DOSAGE & ADMINISTRATION SECTION.

2 DOSAGE AND ADMINISTRATION. oWith lenalidomide and dexamethasone: 10 mg/kg administered intravenously every week for the first two cycles and every weeks thereafter until disease progression or unacceptable toxicity. (2.1)oWith pomalidomide and dexamethasone: 10 mg/kg administered intravenously every week for the first two cycles and 20 mg/kg every weeks thereafter until disease progression or unacceptable toxicity. (2.2)oPremedicate with dexamethasone, diphenhydramine, ranitidine and acetaminophen. (2.3). oWith lenalidomide and dexamethasone: 10 mg/kg administered intravenously every week for the first two cycles and every weeks thereafter until disease progression or unacceptable toxicity. (2.1). oWith pomalidomide and dexamethasone: 10 mg/kg administered intravenously every week for the first two cycles and 20 mg/kg every weeks thereafter until disease progression or unacceptable toxicity. (2.2). oPremedicate with dexamethasone, diphenhydramine, ranitidine and acetaminophen. (2.3). 2.1 Recommended Dosing when EMPLICITI Is Used in Combination with Lenalidomide and Dexamethasone. The recommended dosage of EMPLICITI is 10 mg/kg administered intravenously every week for the first two cycles (28-day cycle) and every weeks thereafter in conjunction with the recommended dosing of lenalidomide and low-dose dexamethasone as described below. Continue treatment until disease progression or unacceptable toxicity.Refer to the dexamethasone and lenalidomide prescribing information for additional information.Administer premedications before each dose of EMPLICITI [see Dosage and Administration (2.3) and Warnings and Precautions (5.1) ].Administer dexamethasone as follows:oOn days that EMPLICITI is administered, give dexamethasone 28 mg orally between and 24 hours before EMPLICITI plus mg intravenously between 45 and 90 minutes before EMPLICITI.oOn days that EMPLICITI is not administered but dose of dexamethasone is scheduled (Days and 22 of cycle and all subsequent cycles), give 40 mg orally.The recommended dosing is presented in Table 1.Table 1: Recommended Dosing Schedule of EMPLICITI in Combination with Lenalidomide and DexamethasoneCycle28-Day Cycles and 228-Day Cycles 3+ Premedicate with the following 45 to 90 minutes prior to EMPLICITI infusion: mg intravenous dexamethasone, H1 blocker: diphenhydramine (25 to 50 mg orally or intravenously) or equivalent; H2 blocker: ranitidine (50 mg intravenously) or equivalent; acetaminophen (650 to 1000 mg orally). Oral dexamethasone (28 mg) taken between and 24 hours before EMPLICITI infusion. Intravenous dexamethasone 45-90 minutes before EMPLICITI infusion.Day of Cycle181522181522PremedicationEMPLICITI (mg/kg) intravenously101010101010Lenalidomide (25 mg) orallyDays 1-21Days 1-21Dexamethasone+ (mg) orally2828282828402840Dexamethasone (mg) intravenously888888Day of Cycle181522181522. oOn days that EMPLICITI is administered, give dexamethasone 28 mg orally between and 24 hours before EMPLICITI plus mg intravenously between 45 and 90 minutes before EMPLICITI.. oOn days that EMPLICITI is not administered but dose of dexamethasone is scheduled (Days and 22 of cycle and all subsequent cycles), give 40 mg orally.. 2.2 Recommended Dosing when EMPLICITI Is Used in Combination with Pomalidomide and Dexamethasone The recommended dosage of EMPLICITI is 10 mg/kg administered intravenously every week for the first two cycles (28-day cycle). Starting at cycle (28-day cycle), administer EMPLICITI 20 mg/kg intravenously every weeks. Administer EMPLICITI in conjunction with pomalidomide and low-dose dexamethasone as described below (Table 2). Continue treatment until disease progression or unacceptable toxicity.Refer to the dexamethasone and pomalidomide prescribing information for additional information.Administer premedications before each dose of EMPLICITI [see Dosage and Administration (2.3)andWarnings and Precautions (5.1)].Administer dexamethasone as follows:oOn days that EMPLICITI is administered, for patients 75 years or younger give dexamethasone 28 mg orally between and 24 hours before EMPLICITI plus mg intravenously between 45 and 90 minutes before EMPLICITI and for patients older than 75 years give dexamethasone mg orally between and 24 hours before EMPLICITI plus mg intravenously between 45 and 90 minutes before EMPLICITI.oOn days that EMPLICITI is not administered but dose of dexamethasone is scheduled (Days 8, 15 and 22 of cycle and all subsequent cycles), give 40 mg orally to patients 75 years or younger and 20 mg orally to patients older than 75 years.The recommended dosing is presented in Table 2.Table 2: Recommended Dosing Schedule of EMPLICITI in Combination with Pomalidomide and DexamethasoneCycle28-Day Cycles and 228-Day Cycles 3+ Premedicate with the following 45 to 90 minutes prior to EMPLICITI infusion: mg intravenous dexamethasone, H1 blocker: diphenhydramine (25 to 50 mg orally or intravenously) or equivalent; H2 blocker: ranitidine (50 mg intravenously) or equivalent; acetaminophen (650 to 1000 mg orally).