Inclusion Criteria:

1. Has or is willing to give consent to the Treating Physician in accordance with the
local regulatory requirements.

2. Has the following diagnosis: Completely resected (R0) histologically confirmed
high-risk (stage III) cutaneous melanoma with confirmed BRAF V600E/K activating
mutation.

Patients presenting with initial resectable lymph node recurrence after a diagnosis
of Stage I or II melanoma are eligible. Patients with an unknown primary melanoma
are not eligible.

3. All clinical trials that the patient might qualify for have been ruled out.

4. Is receiving care at a clinical site with a Treating Physician who has experience
with administering investigational agents for patients with this condition, or the
patient is willing and/or able to travel to a site and receive treatment under the
guidance of physician with this experience.

5. Is able to retain oral medication and swallow tablets/capsules (appropriate
exceptions allowed for patients who are unable to swallow tablets/capsules - this is
subject to availability of alternative (liquid) oral formulations).

6. Is not eligible for participation in any of the IMP's ongoing clinical trials or has
recently completed a clinical trial that has been terminated and, after considering
other options (e.g., trial extensions, amendments, etc.), the clinical team has
determined that treatment is necessary and there are no other feasible alternatives
for the patient.

7. Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 to 3 (or
equivalent) and is in stable clinical condition. NOTE: patient in rapidly
deteriorating clinical condition prior to start of therapy should not be considered
for this program.

8. Does not require treatment with prohibited concomitant medications (please refer to
the IB or approved label/SmPC).

9. Women of childbearing potential must have had a negative serum β-human chorionic
gonadotropin (HCG) pregnancy test within 7 days prior to starting dabrafenib and
trametinib treatment. Subjects with a positive pregnancy test result must be
excluded from the program. Subjects with a negative pregnancy test result must agree
to use an effective contraception method as described below throughout the treatment
period and for a total of 4 months following the last dose of treatment.

Contraceptive Methods for Females of Childbearing Potential:

- An intrauterine device with a documented failure rate of less than 1% per year

- Vasectomized partner who is sterile prior to the female patient's entry into the
Compassionate Use program, and this male is the sole sexual partner for that female.

- Complete abstinence from sexual intercourse for 14 days prior to first dose of
treatment, through the dosing period, and for at least 4 months after the last dose
of treatment. Abstinence is only acceptable when in line with the preferred and
usual lifestyle of the subject. Periodic abstinence (e.g. calendar, ovulation,
symptothermal, post-ovulation methods, etc.) and withdrawal are not acceptable
methods of contraception.

- Double-barrier contraception: condom and occlusive cap (diaphragm or cervical/vault
caps) with vaginal spermicidal agent (foam/gel/cream/suppository).

Note: Hormonal-based methods (e.g., oral contraceptives) are not permitted as
contraception due to potential drug-drug interactions with dabrafenib.

Females Not of Childbearing Potential Non-childbearing potential (i.e., physiologically
incapable of becoming pregnant) is defined as any female who has had a documented
hysterectomy, bilateral oophorectomy (ovariectomy), bilateral tubal ligation or tubal
occlusion, or is post-menopausal.

A practical definition accepts menopause after 1 year without menses with an appropriate
clinical profile; e.g., age appropriate, >45 years in the absence of hormone replacement
therapy (HRT). In questionable cases, the patient must have a follicle stimulating
hormone (FSH) value >40 mIU/mL and an estradiol value <40 pg/mL (<140 pmol/L).

Female patients determined not to be post-menopausal must use adequate contraception, as
defined immediately above for females of childbearing potential.

Female subjects who are lactating must discontinue nursing prior to the first dose of
program treatment and must refrain from nursing throughout the treatment period and for 4
months following the last dose of program treatment.

If a subject becomes pregnant during the treatment period of the program, the treatments
should be stopped immediately.

Written patient informed consent must be obtained by the Treating Physician prior to
start of treatment in accordance with the applicable local regulatory requirements.

Exclusion Criteria:

Patients eligible for this Treatment Plan must not meet any of the following criteria:

History of hypersensitivity to any drugs or metabolites of similar chemical classes as
the product.

1. Uveal or mucosal melanoma.

2. Evidence of metastatic disease.

3. Female who is pregnant or nursing (patient must discontinue nursing in order to
enroll in the program).

NOTE: Safety and efficacy in pregnant or nursing women has not been investigated.
Inclusion of pregnant or nursing woman may be considered in individually upon review
by the Novartis Country Pharma Organization Medical Advisor/Director.

4. Patients who have any lab abnormalities or AE/SAEs greater than Grade 3 (CTCAE v5.0)

5. Concurrent treatment with other systemic anti-cancer therapies is not allowed, with
the exception of surgery (other exceptions might be allowed and are subject to
individual evaluation). Patients who are currently being treated with another
systemic anti-cancer therapy (e.g., chemotherapy, immune, biologic, or targeted
therapy) must discontinue use prior to initiation of treatment with trametinib and
dabrafenib. NOTE: Radiation skin injury has been reported with concurrent use of
dabrafenib and radiation.

6. Presence of any malignancy with confirmed activating RAS mutation. NOTE: Prospective
RAS testing is not required. However, if the results of previous RAS testing are
known, they must be used in assessing eligibility.

7. Has a known immediate or delayed hypersensitivity reaction or idiosyncrasy to drugs
chemically related to trametinib or dabrafenib, or excipients or to dimethyl
sulfoxide (DMSO).

8. Any medical conditions or physical examination or clinical laboratory findings
which, would put the patient at high risk for an adverse outcome.

9. Current evidence / risk of retinal vein occlusion (RVO) or central serous
retinopathy.

10. Current evidence of cardiovascular risk including any of the following:

- LVEF

- A QT interval corrected for heart rate using the Bazett's formula ≥ 480 msec

- A clinically significant uncontrolled arrhythmias

- Acute coronary syndrome (including myocardial infarction and unstable angina)

- Congestive heart failure ≥ Class II as defined by New York Heart Association

11. Not able to understand and to comply with treatment instructions and requirements.