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BRAFTOVI (encorafenib 50 mg) Dailymed

  1. Human Prescription
  2. BRAF Serine/Threonine Kinase Inhibitors
  3. Array BioPharma Inc.

Generic: encorafenib is used for the treatment of Melanoma

BRAFTOVI capsule - (encorafenib 50 mg) image

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Recent Major Changes Section



Indications and Usage (1.3, 1.4)
10/2023

Dosage and Administration (2.1, 2.2, 2.5)
10/2023

Warnings and Precautions (5.1, 5.3, 5.4, 5.5, 5.6, 5.7, 5.8)
10/2023

1 Indications And Usage



BRAFTOVI is a kinase inhibitor indicated:
  • •in combination with binimetinib, for the treatment of patients with unresectable or metastatic melanoma with a BRAF V600E or V600K mutation, as detected by an FDA-approved test. (1.1, 2.1)
  • •in combination with cetuximab, for the treatment of adult patients with metastatic colorectal cancer (CRC) with a BRAF V600E mutation, as detected by an FDA-approved test, after prior therapy. (1.2, 2.1)
  • •in combination with binimetinib, for the treatment of adult patients with metastatic non-small cell lung cancer (NSCLC) with a BRAF V600E mutation, as detected by an FDA-approved test. (1.3, 2.1)

Limitations of Use

BRAFTOVI is not indicated for treatment of patients with wild-type BRAF melanoma, wild-type BRAF CRC, or wild-type BRAF NSCLC. (1.4, 5.2)

1.1 BRAF V600E or V600K Mutation-Positive Unresectable or Metastatic Melanoma


BRAFTOVI is indicated, in combination with binimetinib, for the treatment of patients with unresectable or metastatic melanoma with a BRAF V600E or V600K mutation, as detected by an FDA-approved test [see Dosage and Administration (2.1)].

1.2 BRAF V600E Mutation-Positive Metastatic Colorectal Cancer (CRC)


BRAFTOVI is indicated, in combination with cetuximab, for the treatment of adult patients with metastatic colorectal cancer (CRC) with a BRAF V600E mutation, as detected by an FDA-approved test, after prior therapy [see Dosage and Administration (2.1)].

1.3 BRAF V600E Mutation-Positive Metastatic Non-Small Cell Lung Cancer (NSCLC)


BRAFTOVI is indicated, in combination with binimetinib, for the treatment of adult patients with metastatic non-small cell lung cancer (NSCLC) with a BRAF V600E mutation, as detected by an FDA-approved test [see Dosage and Administration (2.1)].

1.4 Limitations of Use


BRAFTOVI is not indicated for treatment of patients with wild-type BRAF melanoma, wild-type BRAF CRC, or wild-type BRAF NSCLC [see Warnings and Precautions (5.2)] .

2 Dosage And Administration


  • • Melanoma
    • oConfirm the presence of BRAF V600E or V600K mutation in tumor specimens prior to the initiation of BRAFTOVI. (2.1)
    • oThe recommended dose is 450 mg orally once daily in combination with binimetinib. (2.2)
  • • CRC
    • oConfirm the presence of BRAF V600E mutation in tumor specimens prior to the initiation of BRAFTOVI. (2.1)
    • oThe recommended dose is 300 mg orally once daily in combination with cetuximab. (2.3)
  • • NSCLC
    • oConfirm the presence of BRAF V600E mutation in tumor or plasma specimens prior to initiating BRAFTOVI. (2.1)
    • oThe recommended dose is 450 mg orally once daily in combination with binimetinib. (2.2)
  • •Take BRAFTOVI with or without food. (2.4)

2.1 Patient Selection


BRAF V600E or V600K Mutation-Positive Unresectable or Metastatic Melanoma

Confirm the presence of a BRAF V600E or V600K mutation in tumor specimens prior to initiating BRAFTOVI [see Warnings and Precautions (5.2), Clinical Studies (14.1)]. Information on FDA-approved tests for the detection of BRAF V600E and V600K mutations in melanoma is available at: http://www.fda.gov/CompanionDiagnostics.


BRAF V600E Mutation-Positive Metastatic Colorectal Cancer (CRC)

Confirm the presence of a BRAF V600E mutation in tumor specimens prior to initiating BRAFTOVI [see Warnings and Precautions (5.2), Clinical Studies (14.2) ]. Information on FDA-approved tests for the detection of BRAF V600E mutations in CRC is available at: http://www.fda.gov/CompanionDiagnostics.

BRAF V600E Mutation-Positive Metastatic Non-Small Cell Lung Cancer (NSCLC)

Confirm the presence of a BRAF V600E mutation in tumor or plasma specimens prior to initiating BRAFTOVI [see Warnings and Precautions (5.2), Clinical Studies (14.3)]. If no mutation is detected in a plasma specimen, test tumor tissue. Information on FDA-approved tests for the detection of BRAF V600E mutations in NSCLC is available at: http://www.fda.gov/CompanionDiagnostics.


The recommended dosage of BRAFTOVI is 450 mg (six 75 mg capsules) orally once daily in combination with binimetinib until disease progression or unacceptable toxicity. Refer to the binimetinib prescribing information for recommended binimetinib dosing information.

2.3 Recommended Dosage for BRAF V600E Mutation-Positive Metastatic Colorectal Cancer (CRC)


The recommended dosage of BRAFTOVI is 300 mg (four 75 mg capsules) orally once daily in combination with cetuximab until disease progression or unacceptable toxicity. Refer to the cetuximab prescribing information for recommended cetuximab dosing information.

2.4 Administration


BRAFTOVI may be taken with or without food [see Clinical Pharmacology (12.3)]. Do not take a missed dose of BRAFTOVI within 12 hours of the next dose of BRAFTOVI.

Do not take an additional dose if vomiting occurs after BRAFTOVI administration but continue with the next scheduled dose.

2.5 Dosage Modifications for Adverse Reactions



BRAF V600E or V600K Mutation-Positive Unresectable or Metastatic Melanoma or BRAF V600E Mutation-Positive Metastatic NSCLC

If binimetinib is withheld, reduce BRAFTOVI to a maximum dose of 300 mg (four 75 mg capsules) once daily until binimetinib is resumed [see Warnings and Precautions (5.9) ].

Dose reductions for adverse reactions associated with BRAFTOVI are presented in Table 1.

Table 1: Recommended Dose Reductions for BRAFTOVI for Adverse Reactions – Melanoma or NSCLC
Action Recommended Dose

First Dose Reduction
300 mg (four 75 mg capsules) orally once daily

Second Dose Reduction
225 mg (three 75 mg capsules) orally once daily

Subsequent Modification
Permanently discontinue if unable to tolerate BRAFTOVI 225 mg (three 75 mg capsules) once daily


BRAF V600E Mutation-Positive Metastatic Colorectal Cancer (CRC)

If cetuximab is discontinued, discontinue BRAFTOVI.

Dose reductions for adverse reactions associated with BRAFTOVI are presented in Table 2.
Table 2: Recommended Dose Reductions for BRAFTOVI for Adverse Reactions – CRC
Action Recommended Dose

First Dose Reduction
225 mg (three 75 mg capsules) orally once daily

Second Dose Reduction
150 mg (two 75 mg capsules) orally once daily

Subsequent Modification
Permanently discontinue if unable to tolerate BRAFTOVI 150 mg (two 75 mg capsules) once daily


BRAF V600E or V600K Mutation-Positive Unresectable or Metastatic Melanoma, BRAF V600E Mutation-Positive Metastatic Colorectal Cancer (CRC), or BRAF V600E Mutation-Positive NSCLC

Dosage modifications for adverse reactions associated with BRAFTOVI are presented in Table 3.
Symptomatic congestive heart failure or absolute decrease in LVEF of greater than 20% from baseline that is also below LLNIf LVEF improves to at least institutional LLN and absolute decrease to less than or equal to 10% compared to baseline, continue BRAFTOVI at the reduced dose [see Dosage and Administration (2.3)].
    • If no improvement, withhold BRAFTOVI until improves to at least institutional LLN and absolute decrease to less than or equal to 10% compared to baseline and then resume at the reduced dose or reduce dose an additional dose level. Grade 2 AST or ALT increased If no improvement within 4 weeks, withhold BRAFTOVI until improves to Grade 0-1 or to pretreatment/baseline levels and then resume at same dose. Grade 3 or 4 AST or ALT increased Grade 1–3 If improved, resume at same or reduced dose.
    • If not improved, permanently discontinue BRAFTOVI. Grade 4 QTcF greater than 500 ms and less than or equal to 60 ms increase from baseline If more than one recurrence, permanently discontinue BRAFTOVI. QTcF greater than 500 ms and greater than 60 ms increase from baseline Grade 2 Grade 3 Grade 4 Recurrent Grade 2 or
    • First occurrence of any Grade 3 If improves to Grade 0–1 or to pretreatment/baseline level, resume at reduced dose.
    • If no improvement, permanently discontinue BRAFTOVI. First occurrence of any Grade 4 If improves to Grade 0–1 or to pretreatment/baseline level, then resume at reduced dose.
    • If no improvement, permanently discontinue BRAFTOVI. Recurrent Grade 3 Recurrent Grade 4
    Table 3: Recommended Dosage Modifications for BRAFTOVI for Adverse Reactions
    Severity of Adverse Reaction National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) version 4.03. Dose Modification for BRAFTOVI

    New Primary Malignancies [see Warnings and Precautions (5.1)]

    Non-Cutaneous RAS Mutation-positive Malignancies
    Permanently discontinue BRAFTOVI.

    Cardiomyopathy [see Warnings and Precautions (5.3)]
    •

    Reduce BRAFTOVI by one dose level [see Dosage and Administration (2.3)].
    ••

    Hepatotoxicity [see Warnings and Precautions (5.4)]
    •

    Maintain BRAFTOVI dose.
    •
    •

    See  Other Adverse Reactions.

    Uveitis [see Warnings and Precautions (5.6) ]
    •

    If Grade 1 or 2 does not respond to specific ocular therapy, or for Grade 3 uveitis, withhold BRAFTOVI for up to 6 weeks.
    ••
    •

    Permanently discontinue BRAFTOVI.

    QTc Prolongation [see Warnings and Precautions (5.7) ]
    •

    Withhold BRAFTOVI until QTcF less than or equal to 500 ms. Resume at reduced dose.
    •
    •

    Permanently discontinue BRAFTOVI.

