UNITUXIN (DINUTUXIMAB) INJECTION [UNITED THERAPEUTICS CORP.]

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UNITUXIN (DINUTUXIMAB) INJECTION [UNITED THERAPEUTICS CORP.]
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NDC 66302-014-01
Set ID d66bdf0d-9d65-45de-ae5b-a58617c27492
Category HUMAN PRESCRIPTION DRUG LABEL
Packager United Therapeutics Corporation
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Application Number BLA125516
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  • HIGHLIGHTS OF PRESCRIBING INFORMATION
    These highlights do not include all the information needed to use UNITUXIN safely and effectively. See Full Prescribing Information for UNITUXIN.

    UNITUXIN® (dinutuximab) injection, for intravenous use
    Initial U.S. Approval: 2015

    WARNING: SERIOUS INFUSION REACTIONS AND NEUROTOXICITY

    See full prescribing information for complete boxed warning.

    • Infusion Reactions: Life-threatening infusion adverse reactions occur with Unituxin. Administer required prehydration and premedication. Immediately interrupt for severe infusion reactions and permanently discontinue for anaphylaxis [see Dosage and Administration (2.2, 2.3) and Warnings and Precautions (5.1)].
    • Neurotoxicity: Unituxin causes severe neuropathic pain. Administer intravenous opioid prior to, during, and for 2 hours following completion of the Unituxin infusion. Severe peripheral sensory neuropathy ranged from 2% to 9% in patients with neuroblastoma. Severe peripheral motor neuropathy has also been reported. Discontinue for severe unresponsive pain, severe sensory neuropathy, and moderate to severe peripheral motor neuropathy [see Dosage and Administration (2.2, 2.3) and Warnings and Precautions (5.2)].

    INDICATIONS AND USAGE

    Unituxin is a GD2-binding monoclonal antibody indicated, in combination with granulocyte-macrophage colony-stimulating factor (GM-CSF), interleukin-2 (IL-2), and 13-cis-retinoic acid (RA), for the treatment of pediatric patients with high-risk neuroblastoma who achieve at least a partial response to prior first-line multiagent, multimodality therapy. (1)

    DOSAGE AND ADMINISTRATION

    • 17.5 mg/m2/day as a diluted intravenous infusion over 10 to 20 hours for 4 consecutive days for up to 5 cycles. (2.1, 2.4)

    DOSAGE FORMS AND STRENGTHS

    • Injection: 17.5 mg/5 mL (3.5 mg/mL) in a single-dose vial. (3)

    CONTRAINDICATIONS

    • History of anaphylaxis to dinutuximab. (4)

    WARNINGS AND PRECAUTIONS

    • Neurological Disorders of the Eye: Interrupt Unituxin for dilated pupil with sluggish light reflex or other visual disturbances and permanently discontinue Unituxin for recurrent eye disorders or loss of vision. (5.2)
    • Prolonged Urinary Retention and Transverse Myelitis: Permanently discontinue Unituxin and institute supportive care. (5.2)
    • Reversible Posterior Leukoencephalopathy Syndrome (RPLS): Permanently discontinue Unituxin and institute supportive care for signs and symptoms of RPLS. (5.2)
    • Capillary Leak Syndrome and Hypotension: Administer required prehydration and monitor patients closely during treatment. Depending upon severity, manage by interruption, infusion rate reduction, or permanent discontinuation. (5.3, 5.4)
    • Infection: Interrupt until resolution of systemic infection. (5.5)
    • Bone Marrow Suppression: Monitor peripheral blood counts during Unituxin therapy. (5.6)
    • Electrolyte Abnormalities: Monitor serum electrolytes closely. (5.7)
    • Atypical Hemolytic Uremic Syndrome: Permanently discontinue Unituxin and institute supportive management. (5.8)
    • Embryo-Fetal Toxicity: May cause fetal harm. Advise females of reproductive potential of potential risk to a fetus and to use effective contraception. (5.9, 8.1, 8.3)

    ADVERSE REACTIONS

    The most common adverse drug reactions (≥25%) are pain, pyrexia, thrombocytopenia, lymphopenia, infusion reactions, hypotension, hyponatremia, increased alanine aminotransferase, anemia, vomiting, diarrhea, hypokalemia, capillary leak syndrome, neutropenia, urticaria, hypoalbuminemia, increased aspartate aminotransferase, and hypocalcemia. (5, 6.1)

    The most common serious adverse reactions (≥5%) are infections, infusion reactions, hypokalemia, hypotension, pain, fever, and capillary leak syndrome. (5, 6.1)


    To report SUSPECTED ADVERSE REACTIONS, contact United Therapeutics Corp. at 1-866-458-6479 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

    See 17 for PATIENT COUNSELING INFORMATION.

    Revised: 9/2020

  • Table of Contents

    FULL PRESCRIBING INFORMATION: CONTENTS*

    WARNING: SERIOUS INFUSION REACTIONS AND NEUROTOXICITY

    1 INDICATIONS AND USAGE

    2 DOSAGE AND ADMINISTRATION

    2.1 Recommended Dose

    2.2 Required Pre-treatment Guidelines

    2.3 Dosage Modifications

    2.4 Instructions for Preparation and Administration

    3 DOSAGE FORMS AND STRENGTHS

    4 CONTRAINDICATIONS

    5 WARNINGS AND PRECAUTIONS

    5.1 Serious Infusion Reactions

    5.2 Neurotoxicity

    5.3 Capillary Leak Syndrome

    5.4 Hypotension

    5.5 Infection

    5.6 Bone Marrow Suppression

    5.7 Electrolyte Abnormalities

    5.8 Atypical Hemolytic Uremic Syndrome

    5.9 Embryo-Fetal Toxicity

    6 ADVERSE REACTIONS

    6.1 Clinical Trials Experience

    6.2 Immunogenicity

    6.3 Postmarketing Experience

    7 DRUG INTERACTIONS

    8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    8.2 Lactation

    8.3 Females and Males of Reproductive Potential

    8.4 Pediatric Use

    8.5 Geriatric Use

    8.6 Renal Impairment

    8.7 Hepatic Impairment

    11 DESCRIPTION

    12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    12.3 Pharmacokinetics

    13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    13.2 Animal Toxicology and/or Pharmacology

    14 CLINICAL STUDIES

    16 HOW SUPPLIED/STORAGE AND HANDLING

    17 PATIENT COUNSELING INFORMATION

    *
    Sections or subsections omitted from the full prescribing information are not listed.
  • BOXED WARNING (What is this?)

    WARNING: SERIOUS INFUSION REACTIONS AND NEUROTOXICITY

    Infusion Reactions

    • Serious and potentially life-threatening infusion reactions occurred in 26% of patients treated with Unituxin. Administer required prehydration and premedication including antihistamines prior to each Unituxin infusion. Monitor patients closely for signs and symptoms of an infusion reaction during and for at least four hours following completion of each Unituxin infusion. Immediately interrupt Unituxin for severe infusion reactions and permanently discontinue Unituxin for anaphylaxis (2.2, 2.3, 5.1).

