Phase 1b Study Evaluating ACY-1215 (Ricolinostat) in Combination With Pomalidomide and Dexamethasone in Relapsed or Relapsed-and-Refractory Multiple Myeloma

To determine the maximum tolerated dose (MTD), if present, and to identify a recommended dose
and schedule of ricolinostat administered in an alternative liquid formulation (ALF)
(10mg/mL) in combination with pomalidomide and low-dose dexamethasone in patients with
relapsed or relapsed-and-refractory multiple myeloma.

To evaluate the safety and any anti-tumor activity of ricolinostat administered in
combination with pomalidomide and dexamethasone as treatment for patients with relapsed or
relapsed-and-refractory multiple myeloma, including duration of response.

To assess the Pharmacokinetics and Pharmacodynamics of all three medications administered in
combination, and to assess the Pharmacokinetics of ricolinostat and pomalidomide
specifically. An evaluation of the relationship between response and biomarkers relating to
interacellular acetylation may also be completed.

Key Inclusion Criteria Includes:

Patients meeting all of the following criteria may be enrolled in the study:

1. Must be able to understand and voluntarily sign an ICF.

2. Must be registered into the mandatory POMALYST Risk Evaluation and Mitigation Strategy
(REMS)™ program, and be willing and able to comply with the requirements of the
POMALYST REMS™ program (Appendix 9.3).

3. Must be ≥ 18 years of age at the time of signing the ICF.

4. Must be able to adhere to the study visit schedule and other protocol requirements.

5. Must have a documented diagnosis of MM and have relapsed or relapsed and refractory
disease. Patients must have received at least 2 lines of prior therapies. Patients
must have relapsed after having achieved at least stable disease for at least 1 cycle
of treatment to at least 1 prior regimen and then developed PD. Relapsed and
relapsed-and-refractory patients must have documented evidence of PD during or within
60 days (measured from the end of the last cycle) of completing treatment with the
last antimyeloma drug regimen used just prior to study entry.

6. Patients must have undergone prior treatment with at least 2 cycles of lenalidomide
and at least 2 cycles of a proteasome inhibitor (either in a separate regimen or
within the same regimen.

7. Must not be a candidate for autologous stem cell transplant (ASCT), have declined the
option of ASCT, or have relapsed after prior ASCT.

8. Must have measurable levels of myeloma paraprotein in serum (≥ 0.5 g/dL) or urine (≥
0.2 g/24 hours). Patients who do not have myeloma paraprotein must have serum free
light chain (SFLC) concentration of ≥ 10 mg/dL, provided SFLC ratio is abnormal.
Nonsecretory myeloma is excluded.

9. Must have Eastern Cooperative Oncology Group performance status score of 0, 1, or 2.

10. Females of childbearing potential must have a negative serum or urine pregnancy test
as described in Appendix 9.3 for the POMALYST REMS™ program. Females of childbearing
potential and males must either commit to continued abstinence from heterosexual
intercourse or must abide by birth control requirements as described in Appendix 9.3
for the POMALYST REMS™ program.

11. Must agree to refrain from donating blood while on study drug and for 28 days after
discontinuation from this study.

12. Must agree not to share study medication with another person.

13. Must be able to take ASA (81 or 325 mg) daily as prophylactic anticoagulation.
Patients intolerant to ASA may use low molecular weight heparin. Lovenox is
recommended. Coumadin will be allowed provided the patient is fully anticoagulated,
with an international normalized ratio of 2 to 3.

Key Exclusion Criteria Includes:

Patients meeting any of the following criteria will be excluded from enrollment in the
study:

1. Any serious medical condition, laboratory abnormality, or psychiatric illness that
would prevent the patient from signing the ICF or from following the study
requirements.

2. Pregnant or lactating females.

3. Prior therapy with histone deacetylase inhibitor or pomalidomide.

4. Any of the following laboratory abnormalities:

- ANC < 1,000/µL

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

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

- Creatinine clearance < 45 mL/min according to Cockcroft-Gault formula. If
creatinine clearance calculated from the 24 hour urine sample is ≥ 45 mL/min,
patient will qualify for the trial.

- Serum glutamic oxaloacetic transaminase/aspartate aminotransferase, or serum
glutamic pyruvic transaminase/alanine aminotransferase > 3.0 × ULN

- Serum total bilirubin > 2.0 mg/dL

5. Prior history of malignancies, other than MM, unless the patient has been free of the
disease for ≥ 3 years. Exceptions include the following:

- Basal or squamous cell carcinoma of the skin

- Ductal carcinoma in situ; or cervical intraepithelial neoplasia

- Carcinoma of the prostate with a current prostate-specific antigen below the
upper limit of normal

6. Corrected QT interval (QTc) using Fridericia's formula value > 480 msec at Screening;
family or personal history of long QTc syndrome or ventricular arrhythmias including
ventricular bigeminy at Screening; previous history of drug-induced QTc prolongation
or the need for treatment with medications known or suspected of producing prolonged
QTc intervals on electrocardiogram.

7. Known human immunodeficiency virus, hepatitis B virus, and known or suspected active
hepatitis C virus infection.

8. Hypersensitivity to thalidomide, lenalidomide, pomalidomide, or dexamethasone (such as
Steven Johnson Syndrome). Hypersensitivity, such as rash, that can be medically
managed is allowable.

9. Peripheral neuropathy ≥ Grade 2 despite supportive therapy.

10. Radiotherapy or systemic therapy (standard or an investigational or biologic
anticancer agent) within 14 days of initiation of study drug treatment.

11. Current enrollment in another clinical trial involving treatment and/or receiving an
investigational agent for any reason.

12. Inability or unwillingness to comply with birth control requirements or any of the
POMALYST REMS™ requirements per Appendix 9.3.