Study of Dabrafenib, Trametinib and Metformin for Melanoma Patients

The study will be a single-arm, single center, uncontrolled phase I/II trial to estimate the
safety of the combined treatments and then estimate the efficacy in terms of objective
response rate in patients with stage IIIC and Stage IV melanoma treated with
dabrafenib/trametinib and metformin.

Inclusion Criteria:

- Male or female patients > 18 years of age

- Patients with histologically confirmed BRAFV600E melanoma (Stage IIIC or

- Stage IV, American Joint Commission on Cancer)

- Eastern Cooperative Oncology Group Performance Status of 0 to 2

- Life expectancy > 3 months

- At least 1 site of radiographically measurable disease by RECIST 1.1

- Adequate hematologic, renal, and liver function as defined by laboratory values
performed within 42 days prior to initiation of dosing:

- Absolute neutrophil count > 1.0 x 10⁹/L

- Platelet count > 50 x 10⁹/L

- Hemoglobin > 8 g/dL

- Serum creatinine < 2 x upper limit of normal

- Total serum bilirubin < 3 x ULN

- Serum aspartate transaminase or serum alanine transaminase < 3 x ULN, and < 4 x ULN
if liver metastases are present

- Fertile males should use an effective method of contraception during treatment and
for at least 3 months after completion of treatment, as directed by their physician

- Pre-menopausal females and females < 2 years after the onset of menopause should have
a negative pregnancy test at Screening. Pre-menopausal females must agree to use an
acceptable method of birth control from the time of the negative pregnancy test up to
90 days after the last dose of the study drug

- Females of non-childbearing potential may be included if they are either surgically
sterile or have been postmenopausal for > 1 year

- Before study entry, written informed consent must be obtained from the patient prior
to performing any study related procedures

Exclusion Criteria:

- Prior treatment with Vemurafenib or Dabrafenib

- Known hypersensitivity to Metformin or any of its components

- Received radiotherapy for non CNS disease within the 2 weeks prior to commencing
study treatment or have not recovered from side effects of all radiation related
toxicities to Grade < 1, except for alopecia

- Pregnant, breast feeding, or refusing double barrier contraception, oral
contraceptives, or avoidance of pregnancy measures

- Have any other uncontrolled infection or medical condition that could interfere with
the conduct of the study