    Dermatologic [other than Hand-foot Skin Reaction (HFSR)] [see Adverse Reactions (6.1)]
    •

    If no improvement within 2 weeks, withhold BRAFTOVI until Grade 0–1. Resume at same dose.
    •

    Withhold BRAFTOVI until Grade 0–1. Resume at same dose if first occurrence or reduce dose if recurrent.
    •

    Permanently discontinue BRAFTOVI.
    Other Adverse Reactions (including Hemorrhage) [see Warnings and Precautions (5)] and HFSR [see Adverse Reactions (6.1)] Dose modification of BRAFTOVI when administered with binimetinib or with cetuximab is not recommended for new primary cutaneous malignancies; ocular events other than uveitis, iritis, and iridocyclitis; interstitial lung disease/pneumonitis; creatine phosphokinase (CPK) elevation; rhabdomyolysis; and venous thromboembolism.
    ••

    Withhold BRAFTOVI for up to 4 weeks.
    ••
    •

    Permanently discontinue BRAFTOVI orWithhold BRAFTOVI for up to 4 weeks.
    ••
    •

    Consider permanently discontinuing BRAFTOVI.
    •

    Permanently discontinue BRAFTOVI.

    Refer to the binimetinib or cetuximab prescribing information for dose modifications for adverse reactions associated with each product, as appropriate.

    2.6 Dose Modifications for Coadministration With Strong or Moderate CYP3A4 Inhibitors


    Avoid coadministration of BRAFTOVI with strong or moderate CYP3A4 inhibitors. If coadministration is unavoidable, reduce the BRAFTOVI dose according to the recommendations in Table 4. After the inhibitor has been discontinued for 3 to 5 elimination half-lives, resume the BRAFTOVI dose that was taken prior to initiating the CYP3A4 inhibitor [see Drug Interactions (7.1), Clinical Pharmacology (12.3)]    .
    Table 4: Recommended Dose Reductions for BRAFTOVI for Coadministration With Strong or Moderate CYP3A4 Inhibitors
    Current Daily Dose Current daily dose refers to recommended dose of BRAFTOVI based on indication or reductions for adverse reactions based on dosing recommendations in Table 1 (Melanoma) and Table 2 (CRC). Dose for Coadministration with Moderate CYP3A4 Inhibitor Dose for Coadministration with Strong CYP3A4 Inhibitor

    450 mg
    225 mg (three 75 mg capsules)
    150 mg (two 75 mg capsules)

    300 mg
    150 mg (two 75 mg capsules)
    75 mg

    225 mg
    75 mg
    75 mg

    150 mg
    75 mg
    75 mgEncorafenib exposure at the 75 mg QD BRAFTOVI dosage when coadministered with a strong CYP3A4 inhibitor is expected to be higher than at the 150 mg QD dosage in the absence of a CYP3A4 inhibitor and similar to exposure at the 225 mg QD dosage in the absence of a CYP3A4 inhibitor. Monitor patients closely for adverse reactions and use clinical judgement when using BRAFTOVI with strong CYP3A4 inhibitors at the 150 mg dose level.

    3 Dosage Forms And Strengths


    Capsules: 75 mg, hard gelatin, stylized "A" on beige cap and "LGX 75mg" on white body.


    Capsules: 75 mg. (3)

    4 Contraindications


    None.


    None. (4)

    5 Warnings And Precautions


    • • New Primary Malignancies, cutaneous and non-cutaneous: Can occur. Monitor for malignancies and perform dermatologic evaluations prior to, while on therapy, and following discontinuation of treatment. (5.1)
    • • Tumor Promotion in BRAF Wild-Type Tumors: Increased cell proliferation can occur with BRAF inhibitors. (5.2)
    • • Cardiomyopathy: Assess left ventricular ejection fraction (LVEF) before initiating treatment with BRAFTOVI and binimetinib, and after one month of treatment, then every 2 to 3 months thereafter. The safety of BRAFTOVI in combination with binimetinib has not been established in patients with LVEF below 50%. (5.3)
    • • Hepatotoxicity: Monitor liver function tests before and during treatment with BRAFTOVI and binimetinib and as clinically indicated. (5.4)
    • • Hemorrhage: Major hemorrhagic events can occur in patients receiving BRAFTOVI and binimetinib. (5.5)
    • • Uveitis: Perform ophthalmologic evaluation at regular intervals and for any visual disturbances. (5.6)
    • • QT Prolongation: Monitor electrolytes before and during treatment. Correct electrolyte abnormalities and control for cardiac risk factors for QT prolongation. Withhold BRAFTOVI for QTc of 500 ms or greater. (5.7)
    • • Embryo-Fetal Toxicity: Can cause fetal harm. Advise females with reproductive potential of potential risk to the fetus and to use effective non-hormonal method of contraception. (5.8, 8.1, 8.3)
    • • Risks Associated with BRAFTOVI as a Single Agent: If binimetinib is temporarily interrupted or permanently discontinued, reduce the dose of BRAFTOVI as recommended. (5.9)
    • • Risks Associated with Combination Treatment: BRAFTOVI is indicated for use as part of a regimen in combination with binimetinib or cetuximab. (5.10)

    5.1 New Primary Malignancies


    New primary malignancies, cutaneous and non-cutaneous, have been observed in patients treated with BRAF inhibitors and can occur with BRAFTOVI.


    Cutaneous Malignancies

    In COLUMBUS, cutaneous squamous cell carcinoma (cuSCC), including keratoacanthoma (KA), occurred in 2.6%, and basal cell carcinoma occurred in 1.6% of patients who received BRAFTOVI in combination with binimetinib. Median time to first occurrence of cuSCC/KA was 5.8 months (range 1 to 9 months) [see Adverse Reactions (6.1)].

    For patients who received BRAFTOVI as a single agent, cuSCC/KA was reported in 8%, basal cell carcinoma in 1%, and a new primary melanoma in 5% of patients.

    In BEACON CRC, cuSCC/KA occurred in 1.4% of patients with CRC, and a new primary melanoma occurred in 1.4% of patients who received BRAFTOVI in combination with cetuximab.

    In PHAROS, cuSCC and skin papilloma, each occurred in 2% of patients who received BRAFTOVI in combination with binimetinib.

    Perform dermatologic evaluations prior to initiating treatment, every 2 months during treatment, and for up to 6 months following discontinuation of treatment. Manage suspicious skin lesions with excision and dermatopathologic evaluation. Dose modification is not recommended for new primary cutaneous malignancies.


    Non-Cutaneous Malignancies

    Based on its mechanism of action, BRAFTOVI may promote malignancies associated with activation of RAS through mutation or other mechanisms [see Warnings and Precautions (5.2)]. Monitor patients receiving BRAFTOVI for signs and symptoms of non-cutaneous malignancies. Discontinue BRAFTOVI for RAS mutation-positive non-cutaneous malignancies [see Dosage and Administration (2.5)].

    5.2 Tumor Promotion in BRAF Wild-Type Tumors


    In vitro experiments have demonstrated paradoxical activation of MAP-kinase signaling and increased cell proliferation in BRAF wild-type cells, which are exposed to BRAF inhibitors. Confirm evidence of BRAF V600E or V600K mutation prior to initiating BRAFTOVI [see Indications and Usage (1), Dosage and Administration (2.1)].

    5.3 Cardiomyopathy


    Cardiomyopathy, manifesting as left ventricular dysfunction associated with symptomatic or asymptomatic decreases in ejection fraction, has been reported in patients treated with BRAFTOVI in combination with binimetinib. In COLUMBUS, evidence of cardiomyopathy (decreased in LVEF below the institutional LLN with an absolute decreased in LVEF ≥10% below baseline as detected by echocardiography or MUGA) occurred in 7% of patients receiving BRAFTOVI plus binimetinib. Grade 3 left ventricular dysfunction occurred in 1.6% of patients. The median time to first occurrence of left ventricular dysfunction (any grade) in patients receiving BRAFTOVI in combination with binimetinib was 3.6 months (range 0 to 21 months). Cardiomyopathy resolved in 87% of patients receiving BRAFTOVI plus binimetinib.

    In PHAROS, evidence of cardiomyopathy (decrease in LVEF below the institutional LLN with an absolute decrease in LVEF ≥10% below baseline as detected by echocardiography or MUGA) occurred in 11% of patients receiving BRAFTOVI in combination with binimetinib. Grade 3 left ventricular dysfunction occurred in 1% of patients. Cardiomyopathy resolved in 82% of patients receiving BRAFTOVI plus binimetinib.

    Assess ejection fraction by echocardiogram or MUGA scan prior to initiating treatment, one month after initiating treatment, and every 2 to 3 months during treatment. The safety of BRAFTOVI in combination with binimetinib has not been established in patients with baseline ejection fraction that is either below 50% or below the institutional lower limit of normal (LLN). Patients with cardiovascular risk factors should be monitored closely when treated with BRAFTOVI.

    Withhold, reduce dose, or permanently discontinue based on severity of adverse reaction [see Dosage and Administration (2.3), Adverse Reactions (6.1)].

    5.4 Hepatotoxicity


    Hepatotoxicity can occur when BRAFTOVI is administered in combination with binimetinib. In COLUMBUS, the incidence of Grade 3 or 4 increases in liver function laboratory tests in patients receiving BRAFTOVI in combination with binimetinib was 6% for alanine aminotransferase (ALT), 2.6% for aspartate aminotransferase (AST), and 0.5% for alkaline phosphatase. In PHAROS, the incidence of Grade 3 or 4 increases in liver function laboratory tests in patients receiving BRAFTOVI in combination with binimetinib was 10% for AST, 9% for ALT, and 3.2% for alkaline phosphatase.

    Monitor liver laboratory tests before initiation of BRAFTOVI, monthly during treatment, and as clinically indicated. Withhold, reduce dose, or permanently discontinue based on severity of adverse reaction [see Dosage and Administration (2.3), Adverse Reactions (6.1)].

    5.5 Hemorrhage


    In COLUMBUS, hemorrhage occurred in 19% of patients receiving BRAFTOVI in combination with binimetinib; Grade 3 or greater hemorrhage occurred in 3.2% of patients. The most frequent hemorrhagic events were gastrointestinal, including rectal hemorrhage (4.2%), hematochezia (3.1%), and hemorrhoidal hemorrhage (1%). Fatal intracranial hemorrhage in the setting of new or progressive brain metastases occurred in 1.6% of patients.

    In BEACON CRC, hemorrhage occurred in 19% of patients receiving BRAFTOVI in combination with cetuximab; Grade 3 or higher hemorrhage occurred in 1.9% of patients, including fatal gastrointestinal hemorrhage in 0.5% of patients. The most frequent hemorrhagic events were epistaxis (6.9%), hematochezia (2.3%), and rectal hemorrhage (2.3%).

    In PHAROS, hemorrhage occurred in 12% of patients receiving BRAFTOVI in combination with binimetinib including fatal hemorrhage intracranial (1%); Grade 3 or 4 hemorrhage occurred in 4.1% of patients. The most frequent hemorrhagic events were anal hemorrhage and hemothorax (2% each).

    Withhold, reduce dose, or permanently discontinue based on severity of adverse reaction [see Dosage and Administration (2.5), Adverse Reactions (6.1)].

    5.6 Uveitis


    Uveitis, including iritis and iridocyclitis, has been reported in patients treated with BRAFTOVI in combination with binimetinib. In COLUMBUS, the incidence of uveitis among patients treated with BRAFTOVI in combination with binimetinib was 4%. In PHAROS, the incidence of uveitis among patients treated with BRAFTOVI in combination with binimetinib was 1%.