    Neurotoxicity

    • Unituxin causes serious neurologic adverse reactions including severe neuropathic pain and peripheral neuropathy.

      Severe neuropathic pain occurs in the majority of patients. Administer intravenous opioid prior to, during, and for 2 hours following completion of the Unituxin infusion.

      In clinical studies of patients with high-risk neuroblastoma, Grade 3 peripheral sensory neuropathy occurred in 2% to 9% of patients. In clinical studies of Unituxin and related GD2-binding antibodies, severe motor neuropathy has occurred. Resolution of motor neuropathy did not occur in all cases. Discontinue Unituxin for severe unresponsive pain, severe sensory neuropathy, and moderate to severe peripheral motor neuropathy (2.2, 2.3, 5.2).

  • 1 INDICATIONS AND USAGE

    Unituxin (dinutuximab) is indicated, in combination with granulocyte-macrophage colony-stimulating factor (GM-CSF), interleukin-2 (IL-2), and 13-cis-retinoic acid (RA), for the treatment of pediatric patients with high-risk neuroblastoma who achieve at least a partial response to prior first-line multiagent, multimodality therapy [see Clinical Studies (14)].

  • 2 DOSAGE AND ADMINISTRATION

    • Verify that patients have adequate hematologic, respiratory, hepatic, and renal function prior to initiating each course of Unituxin [see Clinical Studies (14)].
    • Administer required premedication and hydration prior to initiation of each Unituxin infusion [see Dosage and Administration (2.2)].

    2.1 Recommended Dose

    • The recommended dose of Unituxin is 17.5 mg/m2/day administered as an intravenous infusion over 10 to 20 hours for 4 consecutive days for a maximum of 5 cycles (Table 1 and Table 2) [see Dosage and Administration (2.4) and Clinical Studies (14)].
    • Initiate at an infusion rate of 0.875 mg/m2/hour for 30 minutes. The infusion rate can be gradually increased as tolerated to a maximum rate of 1.75 mg/m2/hour. Follow dose modification instructions for adverse reactions [see Dosage and Administration (2.3)].
    Table 1: Schedule of Unituxin Administration for Cycles 1, 3, and 5
    Cycle Day1 through 345678 through 24*
    *
    Cycles 1, 3, and 5 are 24 days in duration.
    UnituxinXXXX
    Table 2: Schedule of Unituxin Administration for Cycles 2 and 4
    Cycle Day1 through 789101112 through 32*
    *
    Cycles 2 and 4 are 32 days in duration.
    UnituxinXXXX

    2.2 Required Pre-treatment Guidelines

    Intravenous Hydration

    • Administer 0.9% Sodium Chloride Injection, USP 10 mL/kg as an intravenous infusion over 1 hour just prior to initiating each Unituxin infusion.

    Analgesics

    • Administer morphine sulfate (50 mcg/kg) intravenously immediately prior to initiation of Unituxin and then continue as a morphine sulfate drip at an infusion rate of 20 to 50 mcg/kg/hour during and for 2 hours following completion of Unituxin.
    • Administer additional 25 mcg/kg to 50 mcg/kg intravenous doses of morphine sulfate as needed for pain up to once every 2 hours followed by an increase in the morphine sulfate infusion rate in clinically stable patients.
    • Consider using fentanyl or hydromorphone if morphine sulfate is not tolerated.
    • If pain is inadequately managed with opioids, consider use of gabapentin or lidocaine in conjunction with intravenous morphine.

    Antihistamines and Antipyretics

    • Administer an antihistamine such as diphenhydramine (0.5 to 1 mg/kg; maximum dose 50 mg) intravenously over 10 to 15 minutes starting 20 minutes prior to initiation of Unituxin and as tolerated every 4 to 6 hours during the Unituxin infusion.
    • Administer acetaminophen (10 to 15 mg/kg; maximum dose 650 mg) 20 minutes prior to each Unituxin infusion and every 4 to 6 hours as needed for fever or pain. Administer ibuprofen (5 to 10 mg/kg) every 6 hours as needed for control of persistent fever or pain.

    2.3 Dosage Modifications

    Manage adverse reactions by infusion interruption, infusion rate reduction, dose reduction, or permanent discontinuation of Unituxin (Table 3 and Table 4) [see Warnings and Precautions (5), Adverse Reactions (6), and Clinical Studies (14)].

    Table 3: Adverse Reactions Requiring Permanent Discontinuation of Unituxin
    Grade 3 or 4 anaphylaxis
    Grade 3 or 4 serum sickness
    Grade 3 pain unresponsive to maximum supportive measures
    Grade 4 sensory neuropathy or Grade 3 sensory neuropathy that interferes with daily activities for more than 2 weeks
    Grade 2 or greater peripheral motor neuropathy
    Urinary retention that persists following discontinuation of opioids
    Transverse myelitis
    Reversible posterior leukoencephalopathy syndrome (RPLS)
    Subtotal or total vision loss
    Grade 4 hyponatremia despite appropriate fluid management
    Table 4: Dose Modification for Selected Unituxin Adverse Reactions
    *
    Symptomatic hypotension, systolic blood pressure (SBP) less than lower limit of normal for age, or SBP decreased by more than 15% compared to baseline.
    Infusion-related reactions [see Warnings and Precautions (5.1)]
    Mild to moderate adverse reactions, such as transient rash, fever, rigors, and localized urticaria, that respond promptly to symptomatic treatment
    Onset of reaction:Reduce Unituxin infusion rate to 50% of the previous rate and monitor closely.
    After resolution:Gradually increase infusion rate up to a maximum rate of 1.75 mg/m2/hour.
    Prolonged or severe adverse reactions, such as mild bronchospasm without other symptoms, or angioedema that does not affect the airway
    Onset of reaction: Immediately interrupt Unituxin.
    After resolution:If signs and symptoms resolve rapidly, resume Unituxin at 50% of the previous rate and observe closely.
    First recurrence:

    Discontinue Unituxin until the following day.

