A Study of Pomalidomide (CC-4047) Monotherapy for Children and Young Adults With Recurrent or Progressive Primary Brain Tumors

This is a Phase 2 multi-center, open-label, parallel-group study that will assess the
efficacy, safety and tolerability of pomalidomide in children and young adults aged 1 to < 21
years with recurrent or progressive primary brain tumors after at least one prior standard
therapy.

The study will consist of 4 parallel groups, one for each of the following primary brain
tumor types: high-grade glioma, medulloblastoma, ependymoma and DIPG. A Simon's Optimal
two-stage study design will be applied to each group and enrollment will occur as follows:

- Stage 1: Nine subjects will be enrolled.

- Stage 2: If during Stage 1, ≥ 2 subjects achieves either an objective response (either
CR or PR) within the first 6 cycles of treatment (within first 3 cycles for DIPG), or a
long-term SD, an additional 11 subjects shall be enrolled; otherwise no additional
subjects will be enrolled into that group.

- If a total of 5 or more subjects across all 20 subjects in a given group (Stage 1 and 2)
evaluable for the primary endpoint are observed as having either an objective response
(either CR or PR) within the first 6 cycles of treatment (within first 3 cycles for
DIPG) or a long-term SD, pomalidomide will be considered effective in that disease
indication. Subjects who do not meet the criteria for an objective response or disease
progression by the end of Cycle 6 (end of Cycle 3 for DIPG subjects) will be considered
as having long-term SD.

Response evaluations will be based on MRI results obtained at each site and will be assessed
both locally and by an independent central reviewer. Corticosteroid use and clinical
assessments (ie, neurologic status) will also be considered when determining overall
response.

Tumor assessments will be conducted by standard MRI with and without contrast using three MRI
sequences (T1-weighted pre- and post-contrast, T2-weighted, fluid-attenuated inversion
recovery [FLAIR]). Overall radiographic objective response will be assessed utilizing the
sequence(s) best representative of tumor in the opinion of the neuroradiologist.

Once treatment has been discontinued, subjects will be followed up for up to 5 years from
enrollment of the last subject.

Subjects who withdraw from either stage for reasons other than disease progression prior to
completing Cycle 1 of study treatment will be replaced.

An independent Data Monitoring Committee will monitor the study conduct.

Inclusion Criteria:

1. Subject is 1 to < 21 years of age at the time of signing the Informed Consent
Form/Informed Assent Form (ICF/IAF).

2. Subject (when applicable, parental/legal representative) must understand and
voluntarily sign an ICF/IAF prior to any study-related assessments/procedures being
conducted.

3. Subject has received at least one prior standard therapy (or generally accepted
upfront therapy if no standard exists) and have no known curative therapy.

4. Subject has a diagnosis of high-grade glioma, medulloblastoma, ependymoma or Diffuse
intrinsic pontine glioma (DIPG) that is recurrent or progressive. Subjects with
neurofibromatosis type 1 (NF-1) associated tumors are eligible if the meet all other
eligibility criteria.

5. Subject has histological verification of tumor either at the time of diagnosis or
recurrence. Subjects with DIPG are exempt from histologic verification if they have
typical Magnetic resonance imaging (MRI) findings of DIPG

6. Subject has measurable disease defined as a tumor that is measurable in 2
perpendicular diameters on MRI. For a lesion to be considered measurable, it must be
at least twice the slice thickness on MRI (ie, visible on 2 or more axial slices)

7. To document the degree of tumor at study baseline, the following scan(s) must be
obtained:

• A brain MRI with and without contrast (ie, gadolinium) and a spine MRI with contrast
within 21 days prior to first dose of study treatment. For subjects on steroids,
baseline MRI scans must be performed while on stable or decreasing dose of steroids
for at least 5 days.

8. Subject has Karnofsky (age ≥ 16 years) or Lansky (age < 16 years) performance status
score ≥ 50 at screening

9. Subject has adequate bone marrow function defined as:

- Peripheral Absolute neutrophil count (ANC) ≥ 1000/mm33

- Platelet count ≥ 100,000/mm3 (transfusion independent defined as no platelet
transfusion within 7 days and recovery from nadir)

- Hemoglobin ≥ 8 g/dL (red blood cell [RBC] transfusion is allowed)

10. Subject has adequate renal function defined as:

Adequate real function with Sserum creatinine based on age/gender calculated using the
Schwartz formula as described in protocol, or a 24-hour creatinine clearance or
radioisotope glomerular filtration rate (GFR) (radioisotope or iothalamate) ≥ 70
mL/min/1.73 m2.

11. Subject has adequate liver function defined as:

- Total bilirubin ≤ 1.5 X upper limit of normal (ULN) for current age (≤ 3 X ULN if
increase in bilirubin is attributable to Gilbert's Syndrome)

- Alanine aminotransferase (ALT) (SPGT) is ≤ 3 X ULN for age

- Serum albumin ≥ 3 g/dL

12. Subject has adequate pulmonary function defined as:

- No evidence of dyspnea at rest

- A pulse oximetry ≥ 93%

13. Subject has recovered from clinically significant acute treatment related toxicities
from all prior therapies. Recovery is defined as a toxicity Grade ≤ 2 (common
terminology criteria for adverse events [CTCAE] v. 4.03).