+ Oral dexamethasone taken between and 24 hours before EMPLICITI infusion. Intravenous dexamethasone 45-90 minutes before EMPLICITI infusion.Day of Cycle181522181522PremedicationEMPLICITI (mg/kg) intravenously1010101020Pomalidomide (4 mg) orallyDays 1-21Days 1-21Dexamethasone+ (mg) orally <=75 years old2828282828404040Dexamethasone+ (mg) orally >75 years old88888202020Dexamethasone (mg) intravenously88888 oOn days that EMPLICITI is administered, for patients 75 years or younger give dexamethasone 28 mg orally between and 24 hours before EMPLICITI plus mg intravenously between 45 and 90 minutes before EMPLICITI and for patients older than 75 years give dexamethasone mg orally between and 24 hours before EMPLICITI plus mg intravenously between 45 and 90 minutes before EMPLICITI.. oOn days that EMPLICITI is not administered but dose of dexamethasone is scheduled (Days 8, 15 and 22 of cycle and all subsequent cycles), give 40 mg orally to patients 75 years or younger and 20 mg orally to patients older than 75 years.. 2.3 Premedication. Dexamethasone. When EMPLICITI is used in combination with lenalidomide or pomalidomide and dexamethasone, divide dexamethasone into an oral and intravenous dose and administer as shown in Table and Table [see Dosage and Administration (2.1, 2.2) ].. Other Medications. In addition to dexamethasone, complete administration of the following medications 45 to 90 minutes prior to EMPLICITI infusion:oH1 blocker: diphenhydramine (25 to 50 mg orally or intravenously) or equivalent H1 blocker.oH2 blocker: ranitidine (50 mg intravenously or 150 mg orally) or equivalent H2 blocker.oAcetaminophen (650 to 1000 mg orally).. oH1 blocker: diphenhydramine (25 to 50 mg orally or intravenously) or equivalent H1 blocker.. oH2 blocker: ranitidine (50 mg intravenously or 150 mg orally) or equivalent H2 blocker.. oAcetaminophen (650 to 1000 mg orally).. 2.4 Dose Modifications. If the dose of one drug in the regimen is delayed, interrupted, or discontinued, the treatment with the other drugs may continue as scheduled. However, if dexamethasone is delayed or discontinued, base the decision whether to administer EMPLICITI on clinical judgment (i.e., risk of hypersensitivity).If Grade or higher infusion reaction occurs during EMPLICITI administration, interrupt the infusion and institute appropriate medical and supportive measures. Upon resolution to Grade or lower, restart EMPLICITI at 0.5 mL per minute and gradually increase at rate of 0.5 mL per minute every 30 minutes as tolerated to the rate at which the infusion reaction occurred. Resume the escalation regimen if there is no recurrence of the infusion reaction (see Table and Table 4).In patients who experience an infusion reaction, monitor vital signs every 30 minutes for hours after the end of the EMPLICITI infusion. If the infusion reaction recurs, stop the EMPLICITI infusion and do not restart on that day [see Warnings and Precautions (5.1) ]. Severe infusion reactions may require permanent discontinuation of EMPLICITI therapy and emergency treatment.Dose delays and modifications for dexamethasone, pomalidomide and lenalidomide should be performed as recommended in their Prescribing Information.. 2.5 Administration Administer the entire EMPLICITI infusion with an infusion set and sterile, nonpyrogenic, low-protein-binding filter (with pore size of 0.2 to 1.2 micrometer) using an automated infusion pump.Initiate EMPLICITI infusion at rate of 0.5 mL per minute for 10 mg/kg dose. The infusion rate may be increased in stepwise fashion as described in Table if no infusion reactions develop. The maximum infusion rate should not exceed mL per minute.Table 3: Infusion Rate for EMPLICITI 10 mg/kgCycle 1, Dose 1Cycle 1, Dose 2Cycle 1, Dose and and All Subsequent CyclesTime IntervalRateTime IntervalRateRate0-30 min0.5 mL/min0-30 min3 mL/min30-60 min1 mL/min30 min or more4 mL/min5 mL/min60 min or more2 mL/min--Initiate EMPLICITI infusion rate at mL per minute for 20 mg/kg dose. The infusion rate may be increased in stepwise fashion as described in Table if no infusion reactions develop. The maximum infusion rate should not exceed mL per minute.Patients who have escalated to mL/min at 10 mg/kg dose must decrease the rate to mL/min at the first infusion at 20 mg/kg.Table 4: Infusion Rate for EMPLICITI 20 mg/kgDose 1Dose and all subsequent dosesTime IntervalRateRate0-30 min3 mL/min30 min or more4 mL/min5 mL/minAdjust the infusion rate following Grade or higher infusion reaction [see Dosage and Administration (2.4)].Do not mix EMPLICITI with, or administer as an infusion with, other medicinal products. No physical or biochemical compatibility studies have been conducted to evaluate the coadministration of EMPLICITI with other agents.. 