    If symptoms resolve and continued treatment is warranted, premedicate with hydrocortisone 1 mg/kg (maximum dose 50 mg) intravenously and administer Unituxin at a rate of 0.875 mg/m2/hour in an intensive care unit.
    Second recurrence:Permanently discontinue Unituxin.
    Neurological disorders of the eye [see Warnings and Precautions (5.2)]
    Onset of reaction:Discontinue Unituxin infusion until resolution.
    After resolution:Reduce the Unituxin dose by 50%.
    First recurrence or if accompanied by visual impairment:Permanently discontinue Unituxin.
    Capillary leak syndrome [see Warnings and Precautions (5.3)]
    Moderate to severe but not life-threatening capillary leak syndrome
    Onset of reaction:Immediately interrupt Unituxin.
    After resolution:Resume Unituxin infusion at 50% of the previous rate.
    Life-threatening capillary leak syndrome
    Onset of reaction:Discontinue Unituxin for the current cycle.
    After resolution:In subsequent cycles, administer Unituxin at 50% of the previous rate.
    First recurrence:Permanently discontinue Unituxin.
    Hypotension* requiring medical intervention [see Warnings and Precautions (5.4)]
    Onset of reaction:Interrupt Unituxin infusion.
    After resolution:

    Resume Unituxin infusion at 50% of the previous rate.

    If blood pressure remains stable for at least 2 hours, increase the infusion rate as tolerated up to a maximum rate of 1.75 mg/m2/hour.
    Severe systemic infection or sepsis [see Warnings and Precautions (5.5)]
    Onset of reaction:Discontinue Unituxin until resolution of infection, and then proceed with subsequent cycles of therapy.

    2.4 Instructions for Preparation and Administration

    Preparation

    • Store vials in a refrigerator at 2°C to 8°C (36°F to 46°F). Protect from light by storing in the outer carton. DO NOT FREEZE OR SHAKE vials.
    • Inspect visually for particulate matter and discoloration prior to administration. Do not administer Unituxin and discard the single-dose vial if the solution is cloudy, has pronounced discoloration, or contains particulate matter.
    • Aseptically withdraw the required volume of Unituxin from the single-dose vial and inject into a 100-mL bag of 0.9% Sodium Chloride Injection, USP. Mix by gentle inversion. Do not shake. Discard unused contents of the vial.
    • Store the diluted Unituxin solution under refrigeration (2°C to 8°C). Initiate infusion within 4 hours of preparation.
    • Discard diluted Unituxin solution 24 hours after preparation.

    Administration

    • Administer Unituxin as a diluted intravenous infusion only [see Dosage and Administration (2.1)]. Do not administer Unituxin as an intravenous push or bolus.
  • 3 DOSAGE FORMS AND STRENGTHS

    Injection: 17.5 mg/5 mL (3.5 mg/mL) as a clear and colorless to slightly opalescent solution in a single-dose vial.

  • 4 CONTRAINDICATIONS

    Unituxin is contraindicated in patients with a history of anaphylaxis to dinutuximab.

  • 5 WARNINGS AND PRECAUTIONS

    5.1 Serious Infusion Reactions

    Serious infusion reactions requiring urgent intervention, including blood pressure support, bronchodilator therapy, corticosteroids, infusion rate reduction, infusion interruption, or permanent discontinuation of Unituxin, included facial and upper airway edema, dyspnea, bronchospasm, stridor, urticaria, and hypotension. Infusion reactions generally occurred during or within 24 hours of completing the Unituxin infusion. Due to overlapping signs and symptoms, it was not possible to distinguish between infusion reactions and hypersensitivity reactions in some cases.

    In Study 1, Severe (Grade 3 or 4) infusion reactions occurred in 35 (26%) patients in the Unituxin/13-cis-retinoic acid (RA) group compared to 1 (1%) patient receiving RA alone. Severe urticaria occurred in 17 (13%) patients in the Unituxin/RA group but did not occur in the RA group. Serious adverse reactions consistent with anaphylaxis and resulting in permanent discontinuation of Unituxin occurred in 2 (1%) patients in the Unituxin/RA group. Additionally, 1 (0.1%) patient had multiple cardiac arrests and died within 24 hours after having received Unituxin in Study 2.

    Prior to each Unituxin dose, administer required intravenous hydration and premedication with antihistamines, analgesics, and antipyretics [see Dosage and Administration (2.2)]. Monitor patients closely for signs and symptoms of infusion reactions during and for at least 4 hours following completion of each Unituxin infusion in a setting where cardiopulmonary resuscitation medication and equipment are available.

    For mild to moderate infusion reactions, such as transient rash, fever, rigors, and localized urticaria, that respond promptly to antihistamines or antipyretics, decrease the Unituxin infusion rate and monitor closely. Immediately interrupt or permanently discontinue Unituxin and institute supportive management for severe or prolonged infusion reactions. Permanently discontinue Unituxin and institute supportive management for life-threatening infusion reactions [see Dosage and Administration (2.3)].

    5.2 Neurotoxicity

    Pain

    In Study 1, 114 (85%) patients treated in the Unituxin/RA group experienced pain despite pre-treatment with analgesics, including morphine sulfate infusion. Severe (Grade 3) pain occurred in 68 (51%) patients in the Unituxin/RA group compared to 5 (5%) patients in the RA group. Pain typically occurred during the Unituxin infusion and was most commonly reported as abdominal pain, generalized pain, extremity pain, back pain, neuralgia, musculoskeletal chest pain, and arthralgia.

    Premedicate with analgesics, including intravenous opioids, prior to each dose of Unituxin and continue analgesics until 2 hours following completion of Unituxin [see Dosage and Administration (2.2)].

    For severe pain, decrease the Unituxin infusion rate to 0.875 mg/m2/hour. Discontinue Unituxin if pain is not adequately controlled despite infusion rate reduction and institution of maximum supportive measures [see Dosage and Administration (2.3)].

    Peripheral Neuropathy

    In Study 1, severe (Grade 3) peripheral sensory neuropathy occurred in 2 (1%) patients and severe peripheral motor neuropathy occurred in 2 (1%) patients in the Unituxin/RA group. No patients treated with RA alone experienced severe peripheral neuropathy. The duration and reversibility of peripheral neuropathy occurring in Study 1 was not documented. In Study 3, no patients experienced peripheral motor neuropathy. Among the 9 (9%) patients who experienced peripheral sensory neuropathy of any severity, the median (min, max) duration of peripheral sensory neuropathy was 9 (3, 163) days.

    In a study of a related anti-GD2 antibody conducted in 12 adult patients with metastatic melanoma, 2 (13%) patients developed severe motor neuropathy. One patient developed lower extremity weakness and inability to ambulate that persisted for approximately 6 weeks. Another patient developed severe lower extremity weakness resulting in an inability to ambulate without assistance that lasted for approximately 16 weeks and neurogenic bladder that lasted for approximately 3 weeks. Complete resolution of motor neuropathy was not documented in this case.

    Permanently discontinue Unituxin in patients with peripheral motor neuropathy of Grade 2 or greater severity, Grade 3 sensory neuropathy that interferes with daily activities for more than 2 weeks, or Grade 4 sensory neuropathy [see Dosage and Administration (2.3)].

    Neurological Disorders of the Eye

    Neurological disorders of the eye experienced by 2 or more patients treated with Unituxin in Studies 1, 2, or 3 included blurred vision, photophobia, mydriasis, fixed or unequal pupils, optic nerve disorder, eyelid ptosis, and papilledema.

