`• For injectable suspension: lyophilized powder containing 100 mg of
`paclitaxel formulated as albumin-bound particles in single-use vial for
`reconstitution. (3)
` ------------------------------ CONTRAINDICATIONS -----------------------------
`• Neutrophil counts of < 1,500 cells/mm3. (4)
`• Severe hypersensitivity reaction to ABRAXANE. (4)
` ----------------------- WARNINGS AND PRECAUTIONS ----------------------
`• ABRAXANE causes myelosuppression. Monitor CBC and withhold
`and/or reduce the dose as needed. (5.1)
`• Sensory neuropathy occurs frequently and may require dose
`reduction or treatment interruption. (5.2)
`• Sepsis occurred in patients with or without neutropenia who received
`ABRAXANE in combination with gemcitabine; interrupt ABRAXANE
`and gemcitabine until sepsis resolves, and if neutropenia, until
`neutrophils are at least 1500 cells/mm3, then resume treatment at
`reduced dose levels. (5.3)
`• Pneumonitis occurred with the use of ABRAXANE in combination
`with gemcitabine; permanently discontinue treatment with
`ABRAXANE and gemcitabine. (5.4)
`• Severe hypersensitivity reactions with fatal outcome have been
`reported. Do not re-challenge with this drug. (5.5)
`• Exposure and toxicity of paclitaxel can be increased in patients with
`hepatic impairment; therefore administer with caution. (5.6)
`• ABRAXANE contains albumin derived from human blood, which has
`a theoretical risk of viral transmission. (5.7)
`• Fetal harm may occur when administered to a pregnant woman.
`Advise women of childbearing potential to avoid becoming pregnant
`while receiving ABRAXANE. (5.8)
`• Advise men not to father a child while on ABRAXANE. (5.9)
` ------------------------------ ADVERSE REACTIONS -----------------------------
`• The most common adverse reactions (≥ 20%) in metastatic breast
`cancer are alopecia, neutropenia, sensory neuropathy, abnormal
`ECG, fatigue/asthenia, myalgia/arthralgia, AST elevation, alkaline
`phosphatase elevation, anemia, nausea, infections, and
`diarrhea. (6.1)
`• The most common adverse reactions (≥ 20%) in NSCLC are anemia,
`neutropenia, thrombocytopenia, alopecia, peripheral neuropathy,
`nausea, and fatigue. (6.2)
`• The most common (≥ 20%) adverse reactions of ABRAXANE in
`adenocarcinoma of the pancreas are neutropenia, fatigue, peripheral
`neuropathy, nausea, alopecia, peripheral edema, diarrhea, pyrexia,
`vomiting, decreased appetite, rash, and dehydration. (6.3)
`
`
`To report SUSPECTED ADVERSE REACTIONS, contact Celgene
`Corporation at 1-888-423-5436 or FDA at 1-800-FDA-1088 or
`www.fda.gov/medwatch.
` ------------------------------ DRUG INTERACTIONS ------------------------------
`• Use caution when concomitantly administering ABRAXANE with
`inhibitors or inducers of either CYP2C8 or CYP3A4. (7)
`
`
`See 17 for PATIENT COUNSELING INFORMATION and
`FDA-approved patient labeling.
`
`
`Revised: 07/2015
`
`HIGHLIGHTS OF PRESCRIBING INFORMATION
`These highlights do not include all the information needed to use
`ABRAXANE safely and effectively. See full prescribing
`information for ABRAXANE.
`
`ABRAXANE® for Injectable Suspension (paclitaxel protein-bound
`particles for injectable suspension)
`(albumin-bound)
`Initial U.S. Approval: 2005
`
`
`WARNING: NEUTROPENIA
`See full prescribing information for complete boxed warning.
`
` Do not administer ABRAXANE therapy to patients with
`baseline neutrophil counts of less than 1,500 cells/mm3. (4)
`• It is recommended that frequent peripheral blood cell counts
`be performed to monitor the occurrence of bone marrow
`suppression. (4, 5.1, 6.1, 6.2, 6.3)
`DO NOT SUBSTITUTE FOR OR WITH OTHER PACLITAXEL
`FORMULATIONS.