14. Subject has no significant worsening in clinical status for a minimum of 7 days prior
to first dose of study drug.

15. Subject (and when applicable, with parental/legal representative) is willing and able
to adhere to the study visit schedule and other protocol requirements.

16. Females of Childbearing Potential (FCBP) and male subjects who have reached puberty
(and when applicable, with parental/legal representative) must agree to undergo
physician-approved reproductive education and discuss the side effects of the study
therapy on reproduction.

17. Females of childbearing potential must agree and meet the following conditions below:
to

- Medically supervised (ie, performed in a clinic) pregnancy testing, including
those who commit to true abstinence. Two pregnancy tests must be conducted prior
to starting pomalidomide. The first pregnancy test must be performed 10 to 14
days prior to the start of pomalidomide and the second pregnancy test must be
performed within 24 hours prior to starting pomalidomide. Females of childbearing
potential with regular or no menstrual cycles must also agree to have pregnancy
tests weekly for the first 28 days study participation, every 28 days while on
study, at study treatment discontinuation, and at Day 28 following pomalidomide
discontinuation. If menstrual cycles are irregular, the pregnancy testing must
occur weekly for the first 28 days of study participation and then every 14 days
while on study, at study treatment discontinuation visit, and at Days 14 and 28
following pomalidomide discontinuation.

- Female subjects must, as appropriate to age and at the discretion of the study
Investigator, either commit to true abstinence from heterosexual contact and/or
agree to the use of two reliable forms of approved and effective contraceptive
methods simultaneously. The two methods of reliable contraception must include
one highly effective method (ie, oral, injectable, or implantable hormonal
contraceptive; tubal ligation; intra-uterine device; vasectomized partner) and
one additional effective barrier method (ie, male condom, diaphragm, cervical
cap) 28 days prior to starting pomalidomide, throughout the entire duration of
study treatment including dose interruptions and 28 days after discontinuation of
pomalidomide.

- All male and female subjects must follow all requirements defined in the
pomalidomide Pregnancy Prevention Program.

18. Male subjects must, as appropriate to age and the discretion of the study physician:

- Practice true abstinence or agree to use a condom during sexual contact with a
pregnant female or a female of child bearing potential while participating in the
study, during dose interruptions and for at least 28 days following pomalidomide
discontinuation, even if he has undergone a successful vasectomy or practices
complete abstinence.

Exclusion Criteria:

1. Subject has a history of non-central line related thrombosis (arterial or venous),
more than one prior central-line related thrombosis or known coagulopathy.

2. Subject has first degree family member with a known hereditary coagulopathy.

3. Subject is actively on anticoagulation therapy.

4. Subject has had major (per Investigator discretion) surgery, with the exception of
tumor resection, within 21 days from first dose of study drug.

5. Subject has previously received (presence of any of the following will exclude a
subject from enrollment):

- Any prior treatment with pomalidomide. Subjects who have prior treatment with
other immunomodulatory compounds (thalidomide, lenalidomide) ARE eligible if they
meet all other eligibility criteria and did not have allergic reactions or other
"significant toxicity" per Investigator discretion associated with lenalidomide
or thalidomide use.

- Myelosuppressive chemotherapy, immunotherapy, or any investigational agent: ≤ 21
days (≤ 42 days if a nitrosourea) prior to screening.

- Biological (anti-neoplastic) therapy: ≤ 7 days prior to screening.

- Immunomodulatory therapy: ≤ 28 days prior to screening.

- Monoclonal antibody treatment and agents with known prolonged half-lives: < 3
halflives have elapsed or ≤ 28 days prior to screening, whichever is longer.

- Prior radiation:

Cranial irradiation, total body irradiation (TBI), or ≥ 50% radiation of pelvis ≤ 3
months prior to screening.

Focal irradiation: ≤ 3 weeks prior to screening if radiation field involved a
nontarget lesion; ≤ 6 weeks prior to screening if radiation field involved a target
lesion. Note: True disease progression following prior irradiation therapy must be
confirmed by Investigator prior to screening.

• Bone marrow transplant: < 6 months since allogeneic bone marrow transplant prior to
screening. < 3 months since autologous bone marrow/stem cell transplant prior to
screening.

< 3 months since stem cell transplant (SCT) or Rescue without TBI with no evidence of
GVHD prior to screening.

• Radioisotopes: fluorothymidine (18FLT) ≤ 72 hours prior to first dose of study drug

6. Subject has received therapy with a known moderate to potent CYP1A2 inhibitor within
14 days or 5 half-lives of first dose of study treatment (whichever is longer).

7. Subject has received colony-stimulating growth factor(s) within 7 days prior to
screening (or within 14 days if subject received polyethylene glycol formulations).

8. Subject is pregnant, breast-feeding or lactating.

9. Subject has an untreated or uncontrolled infection defined as ongoing signs/symptoms
related to the infection without improvement despite appropriate antibiotics,
antiviral therapy and/or other treatment.

10. Subject has active infectious hepatitis, type A, B, or C, or chronic carriers of
hepatitis C.

11. Subject has any prior history of malignancies, other than high-grade glioma,
medulloblastoma, ependymoma or DIPG (Note: radiation-associated gliomas are excluded
from enrollment)

12. Subject who, in the opinion of the Investigator, has any significant medical
condition, laboratory abnormality, or psychiatric illness that would prevent the
subject from participating in the study.

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

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

15. Subject has symptomatic cardiac disorders (CTCAE v. 4.03 Grade 3 and 4)