    In Study 1, 3 (2%) patients in the Unituxin/RA group experienced blurred vision, compared to no patients in the RA group. Diplopia, mydriasis, and unequal pupillary size occurred in 1 patient each in the Unituxin/RA group, compared to no patients in the RA group. The duration of eye disorders occurring in Study 1 was not documented. In Study 3, eye disorders occurred in 16 (15%) patients, and in 3 (3%) patients resolution of the eye disorder was not documented. Among the cases with documented resolution, the median duration of eye disorders was 4 days (range: 0, 221 days).

    Interrupt Unituxin in patients experiencing dilated pupil with sluggish light reflex or other visual disturbances that do not cause visual loss. Upon resolution and if continued treatment with Unituxin is warranted, decrease the Unituxin dose by 50%. Permanently discontinue Unituxin in patients with recurrent signs or symptoms of an eye disorder following dose reduction and in patients who experience loss of vision [see Dosage and Administration (2.3)].

    Prolonged Urinary Retention

    Urinary retention that persists for weeks to months following discontinuation of opioids has occurred in patients treated with Unituxin. Permanently discontinue Unituxin in patients with urinary retention that does not resolve following discontinuation of opioids [see Dosage and Administration (2.3) and Postmarketing Experience (6.3)].

    Transverse Myelitis

    Transverse myelitis has occurred in patients treated with Unituxin. Promptly evaluate any patient with signs or symptoms of transverse myelitis, such as weakness, paresthesia, sensory loss, or incontinence. Permanently discontinue Unituxin in patients who develop transverse myelitis [see Dosage and Administration (2.3) and Postmarketing Experience (6.3)].

    Reversible Posterior Leukoencephalopathy Syndrome

    Reversible Posterior Leukoencephalopathy Syndrome (RPLS) has occurred in patients treated with Unituxin. Institute appropriate medical treatment and permanently discontinue Unituxin in patients with signs and symptoms of RPLS (eg, severe headache, hypertension, visual changes, lethargy, or seizures) [see Dosage and Administration (2.3) and Postmarketing Experience (6.3)].

    5.3 Capillary Leak Syndrome

    In Study 1, severe (Grade 3 to 5) capillary leak syndrome occurred in 31 (23%) patients in the Unituxin/RA group and in no patients treated with RA alone. Additionally, capillary leak syndrome was reported as a serious adverse reaction in 9 (6%) patients in the Unituxin/RA group and in no patients treated with RA alone. Immediately interrupt or discontinue Unituxin and institute supportive management in patients with symptomatic or severe capillary leak syndrome [see Dosage and Administration (2.3)].

    5.4 Hypotension

    In Study 1, severe (Grade 3 or 4) hypotension occurred in 22 (16%) patients in the Unituxin/RA group compared to no patients in the RA group.

    Prior to each Unituxin infusion, administer required intravenous hydration. Closely monitor blood pressure during Unituxin treatment. Immediately interrupt or discontinue Unituxin and institute supportive management in patients with symptomatic hypotension, systolic blood pressure (SBP) less than lower limit of normal for age, or SBP that is decreased by more than 15% compared to baseline [see Dosage and Administration (2.2, 2.3)].

    5.5 Infection

    In Study 1, severe (Grade 3 or 4) bacteremia requiring intravenous antibiotics or other urgent intervention occurred in 17 (13%) patients in the Unituxin/RA group compared to 5 (5%) patients treated with RA alone. Sepsis occurred in 24 (18%) patients in the Unituxin/RA group and in 10 (9%) patients in the RA group.

    Monitor patients closely for signs and symptoms of systemic infection and temporarily discontinue Unituxin in patients who develop systemic infection until resolution of the infection [see Dosage and Administration (2.3)].

    5.6 Bone Marrow Suppression

    In Study 1, severe (Grade 3 or 4) thrombocytopenia (39% vs. 25%), anemia (34% vs. 16%), neutropenia (34% vs. 13%), and febrile neutropenia (4% vs. 0 patients) occurred more commonly in patients in the Unituxin/RA group compared to patients treated with RA alone. Monitor peripheral blood counts closely during therapy with Unituxin.

    5.7 Electrolyte Abnormalities

    In Study 1, electrolyte abnormalities occurring in at least 25% of patients who received Unituxin/RA included hyponatremia, hypokalemia, and hypocalcemia. Severe (Grade 3 or 4) hypokalemia and hyponatremia occurred in 37% and 23% of patients in the Unituxin/RA group, respectively, compared to 2% and 4% of patients in the RA group. In a study of a related anti-GD2 antibody conducted in 12 adult patients with metastatic melanoma, 2 (13%) patients developed syndrome of inappropriate antidiuretic hormone secretion resulting in severe hyponatremia. Monitor serum electrolytes daily during therapy with Unituxin.

    5.8 Atypical Hemolytic Uremic Syndrome

    Hemolytic uremic syndrome in the absence of documented infection and resulting in renal insufficiency, electrolyte abnormalities, anemia, and hypertension occurred in 2 patients enrolled in Study 2 following receipt of the first cycle of Unituxin. Atypical hemolytic uremic syndrome recurred following rechallenge with Unituxin in 1 patient. Permanently discontinue Unituxin and institute supportive management for signs of hemolytic uremic syndrome.

    5.9 Embryo-Fetal Toxicity

    Based on its mechanism of action, Unituxin may cause fetal harm when administered to a pregnant woman. Advise pregnant women of the potential risk to a fetus. Advise females of reproductive potential to use effective contraception during treatment, and for 2 months after the last dose of Unituxin [see Use in Specific Populations (8.1, 8.3) and Clinical Pharmacology (12.1)].

  • 6 ADVERSE REACTIONS

    The following adverse reactions are discussed in greater detail in other sections of the labeling:

    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 rates observed in clinical practice.

    The data described below reflect exposure to Unituxin at the recommended dose and schedule in 1021 patients with high-risk neuroblastoma enrolled in an open-label, randomized (Study 1), or single-arm clinical trials (Study 2 and Study 3). Prior to enrollment, patients received therapy consisting of induction combination chemotherapy, maximum feasible surgical resection, myeloablative consolidation chemotherapy followed by autologous stem cell transplant, and radiation therapy to residual soft tissue disease. Patients received Unituxin in combination with granulocyte-macrophage colony-stimulating factor (GM-CSF), interleukin-2 (IL-2), and 13-cis-retinoic acid (RA). Treatment commenced within 95 days post autologous stem cell transplant in Study 1, within 210 days of autologous stem cell transplant in Study 2, and within 110 days of autologous stem cell transplant in Study 3.