    Assess for visual symptoms at each visit. Perform an ophthalmologic evaluation at regular intervals and for new or worsening visual disturbances, and to follow new or persistent ophthalmologic findings. Withhold, reduce dose, or permanently discontinue based on severity of adverse reaction [see Dosage and Administration (2.5), Adverse Reactions (6.1)].

    5.7 QT Prolongation


    BRAFTOVI is associated with dose-dependent QTc interval prolongation in some patients [see Clinical Pharmacology (12.2)]. In COLUMBUS, an increase in QTcF to >500 ms was measured in 0.5% (1/192) of patients who received BRAFTOVI in combination with binimetinib. In PHAROS, an increase in QTcF to >500 ms was measured in 2.1% (2/95) of patients who received BRAFTOVI in combination with binimetinib.

    Monitor patients who already have or who are at significant risk of developing QTc prolongation, including patients with known long QT syndromes, clinically significant bradyarrhythmias, severe or uncontrolled heart failure and those taking other medicinal products associated with QT prolongation. Correct hypokalemia and hypomagnesemia prior to and during BRAFTOVI administration. Withhold, reduce dose, or permanently discontinue for QTc >500 ms [see Dosage and Administration (2.5), Adverse Reactions (6.1)].

    5.8 Embryo-Fetal Toxicity


    Based on its mechanism of action, BRAFTOVI can cause fetal harm when administered to a pregnant woman. Encorafenib produced embryo-fetal developmental changes in rats and rabbits and was an abortifacient in rabbits at doses greater than or equal to those resulting in exposures approximately 26 (in the rat) and 178 (in the rabbit) times the human exposure at the recommended dose of 450 mg, with no clear findings at lower doses.

    Advise pregnant women and females of reproductive potential of the potential risk to a fetus. Advise females of reproductive potential to use an effective, non-hormonal method of contraception since BRAFTOVI can render hormonal contraceptives ineffective, during treatment and for 2 weeks after the last dose of BRAFTOVI [see Use in Specific Populations (8.1, 8.3)].

    5.9 Risks Associated with BRAFTOVI as a Single Agent


    BRAFTOVI when used as a single agent is associated with an increased risk of certain adverse reactions compared to when BRAFTOVI is used in combination with binimetinib. In COLUMBUS, Grades 3 or 4 dermatologic reactions occurred in 21% of patients treated with BRAFTOVI single agent compared to 2% of patients treated with BRAFTOVI in combination with binimetinib [see Warnings and Precautions (5.1), Adverse Reactions (6.1)].

    If binimetinib is temporarily interrupted or permanently discontinued, reduce the dose of BRAFTOVI as recommended [see Dosage and Administration (2.5)].

    5.10 Risks Associated with Combination Treatment


    BRAFTOVI is indicated for use as part of a regimen in combination with binimetinib or cetuximab. Refer to the prescribing information for binimetinib and cetuximab for additional risk information.

    6 Adverse Reactions


    The following adverse reactions are described elsewhere in the labeling:


    Melanoma: Most common adverse reactions (≥25%) for BRAFTOVI, in combination with binimetinib, are fatigue, nausea, vomiting, abdominal pain, and arthralgia. (6.1)

    CRC: Most common adverse reactions (≥25%) for BRAFTOVI, in combination with cetuximab, are fatigue, nausea, diarrhea, dermatitis acneiform, abdominal pain, decreased appetite, arthralgia, and rash. (6.1)

    NSCLC: Most common adverse reactions (≥25%) for BRAFTOVI, in combination with binimetinib, are fatigue, nausea, diarrhea, musculoskeletal pain, vomiting, abdominal pain, visual impairment, constipation, dyspnea, rash, and cough. (6.1)

     

    To report SUSPECTED ADVERSE REACTIONS, contact Pfizer Inc. at 1-800-438-1985 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

    6.1 Clinical Trials Experience


    Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.


    BRAF V600E or V600K Mutation-Positive Unresectable or Metastatic Melanoma

    The safety of BRAFTOVI in combination with binimetinib is described in 192 patients with BRAF V600 mutation-positive unresectable or metastatic melanoma who received BRAFTOVI (450 mg once daily) in combination with binimetinib (45 mg twice daily) in a randomized open-label, active-controlled trial (COLUMBUS).

    The COLUMBUS trial [see Clinical Studies (14.1)] excluded patients with a history of Gilbert's syndrome, abnormal left ventricular ejection fraction, prolonged QTc (>480 ms), uncontrolled hypertension, and history or current evidence of retinal vein occlusion. The median duration of exposure was 11.8 months for patients treated with BRAFTOVI in combination with binimetinib and 6.2 months for patients treated with vemurafenib.

    The most common (≥25%) adverse reactions in patients receiving BRAFTOVI in combination with binimetinib were fatigue, nausea, vomiting, abdominal pain, and arthralgia.

    Adverse reactions leading to dose interruptions of BRAFTOVI occurred in 30% of patients receiving BRAFTOVI in combination with binimetinib; the most common were nausea (7%), vomiting (7%), and pyrexia (4%). Adverse reactions leading to dose reductions of BRAFTOVI occurred in 14% of patients receiving BRAFTOVI in combination with binimetinib; the most common were arthralgia (2%), fatigue (2%), and nausea (2%). Five percent (5%) of patients receiving BRAFTOVI in combination with binimetinib experienced an adverse reaction that resulted in permanent discontinuation of BRAFTOVI; the most common were hemorrhage in 2% and headache in 1% of patients.

    Table 5 and Table 6 present adverse drug reactions and laboratory abnormalities, respectively, identified in COLUMBUS. The COLUMBUS trial was not designed to demonstrate a statistically significant difference in adverse reaction rates for BRAFTOVI in combination with binimetinib, as compared to vemurafenib, for any specific adverse reaction uled in Table 5.
    Table 5: Adverse Reactions Occurring in ≥10% of Patients Receiving BRAFTOVI in Combination With Binimetinib in COLUMBUSGrades per National Cancer Institute CTCAE v4.03.
    Adverse Reaction BRAFTOVI with binimetinib N=192 Vemurafenib N=186
    All Grades (%) Grades 3 and 4 Grade 4 adverse reactions limited to fatigue (n=1), pruritus (n=1), and rash (n=1) in the BRAFTOVI with binimetinib arm. (%) All Grades (%) Grades 3 and 4 (%)

    General Disorders and Administration Site Conditions

      FatigueRepresents a composite of multiple, related preferred terms.

    43
    3
    46
    6

      Pyrexia

    18
    4
    30
    0

    Gastrointestinal Disorders

      Nausea
    41
    2
    34
    2

      Vomiting

    30
    2
    16
    1

      Abdominal pain

    28
    4
    16
    1

      Constipation
    22
    0
    6
    1

    Musculoskeletal and Connective Tissue Disorders

      Arthralgia

    26
    1
    46
    6

      Myopathy

    23
    0
    22
    1

      Pain in extremity
    11
    1
    13
    1

    Skin and Subcutaneous Tissue Disorders

      Hyperkeratosis

    23
    1
    49
    1

      Rash

    22
    1
    53
    13

      Dry skin

    16
    0
    26
    0

      Alopecia

    14
    0
    38
    0

      Pruritus

    13
    1
    21
    1

    Nervous System Disorders

      Headache

    22
    2
    20
    1

      Dizziness

    15
    3
    4
    0

      Peripheral neuropathy

    12
    1
    13
    2

    Vascular Disorders

      Hemorrhage

    19
    3
    9
    2

    BRAFTOVI when used as a single agent increases the risk of certain adverse reactions compared to BRAFTOVI in combination with binimetinib. In patients receiving BRAFTOVI 300 mg orally once daily as a single agent, the following adverse reactions were observed at a higher rate (≥5%) compared to patients receiving BRAFTOVI in combination with binimetinib: palmar-plantar erythrodysesthesia syndrome (51% vs. 7%), hyperkeratosis (57% vs. 23%), dry skin (38% vs. 16%), erythema (16% vs. 7%), rash (41% vs. 22%), alopecia (56% vs. 14%), pruritus (31% vs. 13%), arthralgia (44% vs. 26%), myopathy (33% vs. 23%), back pain (15% vs. 9%), dysgeusia (13% vs. 6%), and acneiform dermatitis (8% vs. 3%).

    Other clinically important adverse reactions occurring in <10% of patients who received BRAFTOVI in combination with binimetinib were:

    Nervous system disorders: Facial paresis

    Gastrointestinal disorders: Pancreatitis

    Skin and subcutaneous tissue disorders: Panniculitis

    Immune system disorders: Drug hypersensitivity
    Table 6: Laboratory Abnormalities Occurring in ≥10% (All Grades) of Patients Receiving BRAFTOVI in Combination With Binimetinib in COLUMBUSGrades per National Cancer Institute CTCAE v4.03.
    Laboratory Abnormality BRAFTOVI with binimetinib N=192 Vemurafenib N=186
    All Grades (%) Grades 3 and 4 (%) All Grades (%) Grades 3 and 4 (%)

    Hematology

      Anemia
    36
    3.6
    34
    2.2

      Leukopenia
    13
    0
    10
    0.5

      Lymphopenia
    13
    2.1
    30
    7

      Neutropenia
    13
    3.1
    4.8
    0.5

    Chemistry

      Increased Creatinine
    93
    3.6
    92
    1.1

      Increased Gamma Glutamyl Transferase
    45
    11
    34
    4.8

      Increased ALT
    29
    6
    27
    2.2

      Increased AST
    27
    2.6
    24
    1.6

      Hyperglycemia
    28
    5
    20
    2.7

      Increased Alkaline Phosphatase
    21
    0.5
    35
    2.2

      Hyponatremia
    18
    3.6
    15
    0.5

      Hypermagnesemia
    10
    1.0
    26
    0.5


    BRAF V600E Mutation-Positive Metastatic Colorectal Cancer (CRC)

    The safety of BRAFTOVI 300 mg once daily in combination with cetuximab (400 mg/m2 initial dose, followed by 250 mg/m2 weekly) was evaluated in 216 patients with BRAF V600E mutation-positive metastatic CRC in a randomized, open-label, active-controlled trial (BEACON CRC). The BEACON CRC trial [see Clinical Studies (14.2)] excluded patients with a history of Gilbert's syndrome, abnormal left ventricular ejection fraction, prolonged QTc (>480 ms), uncontrolled hypertension, and history or current evidence of retinal vein occlusion. The median duration of exposure was 4.4 months for patients treated with BRAFTOVI in combination with cetuximab and 1.6 months for patients treated with either irinotecan or infusional 5-fluorouracil (5-FU)/folinic acid (FA)/irinotecan (FOLFIRI) in combination with cetuximab.

    The most common (≥25%) adverse reactions in patients receiving BRAFTOVI in combination with cetuximab were fatigue, nausea, diarrhea, dermatitis acneiform, abdominal pain, decreased appetite, arthralgia, and rash.