` -------------------------- RECENT MAJOR CHANGES --------------------------
`• Dosage and Administration (2.4, 2.8)
`12/2014
`• Dosage and Administration (2.7)
`07/2015
`• Warnings and Precautions, Hepatic Impairment (5.6)
`12/2014
` -------------------------- INDICATIONS AND USAGE ----------------------------
`ABRAXANE is a microtubule inhibitor indicated for the treatment of:
`• Metastatic breast cancer, after failure of combination chemotherapy
`for metastatic disease or relapse within 6 months of adjuvant
`chemotherapy. Prior therapy should have included an anthracycline
`unless clinically contraindicated. (1.1)
`• Locally advanced or metastatic non-small cell lung cancer (NSCLC),
`as first-line treatment in combination with carboplatin, in patients who
`are not candidates for curative surgery or radiation therapy. (1.2)
`• Metastatic adenocarcinoma of the pancreas as first-line treatment, in
`combination with gemcitabine. (1.3)
` ----------------------- DOSAGE AND ADMINISTRATION ----------------------
`• Metastatic Breast Cancer: Recommended dosage of ABRAXANE is
`260 mg/m2 intravenously over 30 minutes every 3 weeks. (2.1)
`• Non-Small Cell Lung Cancer: Recommended dosage of ABRAXANE
`is 100 mg/m2 intravenously over 30 minutes on Days 1, 8, and 15 of
`each 21-day cycle; administer carboplatin on Day 1 of each 21-day
`cycle immediately after ABRAXANE. (2.2)
`• Adenocarcinoma of the Pancreas: Recommended dosage of
`ABRAXANE is 125 mg/m2 intravenously over 30-40 minutes on Days
`1, 8 and 15 of each 28-day cycle; administer gemcitabine on Days 1,
`8 and 15 of each 28-day cycle immediately after ABRAXANE. (2.3)
`• Do not administer ABRAXANE to any patient with AST > 10 x ULN or
`bilirubin > 5 x ULN. Do not administer ABRAXANE to patients with
`metastatic adenocarcinoma of the pancreas who have moderate to
`severe hepatic impairment. For diseases other than metastatic
`adenocarcinoma of the pancreas, reduce starting dose in patients
`with moderate to severe hepatic impairment. (2.4)
`• Dose Reductions: Dose reductions or discontinuation may be
`needed based on severe hematologic, neurologic, cutaneous, or
`gastrointestinal toxicities. (2.5)
`• Use caution when handling cytotoxic drugs. Closely monitor the
`infusion site for extravasation and infiltration. No premedication is
`required prior to administration. (2.6)
`
` •
`
`
`
`
`
`
`Reference ID: 3793488
`
`1
`
`
`
`6.4 Postmarketing Experience with ABRAXANE and other
`Paclitaxel Formulations
`6.5 Accidental Exposure
`7 DRUG INTERACTIONS
`8 USE IN SPECIFIC POPULATIONS
`8.1 Pregnancy
`8.3 Nursing Mothers
`8.4 Pediatric Use
`8.5 Geriatric Use
`8.6 Patients with Hepatic Impairment
`8.7 Patients with Renal Impairment
`10 OVERDOSAGE
`11 DESCRIPTION
`12 CLINICAL PHARMACOLOGY
`12.1 Mechanism of Action
`12.3 Pharmacokinetics
`13 NONCLINICAL TOXICOLOGY
`13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility
`14 CLINICAL STUDIES
`14.1 Metastatic Breast Cancer
`14.2 Non-Small Cell Lung Cancer
`14.3 Adenocarcinoma of the Pancreas
`15 REFERENCES
`16 HOW SUPPLIED/STORAGE AND HANDLING
`16.1 How Supplied
`16.2 Storage
`16.3 Handling and Disposal
`17 PATIENT COUNSELING INFORMATION
`
`
` *
`
` Sections or subsections omitted from the Full Prescribing Information
`are not listed.
`
`FULL PRESCRIBING INFORMATION: CONTENTS*
`
`WARNING: NEUTROPENIA
`1
`INDICATIONS AND USAGE
`1.1 Metastatic Breast Cancer
`1.2 Non-Small Cell Lung Cancer
`1.3 Adenocarcinoma of the Pancreas
`2 DOSAGE AND ADMINISTRATION
`2.1 Metastatic Breast Cancer
`2.2 Non-Small Cell Lung Cancer
`2.3 Adenocarcinoma of the Pancreas
`2.4 Dosage in Patients with Hepatic Impairment
`2.5 Dose Reduction/Discontinuation Recommendations
`2.6 Preparation and Administration Precautions
`2.7 Preparation for Intravenous Administration
`2.8 Stability
`3 DOSAGE FORMS AND STRENGTHS
`4 CONTRAINDICATIONS
`5 WARNINGS AND PRECAUTIONS
`5.1 Hematologic Effects
`5.2 Nervous System
`5.3 Sepsis
`5.4 Pneumonitis
`5.5 Hypersensitivity
`5.6 Hepatic Impairment
`5.7 Albumin (Human)
`5.8 Use in Pregnancy
`5.9 Use in Men
`6 ADVERSE REACTIONS
`6.1 Clinical Trials Experience in Metastatic Breast Cancer
`6.2 Clinical Trials Experience in Non-Small Cell Lung Cancer
`6.3 Clinical Trials Experience in Adenocarcinoma of the
`Pancreas
`
`
`
`
`
`
`Reference ID: 3793488
`
`2
`
`
`
`FULL PRESCRIBING INFORMATION
`ABRAXANE® for Injectable Suspension (paclitaxel protein-bound particles for injectable suspension) (albumin-bound)
`
`
`WARNING: NEUTROPENIA
`• Do not administer ABRAXANE therapy to patients who have baseline neutrophil counts of less than 1,500
`cells/mm3. In order to monitor the occurrence of bone marrow suppression, primarily neutropenia, which
`may be severe and result in infection, it is recommended that frequent peripheral blood cell counts be
`performed on all patients receiving ABRAXANE [see Contraindications (4), Warnings and Precautions (5.1)
`and Adverse Reactions (6.1, 6.2, 6.3)].