    Study 1

    In a randomized, open-label, multicenter study (Study 1), 134 patients received Unituxin in combination with GM-CSF, IL-2, and RA (Unituxin/RA group), including 109 randomized patients and 25 patients with biopsy-proven residual disease who were non-randomly assigned to receive Unituxin. A total of 106 randomized patients received RA alone (RA group) [see Dosage and Administration (2) and Clinical Studies (14)]. Patients had a median age at enrollment of 3.8 years (range: 0.94 to 15.3 years), and were predominantly male (60%) and White (82%). In Study 1, adverse reactions of Grade 3 or greater severity were comprehensively collected, but adverse reactions of Grade 1 or 2 severity were collected sporadically and laboratory data were not comprehensively collected.

    Approximately 71% of patients in the Unituxin/RA group and 77% of patients in the RA group completed planned treatment. The most common reason for premature discontinuation of study therapy was adverse reactions in the Unituxin/RA group (19%) and progressive disease (17%) in the RA group.

    The most common adverse drug reactions (≥25%) in the Unituxin/RA group were pain, pyrexia, thrombocytopenia, lymphopenia, infusion reactions, hypotension, hyponatremia, increased alanine aminotransferase, anemia, vomiting, diarrhea, hypokalemia, capillary leak syndrome, neutropenia, urticaria, hypoalbuminemia, increased aspartate aminotransferase, and hypocalcemia. The most common serious adverse reactions (≥5%) in the Unituxin/RA group were infections, infusion reactions, hypokalemia, hypotension, pain, fever, and capillary leak syndrome.

    Table 5 lists the adverse reactions reported in at least 10% of patients in the Unituxin/RA group for which there was a between group difference of at least 5% (all grades) or 2% (Grade 3 or greater severity).

    Table 5: Selected Adverse Reactions Occurring in at Least 10% of Patients in the Unituxin/RA Group in Study 1
    Adverse Reaction*,†Unituxin/RA
    (N=134)    		RA
    (N=106)
    All Grades
    (%)    		Grades 3 to 4
    (%)    		All Grades
    (%)    		Grades 3 to 4
    (%)
    *
    Includes adverse reactions that occurred in at least 10% of patients in the Unituxin/RA group with at least a 5% (All Grades) or 2% (Grades 3 to 5) absolute higher incidence in the Unituxin/RA group compared to the RA group.
    †
    Adverse drug reactions were graded using CTCAE version 3.0.
    ‡
    Includes preferred terms abdominal pain, abdominal pain upper, arthralgia, back pain, bladder pain, bone pain, chest pain, facial pain, gingival pain, infusion related reaction, musculoskeletal chest pain, myalgia, neck pain, neuralgia, oropharyngeal pain, pain, pain in extremity, and proctalgia.
    §
    Based on investigator reported adverse reactions.
    One Grade 5 adverse reaction.
    #
    Includes preferred terms gastrointestinal hemorrhage, hematochezia, rectal hemorrhage, hematemesis, upper gastrointestinal hemorrhage, hematuria, hemorrhage urinary tract, renal hemorrhage, epistaxis, respiratory tract hemorrhage, disseminated intravascular coagulation, catheter site hemorrhage, hemorrhage, and hematoma.
    Þ
    Includes preferred terms tachycardia and sinus tachycardia.
    General Disorders and Administration Site Conditions
      Pain‡8551166
      Pyrexia7240276
      Edema17000
    Blood and Lymphatic System Disorders§
      Thrombocytopenia66394325
      Lymphopenia§62513620
      Anemia51342216
      Neutropenia39341613
    Immune System Disorders
      Infusion reactions602591
    Vascular Disorders
      Hypotension601630
      Capillary leak syndrome402310
      Hemorrhage#17663
      Hypertension14271
    Metabolism and Nutrition Disorders
      Hyponatremia§5823124
      Hypokalemia§433742
      Hypoalbuminemia§33730
      Hypocalcemia§27700
      Hypophosphatemia§20830
      Hyperglycemia§18641
      Hypertriglyceridemia§161111
      Decreased appetite151054
      Hypomagnesemia§12210
    Investigations
      Increased alanine aminotransferase§5623313
      Increased aspartate aminotransferase§281070
      Increased serum creatinine§15260
      Increased weight10000
    Gastrointestinal Disorders
      Vomiting466193
      Diarrhea4313151
      Nausea10231
    Skin and Subcutaneous Tissue Disorders
      Urticaria371330
    Respiratory, Thoracic and Mediastinal Disorders
      Hypoxia241221
    Cardiac Disorders
      TachycardiaÞ19210
    Infections and Infestations
      Sepsis181699
      Device related infection16161111
    Renal and Urinary Disorders
      Proteinuria§16031
    Nervous System Disorders
      Peripheral neuropathy13360

    Table 6 compares the per-patient incidence of selected adverse reactions occurring during cycles containing Unituxin in combination with GM-CSF (Cycles 1, 3, and 5) with cycles containing Unituxin in combination with IL-2 (Cycles 2 and 4).

    Table 6: Comparison of Adverse Events by Treatment Cycle in the Unituxin/RA Group in Study 1
    Preferred Term*,†All GradesSevere
    GM-CSF
    N=134
    (%)    		IL-2‡
    N=127
    (%)    		GM-CSF
    N=134
    (%)    		IL-2‡
    N=127
    (%)
    GM-CSF, granulocyte-macrophage colony-stimulating factor; IL-2, interleukin-2; RA, 13-cis-retinoic acid
    *
    Includes preferred terms with a per-patient incidence of at least 20% in the Unituxin and RA group for either IL-2 or GM-CSF containing cycles.
    †
    Adverse drug reactions were graded using CTCAE version 3.0.
    ‡
    Seven patients who received GM-CSF in Cycle 1 discontinued prior to starting Cycle 2.
    §
    Includes preferred terms abdominal pain, abdominal pain upper, arthralgia, back pain, bladder pain, bone pain, chest pain, facial pain, gingival pain, infusion related reaction, musculoskeletal chest pain, myalgia, neck pain, neuralgia, oropharyngeal pain, pain, pain in extremity, and proctalgia.
    Based on investigator-reported adverse reactions.
    General Disorders and administration site conditions
      Pyrexia55651037
      Pain§77614335
    Blood and Lymphatic System Disorders
      Thrombocytopenia62613133
      Lymphopenia54613350
      Anemia42422124
      Neutropenia25321928
    Immune System Disorders
      Infusion reactions47541020
    Vascular Disorders
      Hypotension4354516
      Capillary leak syndrome22361120
    Metabolism and Nutrition Disorders
      Hyponatremia3655521
      Hypokalemia26391333
      Hypoalbuminemia292935
      Hypocalcemia202126
    Investigations
      Increased alanine aminotransferase43481513
      Aspartate aminotransferase increased162147
    Gastrointestinal Disorders
      Diarrhea3137613
      Vomiting333532
    Skin and Subcutaneous Tissue Disorders
      Urticaria252977

    Study 2 and Study 3

    Study 2 was a single-arm, multicenter, expanded access trial that enrolled patients with high-risk neuroblastoma (N=783). The reported adverse event profile of Unituxin in Study 2 was similar to that observed in Study 1.