    Adverse reactions leading to dose interruptions of BRAFTOVI occurred in 33% of patients receiving BRAFTOVI in combination with cetuximab; the most common were vomiting (4%), fatigue (4%), nausea (4%), pyrexia (3%), and diarrhea (3%). Adverse reactions leading to dose reductions of BRAFTOVI occurred in 9% of patients receiving BRAFTOVI in combination with cetuximab; the most common were fatigue (2%), arthralgia (2%), and peripheral neuropathy (2%). Ten percent (10%) of patients receiving BRAFTOVI in combination with cetuximab experienced an adverse reaction that resulted in permanent discontinuation of BRAFTOVI. None of the adverse reactions leading to permanent discontinuation of BRAFTOVI occurred in more than one patient (>0.5%).

    Table 7 and Table 8 present adverse drug reactions and laboratory abnormalities, respectively, identified in BEACON CRC.
    Table 7: Adverse Reactions Occurring in ≥10% of Patients Receiving BRAFTOVI in Combination With Cetuximab in BEACON CRCGrades per National Cancer Institute CTCAE v4.03.
    Adverse Reaction BRAFTOVI with cetuximab N=216 Irinotecan with cetuximab or FOLFIRI with cetuximab N=193
    All Grades (%) ≥ Grade 3 Grade 4-5 adverse reactions in the BRAFTOVI with cetuximab arm were limited to Grade 5 hemorrhage (n=1). (%) All Grades (%) ≥ Grade 3 (%)

    General Disorders and Administration Site Conditions

      FatigueRepresents a composite of multiple, related preferred terms.

    51
    7
    50
    8

      Pyrexia

    17
    1
    15
    1

    Gastrointestinal Disorders

      Nausea
    34
    1
    41
    1

      Diarrhea

    33
    2
    48
    10

      Abdominal pain

    30
    4
    32
    5

      Vomiting
    21
    1
    29
    3

      Constipation
    15
    0
    18
    1

    Metabolism and Nutrition Disorders

      Decreased appetite
    27
    1
    27
    3

    Musculoskeletal and Connective Tissue Disorders

      Arthralgia

    27
    1
    3
    0

      Myopathy

    15
    1
    4
    0

      Pain in extremity
    10
    0
    1
    0

    Skin and Subcutaneous Tissue Disorders

      Dermatitis acneiform

    32
    1
    43
    3

      Rash

    26
    0
    26
    2

      Pruritus

    14
    0
    6
    0

      Melanocytic nevus
    14
    0
    0
    0

      Dry skin

    13
    0
    12
    1

    Nervous System Disorders

      Headache

    20
    0
    3
    0

      Peripheral neuropathy

    12
    1
    6
    0

    Vascular Disorders

      Hemorrhage

    19
    2
    9
    0

    Psychiatric Disorders

      Insomnia

    13
    0
    6
    0

    Other clinically important adverse reactions occurring in <10% of patients who received BRAFTOVI in combination with cetuximab were:

    Gastrointestinal disorders: Pancreatitis
    Table 8: Laboratory Abnormalities Occurring in ≥10% (All Grades) of Patients Receiving BRAFTOVI in Combination With Cetuximab in BEACON CRCGrades per National Cancer Institute CTCAE v4.03.
    Laboratory Abnormality Based on the number of patients with available baseline and at least one on-treatment laboratory test. BRAFTOVI with cetuximab Irinotecan with cetuximab or FOLFIRI with cetuximab
    All Grades (%) Grades 3 and 4 (%) All Grades (%) Grades 3 and 4 (%)

    Hematology

      Anemia
    34
    4
    48
    5

      Lymphopenia
    24
    7
    35
    5

      Increased Activated Partial Thromboplastin Time
    13
    1
    7
    1

    Chemistry

      Hypomagnesemia
    19
    0
    22
    1

      Increased Alkaline Phosphatase
    18
    4
    30
    7

      Increased ALT
    17
    0
    29
    3

      Increased AST
    15
    1
    22
    2

      Hypokalemia
    12
    3
    32
    5

      Hyponatremia
    11
    2
    13
    2

    BRAF V600E Mutation-Positive Metastatic Non-Small Cell Lung Cancer (NSCLC)

    The safety of BRAFTOVI in combination with binimetinib was evaluated in 98 patients with BRAF V600E mutation-positive metastatic NSCLC who received BRAFTOVI (450 mg once daily) in combination with binimetinib (45 mg twice daily) in an open-label, single-arm trial (PHAROS).

    The PHAROS trial [see Clinical Studies (14.3)] excluded patients with abnormal left ventricular ejection fraction, prolonged QTc (>480 ms), uncontrolled hypertension, and history or current evidence of retinal vein occlusion. The median duration of treatment for BRAFTOVI and binimetinib was 9.2 and 8.4 months, respectively.

    The most common (≥25%) adverse reactions in patients receiving BRAFTOVI were fatigue, nausea, diarrhea, musculoskeletal pain, vomiting, abdominal pain, visual impairment, constipation, dyspnea, rash, and cough.

    Adverse reactions leading to dose interruptions of BRAFTOVI occurred in 59% of patients receiving BRAFTOVI; the most common (≥5%) were diarrhea (17%); nausea (13%); musculoskeletal pain, fatigue (8% each); AST increased (7%); ALT increased, anemia, hemorrhage, vomiting (6% each); and acute kidney injury (5%). Adverse reactions leading to dose reductions of BRAFTOVI occurred in 30% of patients receiving BRAFTOVI; the most common (≥5%) were diarrhea, nausea (8% each); AST increased and fatigue (5% each). A total of 16% of patients receiving BRAFTOVI experienced an adverse reaction that resulted in permanent discontinuation of BRAFTOVI; the most common (≥2%) were diarrhea, musculoskeletal pain (3.1% each); fatigue, rash, nausea, visual impairment, and vomiting (2% each). None of the other adverse reactions leading to permanent discontinuation of BRAFTOVI occurred in more than 1 patient.

    Serious adverse reactions occurred in 38% of patients who received BRAFTOVI in combination with binimetinib. Serious adverse reactions occurring in ≥2% of patients were hemorrhage (6%); diarrhea (4.1%); anemia, dyspnea, pneumonia (3.1% each); arrhythmia, device related infection, edema, myocardial infarction, and pleural effusion (2% each). Fatal adverse reactions occurred in 2% of patients who received BRAFTOVI (450 mg once daily) in combination with binimetinib, including intracranial hemorrhage and myocardial infarction (1% each).

    Table 9 and Table 10 present adverse drug reactions and laboratory abnormalities, respectively, identified in PHAROS.
    Table 9: Adverse Reactions Occurring in ≥10% of Patients Receiving BRAFTOVI in Combination with Binimetinib in PHAROSGrades per National Cancer Institute CTCAE v4.03.

    Adverse Reaction

    BRAFTOVI

    with binimetinib N=98

    All

    Grades

    (%)

    Grades 3 and 4 One Grade 5 adverse reaction of hemorrhage occurred.

    (%)

    General Disorders and Administration Site Conditions

      FatigueFatigue includes fatigue, asthenia.

    61
    8

      EdemaEdema includes edema peripheral, generalized edema, swelling, localized edema, face edema.

    23
    1

      Pyrexia
    22
    0

    Gastrointestinal Disorders

      Nausea
    58
    3.1

      DiarrheaDiarrhea includes diarrhea, colitis.

    52
    7

      Vomiting
    37
    1

      Abdominal painAbdominal pain includes abdominal pain, abdominal pain upper, abdominal discomfort, epigastric discomfort.

    32
    1

      Constipation
    27
    0

    Eye Disorders

      Visual impairmentVisual impairment includes vision blurred, visual impairment, vitreous floaters, photophobia, visual acuity reduced, photopsia.

    29
    2

    Musculoskeletal and Connective Tissue Disorders

      Musculoskeletal painMusculoskeletal pain includes back pain, arthralgia, pain in extremity, myalgia, musculoskeletal chest pain, non-cardiac chest pain, neck pain.

    48
    4.1

    Skin and Subcutaneous Tissue Disorders

      RashRash includes rash, rash macular, rash maculo-papular, rash papular, rash pustular, dermatitis acneiform, palmar-plantar erythrodysesthesia syndrome, eczema, skin exfoliation.

    27
    3.1

      PruritisPruritis includes pruritus, pruritus genital.

    16
    0

      Dry skin
    13
    0

      Alopecia
    12
    0

    Respiratory, Thoracic and Mediastinal Disorders

      DyspneaDyspnea includes dyspnea, dyspnea exertional.

    27
    8

      CoughCough includes cough, productive cough.

    26
    0

    Nervous System Disorders

      DizzinessDizziness includes dizziness, balance disorder.

    17
    1

      Headache
    11
    0

    Metabolism and Nutrition Disorders

      Decreased appetite
    14
    1

    Vascular Disorders

      Hemorrhage Hemorrhage includes anal hemorrhage, hemothorax, gastrointestinal hemorrhage, hematochezia, hematuria, hemoptysis, hemorrhage intracranial, hyphema, small intestinal hemorrhage, upper gastrointestinal hemorrhage, vaginal hemorrhage.

    12
    4.1

      Hypertension
    10
    5

    Cardiac Disorders

      Left ventricular dysfunction/cardiomyopathyLeft ventricular dysfunction/cardiomyopathy includes ejection fraction decreased, cardiac failure, cardiac failure congestive.

    11
    1

    Investigations

      Weight increased
    11
    1

    Psychiatric Disorders

      Insomnia
    10
    0

    Other clinically important adverse reactions occurring in <10% of patients who received BRAFTOVI in combination with binimetinib were:

    Nervous system disorders: Peripheral neuropathy, Dysgeusia, Facial paresis

    Gastrointestinal disorders: Pancreatitis

    Skin and subcutaneous tissue disorders: Hyperkeratosis, Erythema

    Immune system disorders: Drug hypersensitivity
    Table 10: Laboratory Abnormalities Occurring in ≥10% (All Grades) of Patients Receiving BRAFTOVI with BinimetinibGrades per National Cancer Institute CTCAE v4.03.

     

    Laboratory Abnormality Based on the number of patients with available baseline and at least one on-treatment laboratory test.