`
`• Note: An albumin form of paclitaxel may substantially affect a drug’s functional properties relative to those
`of drug in solution. DO NOT SUBSTITUTE FOR OR WITH OTHER PACLITAXEL FORMULATIONS.
`
`
`
`INDICATIONS AND USAGE
`
` 1
`
`
`Metastatic Breast Cancer
`1.1
`ABRAXANE is indicated for the treatment of breast cancer after failure of combination chemotherapy for metastatic disease or
`relapse within 6 months of adjuvant chemotherapy. Prior therapy should have included an anthracycline unless clinically
`contraindicated.
`
`Non-Small Cell Lung Cancer
`1.2
`ABRAXANE is indicated for the first-line treatment of locally advanced or metastatic non-small cell lung cancer, in combination with
`carboplatin, in patients who are not candidates for curative surgery or radiation therapy.
`
`Adenocarcinoma of the Pancreas
`1.3
`ABRAXANE is indicated for the first-line treatment of patients with metastatic adenocarcinoma of the pancreas, in combination with
`gemcitabine.
`
` 2
`
`
`
`DOSAGE AND ADMINISTRATION
`
`
`Metastatic Breast Cancer
`2.1
`After failure of combination chemotherapy for metastatic breast cancer or relapse within 6 months of adjuvant chemotherapy, the
`recommended regimen for ABRAXANE is 260 mg/m2 administered intravenously over 30 minutes every 3 weeks.
`
`Non-Small Cell Lung Cancer
`2.2
`The recommended dose of ABRAXANE is 100 mg/m2 administered as an intravenous infusion over 30 minutes on Days 1, 8, and
`15 of each 21-day cycle. Administer carboplatin on Day 1 of each 21 day cycle immediately after ABRAXANE [see Clinical Studies
`(14.2)].
`
`Adenocarcinoma of the Pancreas
`2.3
`The recommended dose of ABRAXANE is 125 mg/m2 administered as an intravenous infusion over 30-40 minutes on Days 1, 8 and
`15 of each 28-day cycle. Administer gemcitabine immediately after ABRAXANE on Days 1, 8 and 15 of each 28-day cycle [see
`Clinical Studies (14.3)].
`
`Dosage in Patients with Hepatic Impairment
`2.4
`For patients with mild hepatic impairment (total bilirubin greater than ULN and less than or equal to 1.5 x ULN and aspartate
`aminotransferase [AST] less than or equal to 10 x ULN), no dose adjustments are required, regardless of indication.
`
`Do not administer ABRAXANE to patients with metastatic adenocarcinoma of the pancreas who have moderate to severe hepatic
`impairment.
`
`Do not administer ABRAXANE to patients with total bilirubin greater than 5 x ULN or AST greater than 10 x ULN regardless of
`indication as these patients have not been studied.
`
`Recommendations for dosage adjustment for the first course of therapy are shown in Table 1.
`
`
`
`Reference ID: 3793488
`
`3
`
`
`
`Table 1: Recommendations for Starting Dose in Patients with Hepatic Impairment
`SGOT (AST)
`Bilirubin
`Levels
`Levels
`
`
`
`
`
`ABRAXANE Dosea
`
`
`
`NSCLC c
`100 mg/m2
`80 mg/m2 b
`80 mg/m2 b
`not recommended
`
`Pancreatic c
`Adenocarcinoma
`125 mg/m2
`not recommended
`not recommended
`not recommended
`
`
`
`
`
`MBC
`260 mg/m2
`> ULN to ≤ 1. 5 x ULN
`AND
`< 10 x ULN
`Mild
`200 mg/m2 b
`> 1.5 to ≤ 3 x ULN
`AND
`< 10 x ULN
`Moderate
`200 mg/m2 b
`> 3 to ≤ 5 x ULN
`AND
`< 10 x ULN
`Severe
`not recommended
`> 5 x ULN
`OR
`> 10 x ULN
`
`MBC = Metastatic Breast Cancer; NSCLC = Non-Small Cell Lung Cancer.
