject has a QTcF value ≤ 450 msec at screening.

Exclusion Criteria:

The presence of any of the following will exclude a subject from enrollment:

1. Subject has any significant medical condition, laboratory abnormality, or psychiatric
illness that would prevent the subject from participating in the study.

2. Subject has any condition including the presence of laboratory abnormalities, which
places the subject at unacceptable risk if he/she were to participate in the study.

3. Subject has any condition that confounds the ability to interpret data from the study.

4. Subject has any hypersensitivity, allergy, or other contraindication to the components
of the CC-122, itraconazole, fluvoxamine, or rifampin formulations used in this study
(see IB and product labels for relevant information).

5. Subject is a female of childbearing potential, pregnant, or breastfeeding.

6. Subject was exposed to an investigational drug (new chemical entity) within 30 days
preceding the first dose administration, or five half-lives of that investigational
drug, if known (whichever is longer).

7. Subject has used any prescribed systemic or topical medication (including but not
limited to analgesics, anesthetics, etc) within 30 days or 5 terminal half-lives
(whichever is longer) prior to the first dose administration.

8. Subject has used any non-prescribed systemic or topical medication (including
vitamin/mineral supplements, and herbal medicines) within 14 days prior to the first
dose administration.

9. Subject has used CYP3A and/or CYP1A2 inducers and/or inhibitors (including St. John's
wort) within 30 days prior to the first dose administration.

10. Subject has any surgical or medical condition possibly affecting drug absorption,
distribution, metabolism and excretion, eg, bariatric procedure. Appendectomy and
cholecystectomy are acceptable.

11. Subject donated blood or plasma within 8 weeks before the first dose administration to
a blood bank or blood donation center.

12. Subject has a history of drug abuse (as defined by the current version of the
Diagnostic and Statistical Manual [DSM]) within 2 years before the first dose
administration, or positive drug screening test reflecting consumption of illicit
drugs.

13. Subject has a history of alcohol abuse (as defined by the current version of the DSM)
within 2 years before the first dose administration, or positive alcohol screen.

14. Subject has a CYP1A2*1 allele or a CYP3A4*22 allele (PARTS 2, 3, AND 4 ONLY).

15. Subject is known to have serum hepatitis or known to be a carrier of hepatitis B
surface antigen (HBsAg) or hepatitis C antibody (HCV Ab), or have a positive result to
the test for human immunodeficiency virus (HIV) antibodies at screening.

16. Subject smokes > 10 cigarettes per day, or the equivalent in other tobacco products
(self-reported).

17. Subject has received immunization with a live or live attenuated vaccine within 2
months prior to administration of the first dose of IP or is planning to receive
immunization with a live or live attenuated vaccine for 2 months after administration
of the last dose of IP.

18. Subject is part of the clinical staff personnel or a family member of the clinical
site staff.