Phase II Study of Abraxane Plus Ipilimumab in Patients With Metastatic Melanoma

Study Drug Administration:

If you are found to be eligible to take part in this study, you will receive ABI-007 by vein
over about 30 minutes on Days 1, 8, and 15 of each 28-day cycle. During the first 3 months
that you receive abraxane, you will also receive ipilimumab. You will receive ipilimumab by
vein over about 90 minutes. You will receive it 4 times, each time about 3 weeks apart.

You will be given standard drugs to help decrease the risk of side effects. You may ask the
study staff for information about how the drugs are given and their risks.

Study Tests:

Every week, blood (about 1 teaspoon) will be drawn for routine tests.

Before each cycle of abraxane:

- Your performance status will be recorded.

- You will have a physical exam, including measurement of your weight and vital signs.

- Blood (about 1 teaspoon) will be drawn for routine tests.

- Blood (about 1 teaspoon) will be drawn for tests of the immune system (first 3 cycles
only).

- You will be asked about any other drugs you may be taking and about any side effects you
may be having.

- If you are able to become pregnant, you will have a blood (about 1 teaspoon) or urine
pregnancy test.

Every 8 weeks (+/- 7 days), you will have a chest x-ray and CT scans or MRI scans performed
to check the status of the disease.

Length of Study:

You may receive ipilimumab for up to 3 months. You may continue taking abraxane for as long
as the doctor thinks it is in your best interest. You will no longer be able to take the
study drugs if the disease gets worse or intolerable side effects occur.

If you stop receiving the study drugs for any reason, you will have an End-of-Treatment
Visit.

End-of-Treatment Visit:

Within 14 days after you stop study treatment, you will come into the clinic for the
End-of-Treatment Visit. At this visit, the following tests will be performed:

- You will have a physical exam, including measurement of your vital signs and weight.

- You will be asked about any other drugs you may be taking and any side effects you may
be having.

- Blood (about 2 tablespoons) will be drawn for routine tests.

- If the study doctor thinks it is in your best interest, you will have a CT scan or MRI
scan to check for side effects.

Every 2 months for 6 months, then every 3 months for up to 2 years, you will also be
contacted by telephone or during a routine clinic visit to see how you are doing. If you are
called, each call should last about 5 minutes.

This is an investigational study. Ipilimumab is FDA approved and commercially available for
the treatment of metastatic melanoma. abraxane is FDA approved and commercially available for
the treatment of metastatic breast cancer. It is investigational to use abraxane, either
alone or in combination with ipilimumab, for the treatment of metastatic melanoma.

Up to 64 patients will take part in this study. All will be enrolled at MD Anderson.

Inclusion Criteria:

1. Patients with histologically documented diagnosis of advanced stage IV or unresectable
stage III mucosal or cutaneous melanoma are eligible.

2. They must have recurrent melanoma with measurable or evaluable sites of disease, 1.0
cm or larger, in order to assess the response to treatment by the immune-related
response criteria (irRC).

3. Patients should not have been previously treated with cytotoxic drugs and
immunotherapeutic agents for unresectable Stage III or Stage IV disease. Prior
Ipilimumab in metastatic setting is not allowed. Prior therapy may include one line of
targeted therapy for metastatic disease ie BRAF or MEK inhibitor. At least 3 weeks
should have passed since the last dose of prior adjuvant interferon therapy and prior
targeted therapies, and all previous therapy related toxicities should have resolved
before starting study treatment. Prior adjuvant interferon is permitted. Prior
cytotoxic therapy in adjuvant or metastatic setting is not allowed. Prior Ipilimumab
in adjuvant setting is not allowed. Prior adjuvant therapy with targeted therapy
including but not limited to B-RAF, MEK inhibitors etc. is allowed. Prior palliative
radiation therapy for metastatic melanoma is permitted provided the patient has
unirradiated metastatic sites for response evaluation and has fully recovered from its
toxicity.

4. Patients between 12 years of age and 70 years of age with an ECOG performance status
of 0 or 1 will be eligible

5. They should have normal blood counts with a white blood cell count of more than or
equal to 3000/mm^3 an absolute neutrophil count of more than or equal to 1500/mm^3 and
a platelet count of more than 100,000/mm^3, Hemoglobin > 9.0 g/dL and have no
impairment of renal function (serum creatinine less than 1.1 mg/dl for females and
less than 1.4 mg/dl for males), hepatic function (serum bilirubin level of less than
1.5 mg/dl, AST and ALT case AST and ALT significant cardiac or pulmonary dysfunction.

6. They should have no significant intercurrent illness such as an active infection
associated with fever lasting more than 24 hours requiring antibiotics, uncontrolled
psychiatric illness, hypercalcemia (calcium greater than 11 mg), or active GI
bleeding. Females of child-bearing potential (non-childbearing is defined as greater
than one year post-menopausal or surgically sterilized) must use acceptable
contraceptive methods( abstinence, intrauterine device, oral contraceptive or double
barrier devices) and must have a negative serum or urine pregnancy test within 72
hours prior to beginning treatment on this trial. Sexually active men must also use
acceptable contraceptive methods for the duration of time on study and signed informed
consent .

Exclusion Criteria:

1. Patients with metastatic uveal melanoma

2. Patients with bone metastases only.

3. Patients with symptomatic brain or spinal cord metastases or requiring steroid therapy
and patients with leptomeningeal disease. Patients with treated and stable CNS
metastasis for 3 months or more, off steroids are eligible for the study. No major
surgery or radiation therapy within 21 days before starting treatment.

4. Patients with significant cardiac illness such as symptomatic coronary artery disease
or previous history of myocardial infarction, impaired left ventricle function
(Ejection Fraction less than 50%) on account of any organic disease such as
hypertension or valvular heart disease or serious cardiac arrhythmia requiring
therapy. Patients with significant history of cardiac disease will be evaluated by the
investigator or his designee.

5. Patients with significant impairment of pulmonary function on account of chronic
bronchitis, emphysema or chronic obstructive pulmonary disease (COPD) which has
resulted in impairment of vital capacity of FEV1 to less than 75% of predicted normal
values.

6. Patients with symptomatic effusions on account of pleural, pericardial or peritoneal
metastases of melanoma.

7. Patients who are unable to return for follow-up visits as required by this study.
Patients with a history of second malignant tumor, other than the common skin cancers
- basal and squamous carcinomas, within the past 3 years and uncertainty about the
histological nature of the metastatic lesions. Cases with other types of malignancies
should be reviewed and decided by the PI of the study.

8. Patients with ≥ grade 2 sensory neuropathy at baseline.

9. Patients who have had major surgery or radiation therapy within 21 days of starting
treatment.