    Study 3 was a multicenter, single-arm safety study of Unituxin in combination with GM-CSF, IL-2, and RA. In Study 3, adverse events of all CTCAE grades and laboratory data were systematically and comprehensively collected. Of 104 patients enrolled and treated in Study 3, 77% of patients completed study therapy. In general, the adverse reaction profile of Unituxin observed in Study 3 was similar to that observed in Study 1 and Study 2. The following adverse reactions not previously reported in Study 1 were reported in at least 10% of patients in Study 3: nasal congestion (20%) and wheezing (15%). Table 7 provides the per-patient incidence of laboratory abnormalities in Study 3.

    Table 7: Per-patient Incidence of Selected (≥5% Grade 3 to 4) Laboratory Abnormalities in Study 3
    Laboratory Test*Grade†
    All Grades %Grades 3 to 4 %
    ND, not determined
    *
    Laboratory abnormalities with a per-patient incidence of at least 20% (all grades) and at least a 5% per-patient incidence of severe (Grade 3 or 4) laboratory abnormalities.
    †
    Based on CTCAE version 4.0.
    ‡
    Urinalysis results were reported as positive or negative without assessment of grade.
    Hematology
      Anemia10046
      Neutropenia9963
      Thrombocytopenia9849
    Chemistry
      Hypoalbuminemia1008
      Hypocalcemia977
      Hyponatremia9336
      Hyperglycemia876
      Aspartate Aminotransferase Increased848
      Alanine Aminotransferase Increased8313
      Hypokalemia8241
      Hypophosphatemia786
    Urinalysis‡
      Urine protein66ND
      Red blood cell casts38ND

    6.2 Immunogenicity

    As with all therapeutic proteins, there is a potential for immunogenicity. The detection of antibody formation is highly dependent on the sensitivity and specificity of the assay.

    Additionally, the observed incidence of antibody (including neutralizing antibody) positivity in an assay may be influenced by several factors, including assay methodology, sample handling, timing of sample collection, concomitant medications, and underlying disease. For these reasons, comparison of the incidence of antibodies in the studies described below with the incidence of antibodies in other studies or to other products may be misleading.

    Among the 418 patients who were treated with Unituxin in combination with GM-CSF, IL-2, and RA in Study 2, Study 3 and Study DIV-NB-201, 86 patients (20.6%) tested positive for anti-dinutuximab antibodies (ADA). Of the 86 ADA positive patients, 45 (52.3%) tested positive for neutralizing antibodies.

    Among the 27 patients who were treated with Unituxin in combination with lenalidomide and isotretinoin in Study NANT 2011-04, 13 patients (48.1%) tested positive for ADA. Of the 13 ADA positive patients, 2 (15.4%) also tested positive for neutralizing antibodies.

    The clearance of dinutuximab was 60% higher for the ADA positive patients than the ADA negative patients. The presence of ADA did not have a clinically significant effect on the incidence or severity of adverse reactions. There were insufficient number of patients with ADA to determine whether ADA alters the efficacy of Unituxin.

    6.3 Postmarketing Experience

    The following adverse reactions have been identified during post-approval use of Unituxin. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.

    • Neurotoxicity: prolonged urinary retention, transverse myelitis, and reversible posterior leukoencephalopathy syndrome (RPLS) [see Warnings and Precautions (5.2)].
  • 7 DRUG INTERACTIONS

    No drug-drug interaction studies have been conducted with dinutuximab.

  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Risk Summary

    Based on its mechanism of action, Unituxin may cause fetal harm when administered to a pregnant woman [see Clinical Pharmacology (12.1)]. There are no studies in pregnant women and no reproductive studies in animals to inform the drug-associated risk. Monoclonal antibodies are transported across the placenta in a linear fashion as pregnancy progresses, with the largest amount transferred during the third trimester. Advise pregnant women of the potential risk to a fetus. The background risk of major birth defects and miscarriage for the indicated population is unknown. However, the background risk in the U.S. general population of major birth defects is 2 to 4% and of miscarriage is 15 to 20% of clinically recognized pregnancies.

    8.2 Lactation

    Risk Summary

    There is no information available on the presence of dinutuximab in human milk, the effects of the drug on the breastfed infant, or the effects of the drug on milk production. However, human IgG is present in human milk. Because of the potential for serious adverse reactions in a breastfed infant, advise a nursing woman to discontinue breastfeeding during treatment with Unituxin.

    8.3 Females and Males of Reproductive Potential

    Contraception

    Females

    Unituxin may cause fetal harm [see Use in Specific Populations (8.1)]. Advise females of reproductive potential to use effective contraception during treatment and for 2 months after the last dose of Unituxin.

    8.4 Pediatric Use

    The safety and effectiveness of Unituxin as part of multi-agent, multimodality therapy have been established in pediatric patients with high-risk neuroblastoma based on results of an open-label, randomized (1:1) trial conducted in 226 patients aged 11 months to 15 years (median age 3.8 years) (Study 1). Prior to enrollment, patients achieved at least a partial response to prior first-line therapy for high-risk neuroblastoma consisting of induction combination chemotherapy, maximum feasible surgical resection, myeloablative consolidation chemotherapy followed by autologous stem cell transplant, and received radiation therapy to residual soft tissue disease. Patients randomized to the Unituxin/13-cis-retinoic acid (RA) arm (Unituxin/RA) received up to 5 cycles of Unituxin in combination with alternating cycles of granulocyte-macrophage colony-stimulating factor (GM-CSF) and interleukin-2 (IL-2) plus RA, followed by 1 cycle of RA alone. Patients randomized to the RA arm received up to 6 cycles of RA monotherapy. Study 1 demonstrated an improvement in event-free survival (EFS) and overall survival (OS) in patients in the Unituxin/RA arm compared to those in the RA arm [see Adverse Reactions (6), Clinical Pharmacology (12), and Clinical Studies (14)].

    Juvenile Animal Toxicity Data

    Juvenile monkeys (13 to 18 months of age at study start) received dinutuximab daily via intravenous infusion for 4 consecutive days over five 28-day cycles at doses of 1, 3, or 10 mg/kg. Monkeys also received morphine during infusion for pain management. At the high dose of 10 mg/kg (approximately equal to the 17.5 mg/m2 clinical dose), mild degeneration of nerve fibers in the brain (medulla oblongata) and moderate degeneration of nerve fibers in the spinal cord (cervical, thoracic, and lumbar) were present. Mild neuronal and nerve fiber degeneration were also present in the dorsal root ganglia (cervical, thoracic, and lumbar). Nerve fiber degeneration in the spinal cord and neuronal degeneration in dorsal root ganglia persisted 6 months after the end of dosing, though at lower severity. At the 10 mg/kg dose level, nerve conduction velocity (NCV) analysis showed motor and sensory NCV decreases of less than 10% compared to vehicle controls, starting on Day 27 and continuing to Day 83. Sensory NCV decreases were still present at the end of the dosing period but were on a trend towards recovery 6 months after the end of dosing.

