Effect of P-glycoprotein Inhibition on Lenalidomide Pharmacokinetics in Healthy Males

This will be a single-center, open label, 2-part study. Part 1 will be a two-period,
fixed-sequence crossover study with lenalidomide alone in Period 1, followed by lenalidomide
in combination with quinidine in Period 2. Part 2 will be a fixed-sequence, three-period,
crossover study with lenalidomide alone in Period 1, temsirolimus (via direct intravenous
infusion) in Period 2, and lenalidomide in combination with temsirolimus (via direct
intravenous infusion) in Period 3. Diphenhydramine (given via intravenous injection) will be
administered shortly before temsirolimus in order to decrease the chances of an allergic
reaction to temsirolimus. Part 1 and Part 2 will be conducted at the same time. Subjects can
only participate in either Part 1 or Part 2.

Inclusion Criteria:

- Must understand and voluntarily sign a written informed consent form prior to any
study-related procedures being performed.

- Must be able to communicate with the investigator, understand and comply with the
requirements of the study, and agree to adhere to restrictions and examination
schedules.

- Healthy male volunteer of any race between 18 to 65 years of age (inclusive), and in
good health as determined by a physical exam.

- Agree to use barrier contraception (i.e., condoms not made of natural (animal)
membrane [e.g., latex or polyurethane condoms are acceptable]) when engaging in
sexual activity with a female of child-bearing potential while on study drug, and for
at least 90 days after the last dose of study drug.

- Must have a body mass index between 18 and 33 kg/m2 (inclusive).

- Clinical laboratory tests must be within normal limits or acceptable to the principal
investigator.

- Must have confirmation of normal renal function (defined as an estimate glomerular
filtration rate >90 mL/min).

- Must be afebrile, with supine systolic blood pressure: 90 to 140 mmHg, supine
diastolic blood pressure: 60 to 90 mmHg, and pulse rate: 40 to 110 bpm.

- Must have a normal or clinically acceptable 12-lead electrocardiogram, with a QTcF
(Fridericia's correction formula) value ≤ 430 msec.

- Must refrain from sperm donations for the entire duration of the study, and for at
least 90 days after the last dose of study drug.

Exclusion Criteria:

- History of any clinically significant and relevant neurological, gastrointestinal,
renal, hepatic, cardiovascular, psychological, pulmonary, metabolic, endocrine,
hematological, allergic disease, drug allergies, known hypersensitivity to a member
of the class of immunomodulatory drugs (IMiDs®), temosirolimus, sirolimus,
polysorbate 80, diphenhydramine, or to any other component (or excipients) of
Torisel®, or other major disorders.

- Any condition which places the subject at unacceptable risk if he were to participate
in the study, or confounds the ability to interpret data from the study.

- Used any prescribed systemic or topical medication within 30 days of the first dose
administration, unless Sponsor agreement is obtained.

- Used any non-prescribed systemic or topical medication (including vitamin/mineral
supplements, and herbal medicines) within 14 days of the first dose administration,
unless Sponsor agreement is obtained.

- Used any prescribed, or non-prescribed, systemic or topical medication that is a
CYP3A inhibitor or inducer within 30 days of first dose administration. (refer to
(http://medicine.iupui.edu/clinpharm/ddis/p450_Table_Oct_11_2009.pdf)

- Has any surgical or medical conditions (excluding appendectomy) possibly affecting
drug absorption, distribution, metabolism and excretion, e.g., bariatric procedure.

- Donated blood or plasma within 8 weeks before the first dose administration to a
blood bank or blood donation center.

- History of drug abuse (as defined by the current version of the Diagnostic and
Statistical Manual within 2 years before dosing, or positive drug screening test
reflecting consumption of illicit drugs.

- History of alcohol abuse (as defined by the current version of the Diagnostic and
Statistical Manual) within 2 years before dosing, or positive alcohol screen.

- Known to have serum hepatitis or known to be a carrier of the hepatitis B surface
antigen (HBsAg), or hepatitis C antibody (HCVAb), or have a positive result to the
test for HIV antibodies at Screening.

- Exposed to an investigational drug (new chemical entity) within 30 days preceding the
first dose administration, or 5 half-lives of that investigational drug, if known
(whichever is longer).

- For Part 2 only: has total bilirubin ≥ 1.5x upper limit of normal