Pfizer PF-06688992 in Patients With Stage III or Stage IV Melanoma

Inclusion Criteria:

- Histological diagnosis of melanoma confirmed at MSKCC

- Measurable unresectable Stage III or IV Malignant Melanoma and Response Criteria in
Solid Tumors [RECIST], Version 1.1.

- Patients must have progressed on prior approved checkpoint inhibitor therapy, not
tolerated approved checkpoint inhibitor therapy, or have a contraindication to
approved checkpoint inhibitors. Patients with stable disease after approved checkpoint
inhibitor therapy will also be eligible.

- Patients whose melanomas harbor a BRAF V600E or V600K mutation must have progressed on
a RAF inhibitor. Patients who had to discontinue RAF inhibitor therapy because of
toxicity but who did not progress will be eligible unless they responded to therapy.
In that case, they will not be eligible unless they progress.

- Age ≥ 18 years

- ECOG performance status 0-1.

- Adequate Bone Marrow Function as defined by:

°≥1,500/mm^3 or ≥ 1.5 x 10^9/L;

- Platelets ≥ 100,000/mm3 or ≥ 100 x 109/L;

- Hemoglobin ≥ 9 g/dL.

- Adequate Renal Function as defined by:

- Serum creatinine ≤ 1.5 x upper limit of normal (ULN); or

- Estimated creatinine clearance ≥ 60 mL/min as calculated using the method
standard for the institution.

- Adequate Liver Function as defined by:

- Total serum bilirubin ≤ 1.5 x ULN unless the patient has documented Gilbert
syndrome;

- Aspartate and Alanine Aminotransferase (AST & ALT) ≤ 2.5 x ULN; ≤ 5.0 x ULN if
there is liver involvement secondary to tumor;

- Alkaline phosphatase ≤ 2.5 x ULN; (≤ 5 x ULN in case of bone metastasis).

- QTc interval < 470 msec.

- Recovery from all prior surgical or adjuvant treatment-related toxicities, to Baseline
status, or a CTCAE Grade of 0 or 1, except for toxicities not considered a safety
risk, such as alopecia. Post-surgical pain will not be considered a basis for
exclusion.

- Negative serum/urine pregnancy test (for women of childbearing potential).

- Male and female patients of childbearing potential must agree to use a highly
effective method of contraception throughout the study and for at least 28 days after
the last dose of assigned treatment. A patient is of childbearing potential if, in the
opinion of the investigator, he/she is biologically capable of having children and is
sexually active.

- Evidence of a signed and dated informed consent document indicating that the patient
has been informed of all pertinent aspects of the study.

- Willingness and ability to comply with the study scheduled visits, treatment plans,
laboratory tests and other procedures.

Exclusion Criteria:

- Patients with known symptomatic brain metastases requiring steroids.

- Patients with previously diagnosed brain metastases are eligible as long as they do
not require CNS-directed therapy (including corticosteroids). If the patient has had
radiation therapy or surgery, then they should have completed treatment and have
discontinued corticosteroids for at least 2 weeks and must be neurologically stable.

- Patients with uveal melanoma will not be eligible as these tumors show low expression
of GD3.

- Major surgery, radiation therapy or systemic anti-cancer therapy within 2 weeks of
starting study treatment.

- Presence of ≥ Grade 2 peripheral neuropathy.

- Significant prior infusion reaction to monoclonal antibodies that required treatment
with systemic steroids.

- Active and clinically significant bacterial, fungal or viral infection.

- Known infections with hepatitis B (HBV) or hepatitis C (HCV),

- Known human immunodeficiency virus (HIV) or acquired immunodeficiency syndrome
(AIDS)-related illness not controlled (with undetectable viral load) on HAART
therapy. Patients on HAART with undetectable viral loads may be eligible per PI
judgment.

- Pregnant or breastfeeding; males and females of childbearing potential who are
unwilling or unable to use a highly effective method of contraception as outlined in
this protocol for the duration of the study and for at least 28 days after last dose
of investigational product.

- Patients currently receiving active treatment for melanoma.

- Any of the following in the previous 6 months: myocardial infarction, severe/unstable
angina, coronary/peripheral artery bypass graft, symptomatic congestive heart failure,
cerebrovascular accident, transient ischemic attack.

- Any ongoing cardiac dysrhythmias of NCI CTCAE Grade >2, NCI CTCAE Grade 4 atrial
fibrillation, or QTcF interval >470 msec, except for documented Right Bundle Branch
Block, at screening.

- Chronic Bronchitis or Emphysema requiring oxygen therapy within the last 6 months.

- Other severe acute or chronic medical or psychiatric condition, including recent
(within the past year) or active suicidal ideation or behavior, or laboratory
abnormality or uncontrolled hypertension that may increase the risk associated with
study participation or investigational product administration or may interfere with
the interpretation of study results and, in the judgment of the investigator, would
make the patient inappropriate for entry into this study.