`a Dosage recommendations are for the first course of therapy. The need for further dose adjustments in subsequent courses
`should be based on individual tolerance.
`b A dose increase to 260 mg/m2 for patients with metastatic breast cancer or 100 mg/m2 for patients with non-small cell lung cancer
`in subsequent courses should be considered if the patient tolerates the reduced dose for two cycles.
`c Patients with bilirubin levels above the upper limit of normal were excluded from clinical trials for pancreatic or lung cancer.
`
`2.5
`
`Metastatic Breast Cancer
`Patients who experience severe neutropenia (neutrophils less than 500 cells/mm3 for a week or longer) or severe sensory
`neuropathy during ABRAXANE therapy should have dosage reduced to 220 mg/m2 for subsequent courses of ABRAXANE. For
`recurrence of severe neutropenia or severe sensory neuropathy, additional dose reduction should be made to 180 mg/m2. For
`Grade 3 sensory neuropathy hold treatment until resolution to Grade 1 or 2, followed by a dose reduction for all subsequent courses
`of ABRAXANE [see Contraindications (4), Warnings and Precautions (5.1, 5.2) and Adverse Reactions (6.1)].
`
`Non-Small Cell Lung Cancer
`• Do not administer ABRAXANE on Day 1 of a cycle until absolute neutrophil count (ANC) is at least 1500 cells/mm3 and platelet
`count is at least 100,000 cells/mm3 [see Contraindications (4), Warnings and Precautions (5.1) and Adverse Reactions (6.2)].
`• In patients who develop severe neutropenia or thrombocytopenia withhold treatment until counts recover to an absolute neutrophil
`count of at least 1500 cells/mm3 and platelet count of at least 100,000 cells/mm3 on Day 1 or to an absolute neutrophil count of at
`least 500 cells/mm3 and platelet count of at least 50,000 cells/mm3 on Days 8 or 15 of the cycle. Upon resumption of dosing,
`permanently reduce ABRAXANE and carboplatin doses as outlined in Table 2.
`• Withhold ABRAXANE for Grade 3-4 peripheral neuropathy. Resume ABRAXANE and carboplatin at reduced doses (see Table 2)
`when peripheral neuropathy improves to Grade 1 or completely resolves [see Warnings and Precautions (5.2) and Adverse
`Reactions (6.2)].
`
`Dose Reduction/Discontinuation Recommendations
`
`
`
`Table 2: Permanent Dose Reductions for Hematologic and Neurologic Adverse Drug Reactions in NSCLC
`
`Adverse Drug Reaction
`
`Occurrence
`
`Weekly
`ABRAXANE Dose
`(mg/m2)
`
`Every 3-Week
`Carboplatin Dose
`(AUC mg•min/mL)
`
`Neutropenic Fever (ANC less than 500/mm3 with fever
`>38°C)
`
`OR
`Delay of next cycle by more than 7 days for ANC less than
`1500/mm3
`
`OR
`ANC less than 500/mm3 for more than 7 days
`
`Platelet count less than 50,000/mm3
`
`Severe sensory Neuropathy – Grade 3 or 4
`
`
`
`First
`
`Second
`
`Third
`
`First
`
`Second
`
`First
`
`Second
`
`Third
`
`75
`
`50
`
`75
`
`75
`
`50
`
`4.5
`
`3
`
`Discontinue Treatment
`
`4.5
`
`Discontinue Treatment
`
`4.5
`
`3
`
`Discontinue Treatment
`
`
`Reference ID: 3793488
`
`4
`
`
`
`Adenocarcinoma of the Pancreas
`Dose level reductions for patients with adenocarcinoma of the pancreas, as referenced in Tables 4 and 5, are provided in Table 3.
`
`
`Table 3: Dose Level Reductions for Patients with Adenocarcinoma of the Pancreas
`
`Dose Level
`Full dose
`1st dose reduction
`2nd dose reduction
`If additional dose reduction required
`
`ABRAXANE (mg/m2)
`125
`100
`75
`Discontinue
`
`Gemcitabine (mg/m2)
`1000
`800
`600
`Discontinue
`
`
`Recommended dose modifications for neutropenia and thrombocytopenia for patients with adenocarcinoma of the pancreas are
`provided in Table 4.