    BRAFTOVI with binimetinib

    All

    Grades

    (%)

    Grades

    3 and 4

    (%)

    Hematology

       Anemia
    47
    11

       Lymphopenia
    24
    6

       Thrombocytopenia
    20
    1.1

       Leukopenia
    12
    0

       Neutropenia
    12
    1.1

    Chemistry

       Increased creatinine
    91
    3.2

       Hyperglycemia
    48
    6

       Increased creatine kinase
    41
    3.3

       Lipase increased
    40
    14

       Increased ALT
    34
    9

       Hypoalbuminemia
    32
    0

       Increased AST
    31
    10

       Increased alkaline phosphatase
    31
    3.2

       Hyperkalemia
    31
    2.1

       Hyponatremia
    26
    11

       Serum amylase increased
    22
    1.1

       Hypocalcemia
    12
    2.1

    7 Drug Interactions


    • •Strong or moderate CYP3A4 inhibitors: Avoid coadministration. If unavoidable, reduce BRAFTOVI dosage. (2.6, 7.1)
    • •Strong CYP3A4 inducers: Avoid coadministration. (7.1)
    • •Sensitive CYP3A4 substrates: Avoid coadministration with CYP3A4 substrates (including hormonal contraceptives) for which a decrease in plasma concentration may lead to reduced efficacy of the substrate. (7.2)
    • •Transporters: Dose reductions of drugs that are substrates of OATP1B1, OATP1B3, or BCRP may be required when used concomitantly with BRAFTOVI. (7.2, 12.3)

    7.1 Effect of Other Drugs on BRAFTOVI


    Strong or Moderate CYP3A4 Inhibitors

    Coadministration of BRAFTOVI with a strong or moderate CYP3A4 inhibitor increases encorafenib plasma concentrations [see Clinical Pharmacology (12.3)] and may increase encorafenib adverse reactions. Avoid coadministration of BRAFTOVI with strong or moderate CYP3A4 inhibitors, including grapefruit juice. If coadministration is unavoidable, reduce the BRAFTOVI dose [see Dosage and Administration (2.6)].


    Strong CYP3A4 Inducers

    Coadministration of BRAFTOVI with a strong CYP3A4 inducer may decrease encorafenib plasma concentrations [see Clinical Pharmacology (12.3)] and may decrease encorafenib efficacy. Avoid coadministration of BRAFTOVI with strong CYP3A4 inducers.

    7.2 Effect of BRAFTOVI on Other Drugs



    Sensitive CYP3A4 Substrates

    BRAFTOVI is a strong CYP3A4 inducer at steady-state. Concomitant use of BRAFTOVI may decrease the plasma concentrations of CYP3A4 substrates (including hormonal contraceptives), [see Clinical Pharmacology (12.3)], which may reduce the efficacy of these substrates. Avoid the coadministration of BRAFTOVI with CYP3A4 substrates for which a decrease in plasma concentration may lead to reduced efficacy of the substrate. If the coadministration cannot be avoided, see the CYP3A4 substrate product labeling for recommendations.


    OATP1B1, OATP1B3, or BCRP Substrates

    Coadministration of BRAFTOVI with OATP1B1, OATP1B3, or BCRP substrates can result in increased concentrations of the substrates, and may increase toxicity of these agents. When used in combination, monitor patients closely for signs and symptoms of increased exposure and consider adjusting the dose of these substrates [see Clinical Pharmacology (12.3)].

    7.3 Drugs That Prolong the QT Interval


    BRAFTOVI is associated with dose-dependent QTc interval prolongation [see Warnings and Precautions (5.7) , Clinical Pharmacology (12.2)]. Avoid coadministration of BRAFTOVI with drugs known to prolong the QT/QTc interval.

    8 Use In Specific Populations


    • • Lactation: Advise not to breastfeed. (8.2)
    • • Males of Reproductive Potential: BRAFTOVI may impair fertility. (8.3)

    8.1 Pregnancy


    Risk Summary

    Based on its mechanism of action, BRAFTOVI can cause fetal harm when administered to a pregnant woman [see Clinical Pharmacology (12.1)]. There are no available clinical data on the use of BRAFTOVI during pregnancy. In animal reproduction studies, encorafenib produced embryo-fetal developmental changes in rats and rabbits and was an abortifacient in rabbits at doses greater than or equal to those resulting in exposures approximately 26 (in the rat) and 178 (in the rabbit) times the human exposure at the clinical dose of 450 mg, with no clear findings at lower doses (see Data). Advise pregnant women and females of reproductive potential of the potential risk to a fetus.

    In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively.

    Data


    Animal Data

    In reproductive toxicity studies, administration of encorafenib to rats during the period of organogenesis resulted in maternal toxicity, decreased fetal weights, and increased incidence of total skeletal variations at a dose of 20 mg/kg/day (approximately 26 times the human exposure based on area under the concentration-time curve [AUC] at the recommended clinical dose of 450 mg once daily). In pregnant rabbits, administration of encorafenib during the period of organogenesis resulted in maternal toxicity, decreased fetal body weights, increased incidence of total skeletal variations and increased post-implantation loss, including total loss of pregnancy at a dose of 75 mg/kg/day (approximately 178 times the human exposure based on AUC at the recommended clinical dose of 450 mg once daily). While formal placental transfer studies have not been performed, encorafenib exposure in the fetal plasma of both rats and rabbits was up to 1.7% and 0.8%, respectively, of maternal exposure.

    8.2 Lactation



    Risk Summary

    There are no data on the presence of encorafenib or its metabolites in human milk or the effects of encorafenib on the breastfed child, or the effects on milk production. Because of the potential for serious adverse reactions in a breastfed child from BRAFTOVI, advise women not to breastfeed during treatment with BRAFTOVI and for 2 weeks after the last dose.

    8.3 Females and Males of Reproductive Potential



    BRAFTOVI can cause fetal harm when administered to a pregnant woman [see Use in Specific Populations (8.1)].

    Pregnancy Testing

    Verify the pregnancy status of females of reproductive potential prior to initiating BRAFTOVI [see Use in Specific Populations (8.1)].


    Contraception

    Females

    Advise females of reproductive potential to use effective contraception during treatment with BRAFTOVI and for 2 weeks after the last dose. Counsel patients to use a non-hormonal method of contraception since BRAFTOVI has the potential to render hormonal contraceptives ineffective [see Drug Interactions (7.2)].


    Infertility


    Males

    Based on findings in male rats at doses approximately 13 times the human exposure at the 450 mg clinical dose, use of BRAFTOVI may impact fertility in males [see Nonclinical Toxicology (13.1)].

    8.4 Pediatric Use


    The safety and effectiveness of BRAFTOVI have not been established in pediatric patients.

    8.5 Geriatric Use


    Of the 690 patients with BRAF mutation-positive melanoma who received BRAFTOVI in combination with binimetinib across multiple clinical trials, 20% were aged 65 to 74 years and 8% were aged 75 years and older [see Clinical Studies (14.1)].

    Of the 216 patients with BRAF V600E mutation-positive metastatic CRC who received BRAFTOVI in combination with cetuximab, 62 (29%) were 65 years of age to up to 75 years of age, while 20 (9%) were 75 years of age and over [see Clinical Studies (14.2)].

    Of the 98 patients with BRAF V600E mutation-positive metastatic NSCLC who received BRAFTOVI with binimetinib, 62 (63%) were 65 years of age and over and 20 (20%) were 75 years and over [see Clinical Studies (14.3)].

    No overall differences in the safety or effectiveness of BRAFTOVI plus binimetinib or BRAFTOVI plus cetuximab were observed in older patients as compared to younger patients.

    8.6 Hepatic Impairment


    No BRAFTOVI dosage adjustment is recommended in patients with mild hepatic impairment (Child-Pugh Class A) [see Clinical Pharmacology (12.3)]. A recommended dosage has not been established in patients with moderate (Child-Pugh Class B) or severe (Child-Pugh Class C) hepatic impairment.

    8.7 Renal Impairment


    No BRAFTOVI dosage adjustment is recommended in patients with mild to moderate renal impairment (CLcr 30 to <90 mL/min) [see Clinical Pharmacology (12.3)]. A recommended dosage has not been established in patients with severe renal impairment (CLcr <30 mL/min).

    10 Overdosage


    Since encorafenib is 86% bound to plasma proteins, hemodialysis is likely to be ineffective in the treatment of overdose with BRAFTOVI.

    11 Description


    Encorafenib is a kinase inhibitor. The chemical name is methyl N-{(2S)-1-[(4-{3-[5-chloro-2-fluoro-3-(methanesulfonamido)phenyl]-1-(propan-2-yl)-1H-pyrazol-4-yl}pyrimidin-2-yl)amino]propan-2-yl} carbamate. The molecular formula is C22H27ClFN7O4S and the molecular weight is 540 daltons. The chemical structure of encorafenib is shown below:

    Encorafenib is a white to almost white powder. In aqueous media, encorafenib is slightly soluble at pH 1, very slightly soluble at pH 2, and insoluble at pH 3 and higher.

    BRAFTOVI (encorafenib) capsules for oral use contain 75 mg of encorafenib with the following inactive ingredients: copovidone, poloxamer 188, microcrystalline cellulose, succinic acid, crospovidone, colloidal silicon dioxide, magnesium stearate (vegetable origin). The capsule shell contains gelatin, titanium dioxide, iron oxide red, iron oxide yellow, ferrosoferric oxide, monogramming ink (pharmaceutical glaze, ferrosoferric oxide, propylene glycol).

    12 Clinical Pharmacology


    12.1 Mechanism of Action


    Encorafenib is a kinase inhibitor that targets BRAF V600E, as well as wild-type BRAF and CRAF in in vitro cell-free assays with IC50 values of 0.35, 0.47, and 0.3 nM, respectively. Mutations in the BRAF gene, such as BRAF V600E, can result in constitutively activated BRAF kinases that may stimulate tumor cell growth. Encorafenib was also able to bind to other kinases in vitro including JNK1, JNK2, JNK3, LIMK1, LIMK2, MEK4, and STK36 and reduce ligand binding to these kinases at clinically achievable concentrations (≤0.9 µM).

    Encorafenib inhibited in vitro growth of tumor cell lines expressing BRAF V600 E, D, and K mutations. In mice implanted with tumor cells expressing BRAF V600E, encorafenib induced tumor regressions associated with RAF/MEK/ERK pathway suppression.

    Encorafenib and binimetinib target two different kinases in the RAS/RAF/MEK/ERK pathway. Compared with either drug alone, coadministration of encorafenib and binimetinib resulted in greater anti-proliferative activity in vitro in BRAF mutation-positive cell lines and greater anti-tumor activity with respect to tumor growth inhibition in BRAF V600E mutant human melanoma xenograft studies in mice. Additionally, the combination of encorafenib and binimetinib delayed the emergence of resistance in BRAF V600E mutant human melanoma xenografts in mice compared to either drug alone. In a BRAF V600E mutant NSCLC patient-derived xenograft model in mice, coadministration of encorafenib and binimetinib resulted in greater anti-tumor activity compared to binimetinib alone, with respect to tumor growth inhibition. Increased tumor growth delay after dosing cessation was also observed with the coadmnistration compared to either drug alone.

    In the setting of BRAF-mutant CRC, induction of EGFR-mediated MAPK pathway activation has been identified as a mechanism of resistance to BRAF inhibitors. Combinations of a BRAF inhibitor and agents targeting EGFR have been shown to overcome this resistance mechanism in nonclinical models. Coadministration of encorafenib and cetuximab had an anti-tumor effect greater than either drug alone, in a mouse model of colorectal cancer with mutated BRAF V600E.

