Study to Determine the Maximum Tolerated Dose for the Combination of Pomalidomide, Bortezomib and Low-Dose Dexamethasone in Subjects With Relapsed or Refractory Multiple Myeloma

A 3 + 3 design will be utilized to determine the MTD for POM + IV BTZ + LD-DEX combination
treatment in a 21-day treatment cycle. DLT will be assessed to determine MTD during the first
treatment cycle. Once the MTD is determined or the maximum planned dose (MPD) is reached
without reaching MTD for POM + IV BTZ + LD-DEX, a cohort of 6 additional subjects will be
treated at this MTD/MPD level to further confirm the safety and assess preliminary efficacy.
An additional cohort of subjects will be enrolled to explore the safety for the combination
of POM + BTZ + LD-DEX when using SQ BTZ. Subject in this cohort will receive POM + BTZ +
LD-DEX at the MTD/MPD level per the MTD determination part of the study, except, the BTZ will
be administered subcutaneously (SQ) instead of intravenously (IV). In, Protocol Amendment #4,
the number of subject enrolled to be enrolled into the exploratory SQ BTZ cohort was
increased from 6 to 12.

Inclusion criteria:

1. Must be ≥ 18 years at the time of signing the informed consent form.

2. Subjects must have documented diagnosis of multiple myeloma and have measurable
disease (serum M-protein ≥ 0.5 g/dL or urine M-protein ≥ 200 mg/24 hours).

3. Subjects must have had at least 1 but no greater than 4 prior anti-myeloma therapies.

4. Subjects must have received at least 2 consecutive cycles of prior treatment with
lenalidomide and must be refractory to their last lenalidomide-containing regimen
(either as a single agent or in combination).

5. Subjects must have received at least 2 consecutive cycles of prior treatment with a
proteasome inhibitor-containing regimen, but must not be refractory to bortezomib
(either as a single agent or in combination).

6. Subjects must have documented progression during or after their last anti-myeloma
therapy.

7. Subjects must have an Eastern Cooperative Oncology Group (ECOG) performance status
score of 0, 1, or 2.

Exclusion criteria:

1. Subjects who are refractory to bortezomib either as single agent or in combination.

2. Subjects with peripheral neuropathy ≥ Grade 2

3. Subjects with non-secretory multiple myeloma

4. Subjects with any of the following laboratory abnormalities:

- Absolute neutrophil count (ANC) < 1,000/µL

- Platelet count < 75,000/µL for subjects in whom < 50% of bone marrow nucleated
cells are plasma cells; or a platelet count < 30,000/ µL for subjects in whom ≥
50% of bone marrow nucleated cells are plasma cells

- Creatinine Clearance < 45 mL/min according to Cockcroft-Gault formula

- Corrected serum calcium > 14 mg/dL (> 3.5 mmol/L)

- Hemoglobin < 8 g/dL (< 4.9 mmol/L; prior RBC transfusion or recombinant human
erythropoietin use is permitted)

- Serum glutamic oxaloacetic transaminase (SGOT)/ aspartate aminotransferase (AST)
or Transaminase, serum glutamic pyruvic (SGPT)/ alanine aminotransferase (ALT) >
3.0 x upper limit of normal (ULN)

- Serum total bilirubin > 1.5 x ULN

5. Subjects with prior history of malignancies, other than MM, unless the subject has
been free of the disease for ≥ 5 years. Except the following: Basal cell carcinoma of
the skin, Squamous cell carcinoma of the skin, Carcinoma in situ of the cervix,
Carcinoma in situ of the breast, Incidental histologic finding of prostate cancer (T1a
or T1b using the TNM [tumor, nodes, metastasis] clinical staging system) or prostate
cancer that is curative.

6. Subjects with previous therapy with Pomalidomide

7. Subjects with hypersensitivity to thalidomide, lenalidomide, bortezomib, boron,
mannitol, or dexamethasone

8. Subjects with ≥ Grade 3 rash during prior thalidomide or lenalidomide therapy

9. Subjects who had any of the following within the last 14 days of initiation of study
treatment: Plasmapheresis, Major surgery (kyphoplasty is not considered major
surgery), Radiation therapy, Any anti-myeloma drug therapy

10. Subjects who have received any investigational agents within 28 days or 5 half-lives
(whichever is longer) of treatment

11. Pregnant or breastfeeding females

12. Men or women of childbearing potential or their sexual partners who are unwilling to
employ adequate contraception.

13. Subjects with known Human immunodeficiency virus (HIV) positivity or active infectious
hepatitis A, B, or C