`
`
`Table 4: Dose Recommendation and Modifications for Neutropenia and/or Thrombocytopenia at the Start of a Cycle or
`within a Cycle for Patients with Adenocarcinoma of the Pancreas
`
`ANC (cells/mm3)
`
`
`
`Platelet count (cells/mm3)
`
`ABRAXANE / Gemcitabine
`
`Cycle
`Day
`Day 1
`Day 8
`
`
`< 1500
`500 to < 1000
`< 500
`
`OR
`OR
`OR
`
`< 100,000
`50,000 to < 75,000
`< 50,000
`
`Day 15: If Day 8 doses were reduced or given without modification:
`
`
`
`OR
`OR
`
`50,000 to < 75,000
`< 50,000
`
`500 to < 1000
`< 500
`
`Day 15: If Day 8 doses were withheld:
`
`Delay doses until recovery
`Reduce 1 dose level
`Withhold doses
`
`Reduce 1 dose level from Day 8
`Withhold doses
`
`Reduce 1 dose level from Day 1
`Reduce 2 dose levels from Day 1
`Withhold doses
`
`OR
`OR
`OR
`
`≥ 75,000
`50,000 to < 75,000
`< 50,000
`
`
`≥ 1000
`
`500 to < 1000
`
`< 500
`ANC = Absolute Neutrophil Count
`
`Recommended dose modifications for other adverse drug reactions in patients with adenocarcinoma of the pancreas are provided in
`Table 5.
`
`
`Table 5: Dose Modifications for Other Adverse Drug Reactions in Patients with Adenocarcinoma of the Pancreas
`
`Adverse Drug Reaction
`Febrile Neutropenia:
`Grade 3 or 4
`Peripheral Neuropathy:
`Grade 3 or 4
`Cutaneous Toxicity:
`Grade 2 or 3
`Gastrointestinal Toxicity:
`Grade 3 mucositis or diarrhea
`
`ABRAXANE
`
`Gemcitabine
`
`Withhold until fever resolves and ANC ≥ 1500; resume at next lower dose level
`
`Withhold until improves to ≤ Grade 1;
`resume at next lower dose level
`
`No dose reduction
`
`Reduce to next lower dose level; discontinue treatment if toxicity persists
`
`Withhold until improves to ≤ Grade 1;
`resume at next lower dose level
`
`
`Preparation and Administration Precautions
`2.6
`ABRAXANE is a cytotoxic drug and, as with other potentially toxic paclitaxel compounds, caution should be exercised in handling
`ABRAXANE. The use of gloves is recommended. If ABRAXANE (lyophilized cake or reconstituted suspension) contacts the skin,
`wash the skin immediately and thoroughly with soap and water. Following topical exposure to paclitaxel, events may include
`tingling, burning and redness. If ABRAXANE contacts mucous membranes, the membranes should be flushed thoroughly with
`water.
`
`
`
`Reference ID: 3793488
`
`5
`
`
`
`Given the possibility of extravasation, it is advisable to closely monitor the infusion site for possible infiltration during drug
`administration. Limiting the infusion of ABRAXANE to 30 minutes, as directed, reduces the likelihood of infusion-related reactions
`[see Adverse Reactions (6.4)].
`
`Premedication to prevent hypersensitivity reactions is generally not needed prior to the administration of ABRAXANE.
`Premedication may be needed in patients who have had prior hypersensitivity reactions to ABRAXANE. Patients who experience a
`severe hypersensitivity reaction to ABRAXANE should not be re-challenged with this drug [see Warnings and Precautions (5.5)].
`
`Preparation for Intravenous Administration
`2.7
`ABRAXANE is supplied as a sterile lyophilized powder for reconstitution before use. AVOID ERRORS, READ ENTIRE
`PREPARATION INSTRUCTIONS PRIOR TO RECONSTITUTION.
`
`
`1.
`2.
`
`Aseptically, reconstitute each vial by injecting 20 mL of 0.9% Sodium Chloride Injection, USP.
`Slowly inject the 20 mL of 0.9% Sodium Chloride Injection, USP, over a minimum of 1 minute, using the
`sterile syringe to direct the solution flow onto the INSIDE WALL OF THE VIAL.
`
`
`DO NOT INJECT the 0.9% Sodium Chloride Injection, USP, directly onto the lyophilized cake as this will
`result in foaming.
`Once the injection is complete, allow the vial to sit for a minimum of 5 minutes to ensure proper wetting of
`the lyophilized cake/powder.
`Gently swirl and/or invert the vial slowly for at least 2 minutes until complete dissolution of any cake/powder
`occurs. Avoid generation of foam.
`If foaming or clumping occurs, stand solution for at least 15 minutes until foam subsides.
`
`3.
`
`4.
`
`5.
`
`6.
`
`
`Each mL of the reconstituted formulation will contain 5 mg/mL paclitaxel.
`
`The reconstituted suspension should be milky and homogenous without visible particulates. If particulates or settling are visible, the
`vial should be gently inverted again to ensure complete resuspension prior to use. Discard the reconstituted suspension if
`precipitates are observed. Discard any unused portion.