    12.2 Pharmacodynamics



    Cardiac Electrophysiology

    A dedicated study to evaluate the QT prolongation potential of BRAFTOVI has not been conducted. BRAFTOVI is associated with dose-dependent QTc interval prolongation. Based on a central tendency analysis of QTc in a study of adult patients with melanoma who received the recommended dose of BRAFTOVI in combination with binimetinib, the largest mean (90% CI) QTcF change from baseline (ΔQTcF) was 18 (14 to 22) ms [see Warnings and Precautions (5.7) ].

    12.3 Pharmacokinetics


    The pharmacokinetics of encorafenib were studied in healthy subjects and patients with solid tumors, including advanced and unresectable or metastatic cutaneous melanoma harboring a BRAF V600E or V600K mutation, BRAF V600E mutation-positive metastatic CRC. After a single dose, systemic exposure of encorafenib was dose proportional over the dose range of 50 mg to 700 mg (0.1 to 1.6 times the maximum recommended dose of 450 mg). After once-daily dosing, systemic exposure of encorafenib was less than dose proportional over the dose range of 50 mg to 800 mg (0.1 to 1.8 times the maximum recommended dose of 450 mg). Steady-state was reached within 15 days, with exposure being 50% lower compared to Day 1; intersubject variability (CV%) of AUC ranged from 12% to 69%.


    Absorption

    The median Tmax of encorafenib is 2 hours. At least 86% of the dose is absorbed.


    Effect of Food

    Following administration of a single dose of BRAFTOVI 100 mg (0.2 times the maximum recommended dose of 450 mg) with a high-fat, high-calorie meal (consisting of approximately 150 calories from protein, 350 calories from carbohydrates, and 500 calories from fat) the mean maximum encorafenib concentration (Cmax) decreased by 36% and there was no effect on AUC.


    Distribution

    The geometric mean (CV%) of apparent volume of distribution is 164 L (70%). The protein binding of encorafenib is 86% in vitro. The blood-to-plasma concentration ratio is 0.58.


    Elimination

    The mean (CV%) terminal half-life (t1/2) of encorafenib is 3.5 hours (17%), and the apparent clearance is 14 L/h (54%) at day 1, increasing to 32 L/h (59%) at steady-state at the maximum recommended dose of 450 mg.


    Metabolism

    Encorafenib is primarily metabolized by CYP3A4 (83%) and to a lesser extent by CYP2C19 (16%) and CYP2D6 (1%).


    Excretion

    Following a single radiolabeled dose of 100 mg encorafenib, 47% (5% unchanged) of the administered dose was recovered in feces and 47% (2% unchanged) in urine.


    Specific Populations

    No clinically significant differences in the pharmacokinetics of encorafenib were observed based on age (19 to 94 years), sex, body weight (34 to 168 kg), mild hepatic impairment (Child-Pugh Class A), and mild or moderate renal impairment (CLcr 30 to <90 mL/min). The effect of race or ethnicity, moderate or severe hepatic impairment (Child-Pugh Class B or C), and severe renal impairment (CLcr <30 mL/min) on encorafenib pharmacokinetics have not been studied.


    Drug Interaction Studies


    Clinical Studies


    In Vitro Studies

    13 Nonclinical Toxicology


    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility


    Carcinogenicity studies with encorafenib have not been conducted. Encorafenib was not genotoxic in studies evaluating reverse mutations in bacteria, chromosomal aberrations in mammalian cells, or micronuclei in bone marrow of rats.

    No dedicated fertility studies were performed with encorafenib in animals. In a general toxicology study in rats, decreased testes and epididymis weights, tubular degeneration in testes, and oligospermia in epididymides were observed at doses approximately 13 times the human exposure at the 450 mg clinical dose based on AUC. No effects on reproductive organs were observed in either sex in any of the non-human primate toxicity studies.

    13.2 Animal Toxicology and/or Pharmacology


    Adverse histopathology findings of hyperplasia and hyperkeratosis occurred in the stomach of rats at encorafenib doses of 20 mg/kg/day (approximately 14 times the human exposure at the 450 mg clinical dose based on AUC) or greater, in both 4 and 13-week studies.

    14 Clinical Studies


    14.1 BRAF V600E or V600K Mutation-Positive Unresectable or Metastatic Melanoma


    BRAFTOVI in combination with binimetinib was evaluated in a randomized, active-controlled, open-label, multicenter trial (COLUMBUS; NCT01909453). Eligible patients were required to have BRAF V600E or V600K mutation-positive unresectable or metastatic melanoma, as detected using the bioMerieux THxID™BRAF assay. Patients were permitted to have received immunotherapy in the adjuvant setting and one prior line of immunotherapy for unresectable locally advanced or metastatic disease. Prior use of BRAF inhibitors or MEK inhibitors was prohibited. Randomization was stratified by American Joint Committee on Cancer (AJCC) Stage (IIIB, IIIC, IVM1a or IVM1b, versus IVM1c), Eastern Cooperative Oncology Group (ECOG) performance status (0 versus 1), and prior immunotherapy for unresectable or metastatic disease (yes versus no).

    Patients were randomized (1:1:1) to receive BRAFTOVI 450 mg once daily in combination with binimetinib 45 mg twice daily (BRAFTOVI in combination with binimetinib), BRAFTOVI 300 mg once daily, or vemurafenib 960 mg twice daily. Treatment continued until disease progression or unacceptable toxicity. Only the results of the approved dosing (BRAFTOVI 450 mg in combination with binimetinib 45 mg) are described below.

    The major efficacy outcome measure was progression-free survival (PFS), as assessed by a blinded independent central review, to compare BRAFTOVI in combination with binimetinib with vemurafenib. Additional efficacy outcome measures included overall survival (OS), as well as objective response rate (ORR) and duration of response (DoR) which were assessed by central review.

    A total of 577 patients were randomized, 192 to the BRAFTOVI in combination with binimetinib arm, 194 to the BRAFTOVI arm, and 191 to the vemurafenib arm. Of the 383 patients randomized to either the BRAFTOVI in combination with binimetinib or the vemurafenib arms, the median age was 56 years (20 to 89 years), 59% were male, 91% were White, and 72% had baseline ECOG performance status of 0. Ninety-five percent (95%) had metastatic disease, 65% were Stage IVM1c, and 4% received prior CTLA-4, PD-1, or PD-L1 directed antibodies. Twenty-eight percent (28%) had elevated baseline serum lactate dehydrogenase (LDH), 45% had ≥3 organs with tumor involvement at baseline, and 3% had brain metastases. Based on centralized testing, 100% of patients' tumors tested positive for BRAF mutations; BRAF V600E (88%), BRAF V600K (11%), or both (<1%).

    BRAFTOVI in combination with binimetinib demonstrated a statistically significant improvement in PFS compared to vemurafenib. Efficacy results are summarized in Table 11 and Figure 1.
    Table 11: Efficacy Results for COLUMBUS
    BRAFTOVI with binimetinib N=192 Vemurafenib N=191
    CI = Confidence interval; CR = Complete response; DoR = Duration of response; HR = Hazard ratio; NE = Not estimable; ORR = Overall response rate; OS = Overall survival; PFS = Progression-free survival; PR = Partial response.

    Progression-Free Survival

      Number of events (%)
    98 (51)
    106 (55)

        Progressive disease
    88 (46)
    104 (54)

        Death
    10 (5)
    2 (1)

      Median PFS, months (95% CI)
    14.9 (11, 18.5)
    7.3 (5.6, 8.2)

      HR (95% CI)Estimated with Cox proportional hazard model adjusted by the following stratification factors: American Joint Committee on Cancer (AJCC) Stage (IIIB, IIIC, IVM1a or IVM1b, versus IVM1c) and Eastern Cooperative Oncology Group (ECOG) performance status (0 versus 1).

    0.54 (0.41, 0.71)

      P-valueLog-rank test adjusted by the same stratification factors.

    <0.0001

    Overall Survival Based on a cutoff date of 17.6 months after the date of the PFS analysis.

      Number of events (%)
    105 (55)
    127 (67)

      Median OS, months (95% CI)
    33.6 (24.4, 39.2)
    16.9 (14.0, 24.5)

      HR (95% CI)

    0.61 (0.47, 0.79)

    Overall Response Rate

      ORR (95% CI)
    63% (56%, 70%)
    40% (33%, 48%)

        CR
    8%
    6%

        PR
    55%
    35%

    Duration of Response

      Median DoR, months (95% CI)
    16.6 (12.2, 20.4)
    12.3 (6.9, 16.9)

    Figure 1: Kaplan-Meier Curves for Progression-Free Survival in COLUMBUS

    14.2 BRAF V600E Mutation-Positive Metastatic Colorectal Cancer (CRC)


    BRAFTOVI in combination with cetuximab was evaluated in a randomized, active-controlled, open-label, multicenter trial (BEACON CRC; NCT02928224). Eligible patients were required to have BRAF V600E mutation-positive metastatic colorectal cancer (CRC), as detected using the Qiagen therascreen BRAF V600E RGQ polymerase chain reaction (PCR) Kit, with disease progression after 1 or 2 prior regimens. Other key eligibility criteria included absence of prior treatment with a RAF, MEK, or EGFR inhibitor, eligibility to receive cetuximab per local labeling with respect to tumor RAS status, and ECOG performance status (PS) 0–1. Randomization was stratified by Eastern Cooperative Oncology Group (ECOG) performance status (0 versus 1), prior use of irinotecan (yes versus no), and cetuximab product used (US-licensed versus EU-approved).

    Patients were randomized 1:1:1 to one of the following treatment arms:
    • •BRAFTOVI 300 mg orally once daily in combination with cetuximab (BRAFTOVI/cetuximab arm)
    • •BRAFTOVI 300 mg orally once daily in combination with binimetinib and cetuximab
    • •Irinotecan with cetuximab or FOLFIRI with cetuximab (control arm)

    The dosage of cetuximab in all patients was 400 mg/m2 intravenously for the first dose followed by 250 mg/m2 weekly.

    Patients in the control arm received cetuximab with either irinotecan 180 mg/m2 intravenously on Days 1 and 15 of each 28-day cycle or FOLFIRI intravenously (irinotecan 180 mg/m2 on Days 1 and 15; folinic acid 400 mg/m2 on Days 1 and 15; then fluorouracil 400 mg/m2 bolus on Days 1 and 15 followed by fluorouracil 2400 mg/m2/day by continuous infusion over 2 days).

    Treatment continued until disease progression or unacceptable toxicity. Only the results of the approved regimen (BRAFTOVI in combination with cetuximab) are described below.

    The major efficacy outcome measure was overall survival (OS). Additional efficacy outcome measures included progression-free survival (PFS), overall response rate (ORR), and duration of response (DoR) as assessed by blinded independent central review (BICR). OS and PFS were assessed in all randomized patients. ORR and DoR were assessed in the subset of the first 220 patients included in the randomized portion of the BRAFTOVI/cetuximab and control arm of the study.