    8.5 Geriatric Use

    The safety and effectiveness of Unituxin in geriatric patients have not been established.

    8.6 Renal Impairment

    Unituxin has not been studied in patients with renal impairment.

    8.7 Hepatic Impairment

    Unituxin has not been studied in patients with hepatic impairment.

  • 11 DESCRIPTION

    Dinutuximab is a glycolipid disialoganglioside (GD2)-binding chimeric monoclonal antibody composed of murine variable heavy and light chain regions and the human constant region for the heavy chain IgG1 and light chain kappa. Dinutuximab is produced in the murine myeloma cell line, SP2/0 and has an approximate molecular weight of 150 kDa.

    Unituxin (dinutuximab) injection is a sterile, preservative-free, clear and colorless to slightly opalescent solution for intravenous infusion. Unituxin is supplied in single-dose vials of 17.5 mg/5 mL. Each mL of solution contains 3.5 mg of dinutuximab, and histidine (3.10 mg), polysorbate 20 (0.55 mg), sodium chloride (8.77 mg), and Water for Injection, USP; hydrochloric acid is added to adjust pH to 6.8.

  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    Dinutuximab binds to the glycolipid GD2. This glycolipid is expressed on neuroblastoma cells and on normal cells of neuroectodermal origin, including the central nervous system and peripheral nerves. Dinutuximab binds to cell surface GD2 and induces cell lysis of GD2-expressing cells through antibody-dependent cell-mediated cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC).

    12.3 Pharmacokinetics

    The pharmacokinetics of dinutuximab was evaluated by a population pharmacokinetic analysis in a clinical study of Unituxin in combination with GM-CSF, IL-2, and RA. In this study, 27 children with high-risk neuroblastoma (age: 3.9±1.9 years) received up to 5 cycles of Unituxin at 17.5 mg/m2/day as an intravenous infusion over 10 to 20 hours for 4 consecutive days every 28 days. The observed maximum plasma dinutuximab concentration (Cmax) was 11.5 mcg/mL (20%, coefficient of variation [CV]). The mean volume of distribution at steady state (Vdss) was 5.4 L (28%). The clearance was 0.21 L/day (62%) and increased with body size. The terminal half-life was 10 days (56%).

    No formal pharmacokinetic studies were conducted in patients with renal or hepatic impairment.

  • 13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    No animal studies have been conducted to evaluate the carcinogenic or mutagenic potential of dinutuximab.

    Dedicated studies examining the effects of dinutuximab on fertility in animals have not been conducted. No clear effects on reproductive organs were observed in general toxicology studies conducted in rats.

    13.2 Animal Toxicology and/or Pharmacology

    Nonclinical studies suggest that dinutuximab-induced neuropathic pain and neurotoxicity are mediated by binding of the antibody to the GD2 antigen located on the surface of nerve fibers and myelin and subsequent induction of CDC and ADCC activity.

  • 14 CLINICAL STUDIES

    The safety and effectiveness of Unituxin was evaluated in a randomized, open-label, multicenter trial conducted in pediatric patients with high-risk neuroblastoma (Study 1). All patients had received prior therapy consisting of induction combination chemotherapy, maximum feasible surgical resection, myeloablative consolidation chemotherapy followed by autologous stem cell transplant, and radiation therapy to residual soft tissue disease. Patients were randomized between Day 50 and Day 77 post-autologous stem cell transplantation.

    Patients were required to have achieved at least a partial response prior to autologous stem cell transplantation, have no evidence of disease progression following completion of front-line multi-modality therapy, have adequate pulmonary function (no dyspnea at rest and peripheral arterial oxygen saturation of at least 94% on room air), adequate hepatic function (total bilirubin <1.5× the upper limit of normal and ALT <5× the upper limit of normal), adequate cardiac function (shortening fraction of >30% by echocardiogram, or if shortening fraction abnormal, ejection fraction of 55% by gated radionuclide study), and adequate renal function (glomerular filtration rate at least 70 mL/min/1.73 m2). Patients with systemic infections or a requirement for concomitant systemic corticosteroids or immunosuppressant usage were not eligible for enrollment.

    Patients randomized to the Unituxin/RA arm received up to 5 cycles of Unituxin (clinical trials material) in combination with granulocyte-macrophage colony-stimulating factor (GM-CSF) (Table 8) or interleukin-2 (IL-2) (Table 9) plus 13-cis-retinoic acid (RA), followed by 1 cycle of RA alone. Patients randomized to the RA arm received 6 cycles of RA. Unituxin was administered at a dose of 17.5 mg/m2/day (equivalent to 25 mg/m2/day of clinical trials material) on 4 consecutive days. Patients in both treatment arms received 6 cycles of RA at a dose of 160 mg/m2/day orally (for patients weighing more than 12 kg) or 5.33 mg/kg/day (for patients weighing less than or equal to 12 kg) in 2 divided doses for 14 consecutive days.

    Table 8: Dosage Regimen in the Unituxin/RA Arm for Cycles 1, 3, and 5
    Cycle Day123456789101112131415-24
    *
    GM-CSF: 250 µg/m2/day, administered by either subcutaneous injection (recommended) or IV infusion administered over 2 hours.
    †
    Unituxin: 17.5 mg/m2/day, administered by diluted IV infusion over 10 to 20 hours.
    ‡
    RA: for >12 kg body weight, 80 mg/m2 orally twice daily for a total dose of 160 mg/m2/day; for ≤12 kg body weight, 2.67 mg/kg orally twice daily for a total daily dose of 5.33 mg/kg/day (round dose up to nearest 10 mg).
    GM-CSF*XXXXXXXXXXXXXX
    Unituxin†XXXX
    RA‡XXXXX
    Table 9: Dosage Regimen in the Unituxin/RA Arm for Cycles 2 and 4
    Cycle Day123456789101112-1415-2829-32
    *
    IL-2: 3 MIU/m2/day administered by continuous IV infusion over 96 hours on Days 1 to 4 and 4.5 MIU/m2/day on Days 8 to 11.
    †
    Unituxin: 17.5 mg/m2/day, administered by diluted IV infusion over 10 to 20 hours.
    ‡
    RA: for >12 kg body weight, 80 mg/m2 orally twice daily for a total dose of 160 mg/m2/day; for ≤12 kg body weight, 2.67 mg/kg orally twice daily for a total daily dose of 5.33 mg/kg/day (round dose up to nearest 10 mg).
    IL-2*XXXXXXXX
    Unituxin†XXXX
    RA‡X

    A total of 226 patients were randomized, 113 patients to each arm. In general, demographic and baseline tumor characteristics were similar across study arms. Across the study population, 60% were male, the median age was 3.8 years and 3% of patients were less than 1.5 years, 82% were White and 7% were Black. The majority (80%) of patients had International Neuroblastoma Staging System Stage 4 disease. Thirty-five percent of patients had a complete response, 43% had a very good partial response, and 23% had a partial response to therapy received prior to autologous stem cell transplant. Forty-six percent of patients had neuroblastoma that was not MYCN-amplified, 36% had tumors with known MYCN-amplification, and MYCN status was unknown or missing in 19% of patients. Forty-three percent of patients had hyperdiploid tumors, 36% had diploid tumors, and DNA ploidy status was unknown or missing in 21% of patients.