`
`Calculate the exact total dosing volume of 5 mg/mL suspension required for the patient and slowly withdraw the dosing volume of
`the reconstituted suspension from the vial(s) into a syringe: Dosing volume (mL)=Total dose (mg)/5 (mg/mL).
`
`Inject the appropriate amount of reconstituted ABRAXANE into an empty, sterile intravenous bag [plasticized polyvinyl chloride
`(PVC) containers, PVC or non-PVC type intravenous bag]. The use of specialized DEHP-free solution containers or administration
`sets is not necessary to prepare or administer ABRAXANE infusions. The use of medical devices containing silicone oil as a
`lubricant (ie, syringes and intravenous bags) to reconstitute and administer ABRAXANE may result in the formation of proteinaceous
`strands.
`
`Visually inspect the reconstituted ABRAXANE suspension in the intravenous bag prior to administration. Discard the reconstituted
`suspension if proteinaceous strands, particulate matter or discoloration are observed.
`
`Stability
`2.8
`Unopened vials of ABRAXANE are stable until the date indicated on the package when stored between 20ºC to 25ºC (68ºF to 77ºF)
`in the original package. Neither freezing nor refrigeration adversely affects the stability of the product.
`
`Stability of Reconstituted Suspension in the Vial
`Reconstituted ABRAXANE in the vial should be used immediately, but may be refrigerated at 2ºC to 8ºC (36ºF to 46ºF) for a
`maximum of 24 hours if necessary. If not used immediately, each vial of reconstituted suspension should be replaced in the original
`carton to protect it from bright light. Discard any unused portion.
`
`Stability of Reconstituted Suspension in the Infusion Bag
`The suspension for infusion when prepared as recommended in an infusion bag should be used immediately, but may be
`refrigerated at 2°C to 8°C (36°F to 46°F) and protected from bright light for a maximum of 24 hours.
`
`The total combined refrigerated storage time of reconstituted ABRAXANE in the vial and in the infusion bag is 24 hours. This may
`be followed by storage in the infusion bag at ambient temperature (approximately 25°C) and lighting conditions for a maximum of
`4 hours.
`
`
`
`Reference ID: 3793488
`
`6
`
`
`
`Discard any unused portion.
`
` 3
`
`DOSAGE FORMS AND STRENGTHS
`
`For injectable suspension: lyophilized powder containing 100 mg of paclitaxel formulated as albumin-bound particles in single-use
`vial for reconstitution.
`
` 4
`
`
`
`CONTRAINDICATIONS
`• ABRAXANE should not be used in patients who have baseline neutrophil counts of < 1,500 cells/mm3.
`• Patients who experience a severe hypersensitivity reaction to ABRAXANE should not be rechallenged with the drug.
`
` 5
`
` WARNINGS AND PRECAUTIONS
`
`
`Hematologic Effects
`5.1
`Bone marrow suppression (primarily neutropenia) is dose-dependent and a dose-limiting toxicity of ABRAXANE. In clinical studies,
`Grade 3-4 neutropenia occurred in 34% of patients with metastatic breast cancer (MBC), 47% of patients with non-small cell lung
`cancer (NSCLC), and 38% of patients with pancreatic cancer.
`
`Monitor for myelotoxicity by performing complete blood cell counts frequently, including prior to dosing on Day 1 (for MBC) and
`Days 1, 8, and 15 (for NSCLC and for pancreatic cancer). Do not administer ABRAXANE to patients with baseline absolute
`neutrophil counts (ANC) of less than 1,500 cells/mm3. In the case of severe neutropenia (<500 cells/mm3 for seven days or more)
`during a course of ABRAXANE therapy, reduce the dose of ABRAXANE in subsequent courses in patients with either MBC or
`NSCLC.
`
`In patients with MBC, resume treatment with every-3-week cycles of ABRAXANE after ANC recovers to a level >1,500 cells/mm3
`and platelets recover to a level >100,000 cells/mm3.
`
`In patients with NSCLC, resume treatment if recommended (see Dosage and Administration, Table 2) at permanently reduced
`doses for both weekly ABRAXANE and every-3-week carboplatin after ANC recovers to at least 1500 cells/mm3 and platelet count
`of at least 100,000 cells/mm3 on Day 1 or to an ANC of at least 500 cells/mm3 and platelet count of at least 50,000 cells/mm3 on
`Days 8 or 15 of the cycle [see Dosage and Administration (2.5)].