    A total of 220 patients were randomized to the BRAFTOVI/cetuximab arm and 221 to the control arm. Of these 441 patients, the median age was 61 years; 53% were female; 80% were White and 15% were Asian. Fifty percent (50%) had baseline ECOG performance status of 0; 66% received 1 prior therapy and 34% received 2; 93% received prior oxaliplatin and 52% received prior irinotecan.

    BRAFTOVI in combination with cetuximab demonstrated a statistically significant improvement in OS, ORR, and PFS compared to the active comparator. Efficacy results are summarized in Table 12 and Figure 2.
    Table 12: Efficacy Results From BEACON CRC
    BRAFTOVI with cetuximab N = 220 Irinotecan with cetuximab or FOLFIRI with cetuximab N = 221
    CI = Confidence interval; CR = Complete response; DoR = Duration of response; HR = Hazard ratio; NR = Not reached; ORR = Overall response rate; OS = Overall survival; PFS = Progression-free survival; PR = Partial response.

    Overall Survival

      Number of Events (%)
    93 (42)
    114 (52)

      Median OS, months (95% CI)
    8.4 (7.5, 11.0)
    5.4 (4.8, 6.6)

      HR (95% CI)Stratified by ECOG PS, source of cetuximab (US-licensed versus EU-approved) and prior irinotecan use at randomization. , Stratified Cox proportional hazard model.

    0.60 (0.45, 0.79)

      P-value , Stratified log-rank test, tested at alpha level of 0.0084.

    0.0003

    Overall Response Rate (per BICR)

      ORR (95% CI)BRAFTOVI/cetuximab arm (n=113) and control arm (n=107).

    20% (13%, 29%)
    2% (0%, 7%)

        CR
    5%
    0%

        PR
    15%
    2%

      P-value , Cochran-Mantel-Haenszel test; tested at alpha level of 0.05.

    <0.0001

      Median DoR, months (95% CI)
    6.1 (4.1, 8.3)
    NR (2.6, NR)

    Progression Free Survival (per BICR)

      Number of events (%)
    133 (60)
    128 (58)

        Progressive disease
    110 (50)
    101 (46)

        Death
    23 (10)
    27 (12)

      Median PFS, months (95% CI)
    4.2 (3.7, 5.4)
    1.5 (1.4, 1.7)

      HR (95% CI) ,

    0.40 (0.31, 0.52)

      P-value , Stratified log-rank test, tested at alpha level of 0.0234.

    < 0.0001

    Figure 2: Kaplan-Meier Curves for Overall Survival in BEACON CRC

    14.3 BRAF V600E Mutation-Positive Metastatic Non-Small Cell Lung Cancer


    BRAFTOVI in combination with binimetinib was evaluated in an open-label, multicenter, single-arm study in patients with BRAF V600E mutation-positive metastatic non-small cell lung cancer (NSCLC) (PHAROS; NCT03915951). Eligible patients had a diagnosis of histologically-confirmed metastatic NSCLC with BRAF V600E mutation that was treatment-naĂŻve or had been previously treated with 1 prior line of systemic therapy in the metastatic setting (platinum-based chemotherapy and/or anti-PD-1/PD-L1 therapies), age 18 years or older, Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 or 1, and measurable disease as defined by Response Evaluation Criteria in Solid Tumors (RECIST) v1.1. Prior use of BRAF inhibitors or MEK inhibitors was not allowed.

    Patients received BRAFTOVI 450 mg once daily and binimetinib 45 mg orally twice daily until disease progression or unacceptable toxicity. The major efficacy outcome measures were objective response rate (ORR) per RECIST v1.1 and duration of response (DoR) as assessed by independent review committee (IRC).

    In the efficacy population, BRAF V600E mutation status was determined by prospective local testing using tumor tissue (78%) or blood (22%) specimens. Of the 98 patients with BRAF V600E mutation, 6 patients were enrolled into the trial based on testing of their tumor tissue specimens with the FoundationOne CDx tissue test. Of the remaining 92 patients enrolled based on local testing, 68 patients had their tumor tissue specimens retrospectively confirmed as having BRAF V600E positive status by the FoundationOne CDx tissue test. The remaining patients had either BRAF V600E negative status (n=5) or had unevaluable results (n=19) by the FoundationOne CDx tissue test. In addition, plasma samples from 81 out of 98 patients were retrospectively tested using the FoundationOne Liquid CDx assay. Of the 81 patients, 48 were confirmed positive for BRAF V600E, while 33 patients were BRAF V600E mutation negative by FoundationOne Liquid CDx assay. The remaining 17 samples had unevaluable results with FoundationOne Liquid CDx assay.

    The efficacy population included 59 treatment-naĂŻve patients and 39 previously-treated patients. Among these 98 patients, the median age was 70 years (range: 47 to 86); 53% female; 88% White, 7% Asian, 3% Black or African American, and 1% American Indian or Alaska Native; 99% were not Hispanic or Latino; 13% were current smokers and 57% were former smokers; 73% had ECOG PS of 1; and 97% had adenocarcinoma. All patients had metastatic disease, and 8% had brain metastases at baseline.

    Efficacy results for patients with BRAF V600E mutation-positive metastatic NSCLC are summarized in Table 13.
    Table 13: Efficacy Results for PHAROS
    CI = Confidence interval; CR = Complete response; DoR = Duration of response; N = Number of patients; NE = Not estimable; ORR = Objective response rate; PR = Partial response.

    BRAFTOVI with binimetinib

    Efficacy Parameter

    Treatment naĂŻve

    (N=59)

    Previously treated

    (N=39)

    Objective Response Rate Assessed by Independent Central Review (ICR).

        ORR (95% CI)
    75% (62, 85)
    46% (30, 63)

        CR
    15%
    10%

        PR
    59%
    36%

    Duration of Response

    N=44
    N=18

        Median DoR, months (95% CI)
    NE (23.1, NE)
    16.7 (7.4, NE)

        % with DoR ≥6 months
    75%
    67%

        % with DoR ≥12 months
    59%
    33%

    16 How Supplied/storage And Handling


    BRAFTOVI (encorafenib) is supplied as 75 mg hard gelatin capsules.

    75 mg: stylized "A" on beige cap and "LGX 75mg" on white body, available in cartons (NDC 70255-025-01) containing two bottles of 90 capsules each (NDC 70255-025-02) and cartons (NDC 70255-025-03) containing two bottles of 60 capsules each (NDC 70255-025-04).

    STORAGE AND HANDLING SECTION


    Store at 20°C to 25°C (68°F to 77°F); excursions permitted between 15°C and 30°C (59°F and 86°F) [see USP Controlled Room Temperature]. Do not use if safety seal under cap is broken or missing. Dispense in original bottle. Do not remove desiccant. Protect from moisture. Keep container tightly closed.

    17 Patient Counseling Information


    Advise the patient to read the FDA-approved patient labeling (Medication Guide).

    Inform patients of the following:


    New Primary Malignancies

    Advise patients that BRAFTOVI increases the risk of developing new primary cutaneous and non-cutaneous malignancies. Advise patients to contact their healthcare provider immediately for change in or development of new skin lesions [see Warnings and Precautions (5.1)].

    Tumor Promotion in BRAF Wild-Type Tumors

    Advise patients of the need to confirm BRAF V600E or V600K mutation prior to initiating BRAFTOVI [see Warnings and Precautions (5.2)].

    Cardiomyopathy

    Advise patients to report any symptoms of heart failure to their healthcare provider [see Warnings and Precautions (5.3)].

    Hepatotoxicity

    Advise patients that serial testing of serum liver tests (ALT, AST, bilirubin) is recommended during treatment with BRAFTOVI. Instruct patients to report symptoms of liver dysfunction including jaundice, dark urine, nausea, vomiting, loss of appetite, fatigue, bruising, or bleeding [see Warnings and Precautions (5.4)].


    Hemorrhage

    Advise patients to notify their healthcare provider immediately with any symptoms suggestive of hemorrhage, such as unusual bleeding [see Warnings and Precautions (5.5) ].


    Uveitis

    Advise patients to contact their healthcare provider if they experience any changes in their vision [see Warnings and Precautions (5.6) ].


    QT Prolongation

    Advise patients that BRAFTOVI can cause QTc interval prolongation and to inform their physician if they have any QTc interval prolongation symptoms, such as syncope [see Warnings and Precautions (5.7) ].


    Embryo-Fetal Toxicity
    • •Advise females with reproductive potential of the potential risk to a fetus. Advise females to contact their healthcare provider if they become pregnant, or if pregnancy is suspected, during treatment with BRAFTOVI [see Warnings and Precautions (5.8) , Use in Specific Populations (8.1)].
    • •Advise females of reproductive potential to use effective non-hormonal contraception during treatment with BRAFTOVI and for 2 weeks after the last dose [Use in Specific Populations (8.3)].


    Lactation

    Advise women not to breastfeed during treatment with BRAFTOVI and for 2 weeks after the last dose [see Use in Specific Populations (8.2)].


    Infertility

    Advise males of reproductive potential that BRAFTOVI may impair fertility [see Use in Specific Populations (8.3)].


    Strong or Moderate CYP3A Inducers or Inhibitors

    Coadministration of BRAFTOVI with a strong or moderate CYP3A inhibitor may increase encorafenib concentrations; coadministration of BRAFTOVI with a strong or moderate CYP3A inducer may decrease encorafenib concentrations. Advise patients that they may need to avoid certain medications while taking BRAFTOVI and to inform their healthcare provider of all concomitant medications, including prescription medicines, over-the-counter drugs, vitamins, and herbal products. Advise patients to avoid grapefruit and grapefruit juice while taking BRAFTOVI [see Drug Interactions (7.1)].


    Storage

    BRAFTOVI is moisture sensitive. Advise patients to store BRAFTOVI in the original bottle with desiccant and to keep the cap of the bottle tightly closed. Do not remove the desiccants from the bottle.


    This product's labeling may have been updated. For the most recent prescribing information, please visit www.pfizer.com.

    Distributed by:

    Array BioPharma Inc., a wholly owned subsidiary of Pfizer Inc.3200 Walnut StreetBoulder, CO 80301

    © 2023 Array BioPharma Inc. All rights reserved.BRAFTOVI® is a registered trademark of Array BioPharma Inc. in the United States and various other countries.