    The major efficacy outcome measure was investigator-assessed event-free survival (EFS), defined as the time from randomization to the first occurrence of relapse, progressive disease, secondary malignancy, or death. Overall survival (OS) was also evaluated. After observing a numerical improvement in EFS based on the seventh interim analysis, the Data Monitoring Committee recommended termination of accrual. Efficacy results are shown in Table 10.

    Table 10: Efficacy Results
    Efficacy ParameterUnituxin/RA arm
    n=113    		RA arm
    n=113
    NR, not reached
    *
    Compared to the allocated alpha of 0.01 pre-specified for the seventh interim analysis of EFS
    †
    Based on an additional 3 years of follow up after the seventh interim analysis of EFS
    EFSNo. of Events (%)33 (29%)50 (44%)
    Median (95% CI) (years)NR (3.4, NR)1.9 (1.3, NR)
      Hazard Ratio (95% CI)0.57 (0.37, 0.89)
      p-value (log-rank test)*0.01
    OS†No. of Events (%)31 (27%) 48 (42%)
    Median (95% CI) (years)NR (7.5, NR)NR (3.9, NR)
      Hazard Ratio (95% CI)0.58 (0.37, 0.91)

    The Kaplan-Meier curve of EFS is shown in Figure 1.

    Figure 1: Kaplan-Meier Curve of Event-Free Survival

    Figure 1

  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    Unituxin (dinutuximab) injection as a clear and colorless to slightly opalescent solution is supplied in a carton containing one 17.5 mg/5 mL (3.5 mg/mL) single-dose vial.

    NDC 66302-014-01

    Store Unituxin vials under refrigeration at 2°C to 8°C (36°F to 46°F) in the outer carton to protect from light until time of use. Do not freeze or shake the vial.

  • 17 PATIENT COUNSELING INFORMATION

    • Serious Infusion Reactions
      Inform patients and caregivers of the risk of serious infusion reactions and anaphylaxis and to immediately report any signs or symptoms, such as facial or lip swelling, urticaria, difficulty breathing, lightheadedness, or dizziness that occur during or within 24 hours following the infusion [see Warnings and Precautions (5.1)].
    • Pain, Peripheral Neuropathy, Prolonged Urinary Retention, and Transverse Myelitis
      Inform patients and caregivers of the risk of severe pain, sensory and motor neuropathy, prolonged urinary retention, and transverse myelitis, and to promptly report severe or worsening pain and signs and symptoms, such as numbness, tingling, burning, weakness, or inability to urinate [see Warnings and Precautions (5.2)].
    • Neurological Disorders of the Eye
      Inform patients and caregivers of the risk of neurological disorders of the eye and to promptly report signs or symptoms, such as blurred vision, photophobia, ptosis, diplopia, or unequal pupil size [see Warnings and Precautions (5.2)].
    • Reversible Posterior Leukoencephalopathy Syndrome (RPLS)
      Inform patients and caregivers of the risk of RPLS and to immediately report signs or symptoms, such as severe headache, hypertension, visual changes, lethargy, or seizures [see Warnings and Precautions (5.2)].
    • Capillary Leak Syndrome
      Inform patients and caregivers of the risk of capillary leak syndrome and to immediately report any signs or symptoms [see Warnings and Precautions (5.3)].
    • Hypotension
      Inform patients and caregivers of the risk of hypotension during the infusion and to immediately report any signs or symptoms [see Warnings and Precautions (5.4)].
    • Infection
      Inform patients and caregivers of the risk of infection following treatment and to immediately report any signs or symptoms [see Warnings and Precautions (5.5)].
    • Bone Marrow Suppression
      Inform patients and caregivers of the risk of bone marrow suppression, and to promptly report signs or symptoms of anemia, thrombocytopenia, or infection [see Warnings and Precautions (5.6)].
    • Electrolyte Abnormalities
      Inform patients and caregivers of the risk of electrolyte abnormalities, including hypokalemia, hyponatremia, and hypocalcemia, and to report any signs or symptoms, such as seizures, heart palpitations, and muscle cramping [see Warnings and Precautions (5.7)].
    • Atypical Hemolytic Uremic Syndrome
      Inform patients and caregivers of the risk of hemolytic uremic syndrome and to report any signs or symptoms, such as fatigue, dizziness, fainting, pallor, edema, decreased urine output, or hematuria [see Warnings and Precautions (5.8)].
    • Embryo-Fetal Toxicity
      Advise women of reproductive potential of the potential risk to the fetus if administered during pregnancy and the need for use of effective contraception during and for at least 2 months after completing therapy [see Warnings and Precautions (5.9)].
  • SPL UNCLASSIFIED SECTION

    ®Copyright 2020 United Therapeutics Corp. All rights reserved.

    Unituxin manufactured by:

    United Therapeutics Corp.
    Research Triangle Park, NC 27709
    US License No. 1993

  • PRINCIPAL DISPLAY PANEL - 5 mL Vial Box

    NDC 66302-014-01

    Unituxin®
    (dinutuximab)
    Injection

    17.5 mg/5 mL
    (3.5 mg/mL)

    For Intravenous Infusion Only
    Dilute Prior to Administration

    Single-Dose Vial
    Discard Unused Portion
    Rx Only

    PRINCIPAL DISPLAY PANEL - 5 mL Vial Box
  • INGREDIENTS AND APPEARANCE
    UNITUXIN 
    dinutuximab injection
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:66302-014
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DINUTUXIMAB (UNII: 7SQY4ZUD30) (DINUTUXIMAB - UNII:7SQY4ZUD30) DINUTUXIMAB3.5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    histidine (UNII: 4QD397987E)  
    polysorbate 20 (UNII: 7T1F30V5YH)  
    sodium chloride (UNII: 451W47IQ8X)  
    water (UNII: 059QF0KO0R)  
    hydrochloric acid (UNII: QTT17582CB)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66302-014-011 in 1 BOX03/10/2015
    15 mL in 1 VIAL, SINGLE-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA12551603/10/2015
    Labeler - United Therapeutics Corporation (965460025)
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