`
`In patients with adenocarcinoma of the pancreas, withhold ABRAXANE and gemcitabine if the ANC is less than 500 cells/mm3 or
`platelets are less than 50,000 cells/mm3 and delay initiation of the next cycle if the ANC is less than 1500 cells/mm3 or platelet count
`is less than 100,000 cells/mm3 on Day 1 of the cycle. Resume treatment with appropriate dose reduction if recommended [see
`Dosage and Administration (2.5)].
`
`Nervous System
`5.2
`Sensory neuropathy is dose- and schedule-dependent [see Adverse Reactions (6.1, 6.2, 6.3)]. The occurrence of Grade 1 or 2
`sensory neuropathy does not generally require dose modification. If ≥ Grade 3 sensory neuropathy develops, withhold ABRAXANE
`treatment until resolution to Grade 1 or 2 for metastatic breast cancer or until resolution to ≤ Grade 1 for NSCLC and pancreatic
`cancer followed by a dose reduction for all subsequent courses of ABRAXANE [see Dosage and Administration (2.5)].
`
`5.3 Sepsis
`Sepsis occurred in 5% of patients with or without neutropenia who received ABRAXANE in combination with gemcitabine. Biliary
`obstruction or presence of biliary stent were risk factors for severe or fatal sepsis. If a patient becomes febrile (regardless of ANC)
`initiate treatment with broad spectrum antibiotics. For febrile neutropenia, interrupt ABRAXANE and gemcitabine until fever resolves
`and ANC ≥ 1500, then resume treatment at reduced dose levels [see Dosage and Administration (2.5)].
`
`Pneumonitis
`5.4
`Pneumonitis, including some cases that were fatal, occurred in 4% of patients receiving ABRAXANE in combination with
`gemcitabine. Monitor patients for signs and symptoms of pneumonitis and interrupt ABRAXANE and gemcitabine during evaluation
`of suspected pneumonitis. After ruling out infectious etiology and upon making a diagnosis of pneumonitis, permanently discontinue
`treatment with ABRAXANE and gemcitabine.
`
`Hypersensitivity
`5.5
`Severe and sometimes fatal hypersensitivity reactions, including anaphylactic reactions, have been reported. Patients who
`experience a severe hypersensitivity reaction to ABRAXANE should not be rechallenged with this drug.
`
`
`
`Reference ID: 3793488
`
`7
`
`
`
`Hepatic Impairment
`5.6
`Because the exposure and toxicity of paclitaxel can be increased with hepatic impairment, administration of ABRAXANE in patients
`with hepatic impairment should be performed with caution. Patients with hepatic impairment may be at increased risk of toxicity,
`particularly from myelosuppression; such patients should be closely monitored for development of profound myelosuppression.
`ABRAXANE is not recommended in patients who have total bilirubin >5 x ULN or AST >10 x ULN. In addition, ABRAXANE is not
`recommended in patients with metastatic adenocarcinoma of the pancreas who have moderate to severe hepatic impairment (total
`bilirubin >1.5 x ULN and AST ≤10 x ULN). The starting dose should be reduced for patients with moderate or severe hepatic
`impairment [see Dosage and Administration (2.4), Use in Specific Populations (8.6) and Clinical Pharmacology (12.3)].
`
`Albumin (Human)
`5.7
`ABRAXANE contains albumin (human), a derivative of human blood. Based on effective donor screening and product manufacturing
`processes, it carries a remote risk for transmission of viral diseases. A theoretical risk for transmission of Creutzfeldt-Jakob Disease
`(CJD) also is considered extremely remote. No cases of transmission of viral diseases or CJD have ever been identified for
`albumin.
`
`Use in Pregnancy
`5.8
`ABRAXANE can cause fetal harm when administered to a pregnant woman. Administration of paclitaxel formulated as
`albumin-bound particles to rats during pregnancy at doses lower than the maximum recommended human dose, based on body
`surface area, caused embryo-fetal toxicities, including intrauterine mortality, increased resorptions, reduced numbers of live fetuses,
`and malformations.
`
`There are no adequate and well-controlled studies in pregnant women receiving ABRAXANE. If this drug is used during pregnancy,
`or if the patient becomes pregnant while receiving this drug, the patient should be apprised of the potential hazard to the fetus.
`Women of childbearing potential should be advised to avoid becoming pregnant while receiving ABRAXANE [see Use in Specific
`Populations (8.1)].
`
`Use in Men
`5.9
`Men should be advised not to father a child while receiving ABRAXANE [see Nonclinical Toxicology (13.1)].
`
` 6
`
`ADVERSE REACTIONS
`
`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.
`
`The most common adverse reactions (≥ 20%) with single-agent use of ABRAXANE in metastatic breast cancer are alopecia,
`neutropenia, sensory neuropathy, abnormal ECG, fatigue/asthenia, myalgia/arthralgia, AST elevation, alkaline phosphatase
`elevation, anemia, nausea, infections, and diarrhea [see Adverse Reactions (6.1)].