    LAB-1428-3.0

    Spl Medguide Section

    Risk of new skin cancers. BRAFTOVI when used alone, or with binimetinib or cetuximab, may cause skin cancers called cutaneous squamous cell carcinoma or basal cell carcinoma.Talk to your healthcare provider about your risk for these cancers.Check your skin and tell your healthcare provider right away about any skin changes, including a:new wart
    • skin sore or reddish bump that bleeds or does not heal
    • change in size or color of a moleYour healthcare provider should check your skin before treatment with BRAFTOVI, every 2 months during treatment, and for up to 6 months after you stop treatment with BRAFTOVI to look for any new skin cancers.
    • Your healthcare provider should also check for cancers that may not occur on the skin. Tell your healthcare provider about any new symptoms that develop during treatment with BRAFTOVI.
    • See " What are the possible side effects of BRAFTOVI?" for more information about side effects.in combination with a medicine called binimetinib to treat people with a type of skin cancer called melanoma:
    that has spread to other parts of the body or cannot be removed by surgery, and
    • that has a certain type of abnormal "BRAF" gene
    • in combination with a medicine called cetuximab, for the treatment of adults with cancer of your colon or rectum (colorectal cancer):
    that has been previously treated, and
    • that has spread to other parts of the body, and
    • that has a certain type of abnormal "BRAF" gene
    • in combination with a medicine called binimetinib to treat adults with a type of lung cancer called non-small cell lung cancer (NSCLC):
    that has spread to other parts of the body, and
    • that has a certain type of abnormal “BRAF” gene
    BRAFTOVI should not be used to treat people with wild-type BRAF melanoma, wild-type BRAF colorectal cancer, or wild-type BRAF NSCLC. Your healthcare provider will perform a test to make sure that BRAFTOVI is right for you.It is not known if BRAFTOVI is safe and effective in children.
    have had bleeding problems
    • have eye problems
    • have heart problems, including a condition called long QT syndrome
    • have been told that you have low blood levels of potassium, calcium, or magnesium
    • have liver or kidney problems
    • are pregnant or plan to become pregnant. BRAFTOVI can harm your unborn baby.
    Females who are able to become pregnant should use effective non-hormonal birth control (contraception) during treatment with BRAFTOVI and for 2 weeks after the last dose of BRAFTOVI. Birth control methods that contain hormones (such as birth control pills, injections or transdermal systems) may not work as well during treatment with BRAFTOVI.
    • Talk to your healthcare provider about birth control methods that may be right for you during this time.
    • Your healthcare provider will do a pregnancy test before you start taking BRAFTOVI. Tell your healthcare provider right away if you become pregnant or think you might be pregnant during treatment with BRAFTOVI.
    • are breastfeeding or plan to breastfeed. It is not known if BRAFTOVI passes into your breast milk. Do not breastfeed during treatment with BRAFTOVI and for 2 weeks after the last dose of BRAFTOVI. Talk to your healthcare provider about the best way to feed your baby during this time.
    Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. BRAFTOVI and certain other medicines can affect each other, causing side effects or affecting how BRAFTOVI or the other medicines work. Know the medicines you take. Keep a ul of them to show your healthcare provider and pharmacist when you get a new medicine.
    Take BRAFTOVI exactly as your healthcare provider tells you. Do not change your dose or stop taking BRAFTOVI unless your healthcare provider tells you to.
    • For melanoma and NSCLC, BRAFTOVI is given in combination with binimetinib. Take BRAFTOVI by mouth one time each day.
    • For colorectal cancer, take BRAFTOVI by mouth one time each day. You will also receive cetuximab through a vein in your arm (intravenously) given by your healthcare provider.
    • BRAFTOVI may be taken with or without food.
    • Avoid grapefruit during treatment with BRAFTOVI. Grapefruit products may increase the amount of BRAFTOVI in your body.
    • If you miss a dose of BRAFTOVI, take it as soon as you remember. If it is within 12 hours of your next scheduled dose, take your next dose at your regular time. Do not make up for the missed dose.
    • Do not take an extra dose if you vomit after taking your scheduled dose. Take your next dose at your regular time.
    • If you stop treatment with binimetinib or cetuximab, talk to your healthcare provider about your BRAFTOVI treatment. Your BRAFTOVI dose may need to be changed or stopped. Heart problems, including heart failure. BRAFTOVI, when taken with binimetinib, can cause heart problems. Your healthcare provider will check your heart function before and during treatment with BRAFTOVI. Tell your healthcare provider right away if you get any of the following signs and symptoms of a heart problem:
    feeling like your heart is pounding or racing
    • shortness of breath
    • swelling in your hands, ankles legs or feet
    • feeling faint or lightheaded
    • Liver problems. BRAFTOVI, when taken with binimetinib, can cause liver problems. Your healthcare provider will perform blood tests to check your liver function before and during treatment with BRAFTOVI. Tell your healthcare provider if you get any of the following signs and symptoms of a liver problem:yellowing of your skin or your eyes
    • dark or brown (tea-colored) urine
    • nausea or vomiting
    • loss of appetitetiredness
    • bruising
    • bleedingBleeding problems. BRAFTOVI, when taken with binimetinib or cetuximab, can cause serious bleeding problems, including in your stomach or brain, that can lead to death. Tell your healthcare provider and get medical help right away if you develop any signs of bleeding, including:
    headaches, dizziness, or feeling weak
    • cough up blood or blood clots
    • vomit blood or your vomit looks like “coffee grounds”
    • red or black stools that look like tar
    • Eye problems. BRAFTOVI, when taken with binimetinib, can cause eye problems. Your healthcare provider should perform an eye exam regularly. Tell your healthcare provider right away if you develop any new or worsening symptoms of eye problems, including:
    blurred vision, loss of vision, or other vision changes
    • see colored dots
    • see halos (blurred outline around objects)
    • eye pain, swelling, or redness
    • Changes in the electrical activity of your heart called QT prolongation. QT prolongation can cause irregular heartbeats that can be life threatening. Your healthcare provider should do tests before you start taking BRAFTOVI with binimetinib or cetuximab and during your treatment to check your body salts (electrolytes). Tell your healthcare provider right away if you feel faint, lightheaded, dizzy or if you feel your heart beating irregularly or fast during treatment with BRAFTOVI and binimetinib or cetuximab. These symptoms may be related to QT prolongation.
    Your healthcare provider may change your dose, temporarily stop, or permanently stop treatment with BRAFTOVI if you have certain side effects.

    The most common side effects of BRAFTOVI when taken in combination with binimetinib for melanoma include:
    fatigue
    • nausea
    • vomiting
    • abdominal pain
    • pain or swelling of your joints (arthralgia)
    The most common side effects of BRAFTOVI when taken in combination with cetuximab for colorectal cancer include:
    fatigue
    • nausea
    • diarrhea
    • acne-like rash (dermatitis acneiform)stomach-area (abdominal) pain
    • decreased appetite
    • pain or swelling of your joints (arthralgia)
    • rashfatigue
    • nausea
    • diarrhea
    • muscle or joint pain
    • vomiting
    • stomach-area (abdominal) painblurred vision, loss of vision, or other vision changes
    • constipation
    • shortness of breath
    • rash
    • coughStore BRAFTOVI at room temperature between 68°F to 77°F (20°C to 25°C).
    • Store BRAFTOVI in the original bottle.
    • Keep the BRAFTOVI bottle tightly closed and protect it from moisture.
    • BRAFTOVI comes with a desiccant packet in the bottle to help protect your medicine from moisture. Do not remove the desiccant packet from the bottle.
    Keep BRAFTOVI and all medicines out of the reach of children.

    This Medication Guide has been approved by the U.S. Food and Drug Administration.
    Revised: 10/2023                      

    MEDICATION GUIDE BRAFTOVI® (braf-TOE-vee)(encorafenib)capsules

    Important information: BRAFTOVI is used with other medicines, either binimetinib or cetuximab. Read the Medication Guide that comes with binimetinib if used with binimetinib and talk to your healthcare provider about cetuximab if used with cetuximab.
    What is the most important information I should know about BRAFTOVI? BRAFTOVI may cause serious side effects, including:
    •
    o o o
         

    What is BRAFTOVI? BRAFTOVI is a prescription medicine used:
    •o o •o o o •o o

    Before taking BRAFTOVI, tell your healthcare provider about all of your medical conditions, including if you:
    • • • • • •o o o •

    How should I take BRAFTOVI?
    • • • • • • • •
    What are the possible side effects of BRAFTOVI? BRAFTOVI may cause serious side effects, including: See " What is the most important information I should know about BRAFTOVI? "
    • o o o o •
    o o o o
    o o o
    • o o o o • o o o o • • • • • •
    • • • •
    • • • •

    The most common side effects of BRAFTOVI when taken in combination with binimetinib for NSCLC include:
    • • • • • •
    • • • • •

    BRAFTOVI may cause fertility problems in males. Talk to your healthcare provider if this is a concern for you.

    These are not all of the possible side effects of BRAFTOVI.

    Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

    You may also report side effects to Pfizer Inc. at 1-800-438-1985.

    How should I store BRAFTOVI?
    • • • •

    General information about the safe and effective use of BRAFTOVI. Medicines are sometimes prescribed for purposes other than those uled in a Medication Guide. Do not use BRAFTOVI for a condition for which it was not prescribed. Do not give BRAFTOVI to other people, even if they have the same symptoms that you have. It may harm them. You can ask your healthcare provider or pharmacist for information about BRAFTOVI that is written for health professionals.

    What are the ingredients in BRAFTOVI? Active ingredient: encorafenib Inactive ingredients: copovidone, poloxamer 188, microcrystalline cellulose, succinic acid, crospovidone, colloidal silicon dioxide, and magnesium stearate of vegetable origin Capsule shell: gelatin, titanium dioxide, iron oxide red, iron oxide yellow, ferrosoferric oxide, monogramming ink (pharmaceutical glaze, ferrosoferric oxide, propylene glycol)Distributed by: Array BioPharma Inc., a wholly owned subsidiary of Pfizer Inc. Boulder, Colorado 80301.BRAFTOVI® is a registered trademark of Array BioPharma Inc. in the United States and various other countries.LAB-1429-3.0For more information, go to www.BRAFTOVIMEKTOVI.com or call 1-844-792-7729.© 2022 Array BioPharma Inc. All rights reserved.

    Principal Display Panel - 75 Mg Capsule Bottle Label - 025-02


    DISPENSE THE ENCLOSED MEDICATION GUIDE TO EACH PATIENT

    NDC 70255-025-02

    BRAFTOVI® (encorafenib) capsules

    75 mg

    Rx only90 Capsules

    Principal Display Panel - 75 Mg Capsule Bottle Carton


    DISPENSE THE ENCLOSED MEDICATION GUIDE TO EACH PATIENT

    NDC 70255-025-01

    BRAFTOVI® (encorafenib) capsules

    75 mg

    Rx only2 Bottles x 90 Capsules

    Principal Display Panel - 75 Mg Capsule Bottle Label - 025-06


    DISPENSE THE ENCLOSED MEDICATION GUIDE TO EACH PATIENT

    NDC 70255-025-06

    BRAFTOVI® (encorafenib) capsules

    75 mg

    Rx only60 Capsules

    Sample–Not For Sale

    Principal Display Panel - 75 Mg Capsule Bottle Label - 025-05


    DISPENSE THE ENCLOSED MEDICATION GUIDE TO EACH PATIENT

    NDC 70255-025-05

    BRAFTOVI® (encorafenib) capsules

    75 mg

    Rx only90 Capsules

    Sample–Not For Sale

    DISCLAIMER:

    "This tool does not provide medical advice, and is for informational and educational purposes only, and is not a substitute for professional medical advice, treatment or diagnosis. Call your doctor to receive medical advice. If you think you may have a medical emergency, please dial 911."

    "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service."

    "This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product."

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