`
`The most common adverse reactions (≥ 20%) of ABRAXANE in combination with carboplatin for non-small cell lung cancer are
`anemia, neutropenia, thrombocytopenia, alopecia, peripheral neuropathy, nausea, and fatigue [see Adverse Reactions (6.2)]. The
`most common serious adverse reactions of ABRAXANE in combination with carboplatin for non-small cell lung cancer are anemia
`(4%) and pneumonia (3%). The most common adverse reactions resulting in permanent discontinuation of ABRAXANE are
`neutropenia (3%), thrombocytopenia (3%), and peripheral neuropathy (1%). The most common adverse reactions resulting in dose
`reduction of ABRAXANE are neutropenia (24%), thrombocytopenia (13%), and anemia (6%). The most common adverse reactions
`leading to withholding or delay in ABRAXANE dosing are neutropenia (41%), thrombocytopenia (30%), and anemia (16%).
`
`In a randomized open-label trial of ABRAXANE in combination with gemcitabine for pancreatic adenocarcinoma [see Clinical
`Studies (14.3)], the most common (≥ 20%) selected (with a ≥ 5% higher incidence) adverse reactions of ABRAXANE are
`neutropenia, fatigue, peripheral neuropathy, nausea, alopecia, peripheral edema, diarrhea, pyrexia, vomiting, decreased appetite,
`rash, and dehydration. The most common serious adverse reactions of ABRAXANE (with a ≥ 1% higher incidence) are pyrexia
`(6%), dehydration (5%), pneumonia (4%) and vomiting (4%). The most common adverse reactions resulting in permanent
`discontinuation of ABRAXANE are peripheral neuropathy (8%), fatigue (4%) and thrombocytopenia (2%). The most common
`adverse reactions resulting in dose reduction of ABRAXANE are neutropenia (10%) and peripheral neuropathy (6%). The most
`common adverse reactions leading to withholding or delay in ABRAXANE dosing are neutropenia (16%), thrombocytopenia (12%),
`fatigue (8%), peripheral neuropathy (15%), anemia (5%) and diarrhea (5%).
`
`Clinical Trials Experience in Metastatic Breast Cancer
`6.1
`Table 6 shows the frequency of important adverse events in the randomized comparative trial for the patients who received either
`single-agent ABRAXANE or paclitaxel injection for the treatment of metastatic breast cancer.
`
`
`
`Reference ID: 3793488
`
`8
`
`
`
`Table 6: Frequencya of Important Treatment Emergent Adverse Events in the Randomized Metastatic Breast
`Cancer Study on an Every-3-Weeks Schedule
`
`Percent of Patients
`ABRAXANE
`Paclitaxel Injection
`260 mg/m2 over 30 min
`175 mg/m2 over 3 hb
`(n=229)
`(n=225)
`
`
`
`
`80
`82
`9
`22
`
` 3
`
`
`<1
`
`25
`<1
`20
`1
`<1
`2
`
`12
`2
`
`
`<1
`5
`4
`
`52
`30
`
`6
`9
`
`56
`2
`
`49
`4
`
`39
`3
`
`8
`<1
`
`
`22
`<1
`
`10
`1
`
`15
`1
`
`6
`0
`94
`
`7
`31
`32
`
` 2
`
`
`<1
`
`33
`1
`24
`2
`<1
`2
`
`4
`0
`
`
`<1
`5
`3
`
`60
`35
`
`7
`12
`
`71
`10
`
`44
`8
`
`47
`8
`
`10
`0
`
`
`30
`3
`
`18
`4
`
`27
`<1
`
`7
`<1
`90
`
`7
`36
`39
`
`
`
`
`
`
`Bone Marrow
` Neutropenia
` < 2.0 x 109/L
` < 0.5 x 109/L
` Thrombocytopenia
` < 100 x 109/L
` < 50 x 109/L
` Anemia
` < 11 g/dL
` < 8 g/dL
` Infections
` Febrile Neutropenia
` Neutropenic Sepsis
` Bleeding
`Hypersensitivity Reactionc
` All
` Severed
`Cardiovascular
` Vital Sign Changes During Administration
` Bradycardia
` Hypotension
` Severe Cardiovascular Eventsd
`Abnormal ECG
` All Patients
` Patients with Normal Baseline
`Respiratory
` Cough
` Dyspnea
`Sensory Neuropathy
` Any Symptoms
` Severe Symptomsd
`Myalgia / Arthralgia
` Any Symptoms
` Severe Symptomsd
`Asthenia
` Any Symptoms
` Severe Symptomsd
`Fluid Retention/Edema
` Any Symptoms
` Severe Symptomsd
`Gastrointestinal
` Nausea
`