2.6 Reconstitution and Preparation Calculation of Dose. oCalculate the dose (mg) and determine the number of vials needed for the 10 mg/kg and 20 mg/kg dosage based on patient weight.oDetermine the volume of sterile water for injection (SWFI) needed for reconstitution as shown in Table 5.Table 5: Reconstitution Instructions for EMPLICITIStrengthAmount of Sterile Water for Injection, USP Required for ReconstitutionDeliverable Volume of Reconstituted EMPLICITI in the VialPostreconstitution Concentration After reconstitution, each vial contains overfill to allow for withdrawal of 12 mL (300 mg) and 16 mL (400 mg), respectively.300 mg vial13 mL12 mL25 mg/mL400 mg vial17 mL16 mL25 mg/mL. oCalculate the dose (mg) and determine the number of vials needed for the 10 mg/kg and 20 mg/kg dosage based on patient weight.. oDetermine the volume of sterile water for injection (SWFI) needed for reconstitution as shown in Table 5.. Reconstitution. oAseptically reconstitute each EMPLICITI vial with syringe of adequate size and less than or equal to 18-gauge needle (e.g., 17-gauge). slight back pressure may be experienced during administration of the Sterile Water for Injection, USP, which is considered normal.oHold the vial upright and swirl the solution by rotating the vial to dissolve the lyophilized cake. Invert the vial few times in order to dissolve any powder that may be present on top of the vial or the stopper. Avoid vigorous agitation. DO NOT SHAKE. The lyophilized powder should dissolve in less than 10 minutes.oAfter the remaining solids are completely dissolved, allow the reconstituted solution to stand for to 10 minutes. The reconstituted preparation results in colorless to slightly yellow, clear to slightly opalescent solution. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. Discard the solution if any particulate matter or discoloration is observed.. oAseptically reconstitute each EMPLICITI vial with syringe of adequate size and less than or equal to 18-gauge needle (e.g., 17-gauge). slight back pressure may be experienced during administration of the Sterile Water for Injection, USP, which is considered normal.. oHold the vial upright and swirl the solution by rotating the vial to dissolve the lyophilized cake. Invert the vial few times in order to dissolve any powder that may be present on top of the vial or the stopper. Avoid vigorous agitation. DO NOT SHAKE. The lyophilized powder should dissolve in less than 10 minutes.. oAfter the remaining solids are completely dissolved, allow the reconstituted solution to stand for to 10 minutes. The reconstituted preparation results in colorless to slightly yellow, clear to slightly opalescent solution. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. Discard the solution if any particulate matter or discoloration is observed.. Dilution. oOnce the reconstitution is completed, withdraw the necessary volume for the calculated dose from each vial, up to maximum of 16 mL from 400 mg vial and 12 mL from 300 mg vial.oFurther dilute with either 0.9% Sodium Chloride Injection, USP or 5% Dextrose Injection, USP, into an infusion bag made of polyvinyl chloride or polyolefin. The final infusion concentration should range between mg/mL and mg/mL.oThe volume of 0.9% Sodium Chloride Injection, USP or 5% Dextrose Injection, USP should be adjusted so as not to exceed mL/kg of patient weight at any given dose of EMPLICITI.Complete the EMPLICITI infusion within 24 hours of reconstitution of the EMPLICITI lyophilized powder. If not used immediately, the infusion solution may be stored under refrigeration conditions: 2oC to 8oC (36oF-46oF) and protected from light for up to 24 hours (a maximum of hours of the total 24 hours can be at room temperature, 20C to 25C [68F-77F], and room light).. oOnce the reconstitution is completed, withdraw the necessary volume for the calculated dose from each vial, up to maximum of 16 mL from 400 mg vial and 12 mL from 300 mg vial.. oFurther dilute with either 0.9% Sodium Chloride Injection, USP or 5% Dextrose Injection, USP, into an infusion bag made of polyvinyl chloride or polyolefin. The final infusion concentration should range between mg/mL and mg/mL.. oThe volume of 0.9% Sodium Chloride Injection, USP or 5% Dextrose Injection, USP should be adjusted so as not to exceed mL/kg of patient weight at any given dose of EMPLICITI.

ADVERSE REACTIONS SECTION.

6 ADVERSE REACTIONS. The following clinically significant adverse reactions are described in detail in other sections of the label:oInfusion reaction [see Warnings and Precautions (5.1) ].oInfections [see Warnings and Precautions (5.2) ].oSecond Primary Malignancies [see Warnings and Precautions (5.3) ].oHepatotoxicity [see Warnings and Precautions (5.4) ].oInterference with determination of complete response [see Warnings and Precautions (5.5) ].. oInfusion reaction [see Warnings and Precautions (5.1) ].. oInfections [see Warnings and Precautions (5.2) ].. oSecond Primary Malignancies [see Warnings and Precautions (5.3) ].. oHepatotoxicity [see Warnings and Precautions (5.4) ].. oInterference with determination of complete response [see Warnings and Precautions (5.5) ].. Most common adverse reactions (20% or higher)owith lenalidomide and dexamethasone are fatigue, diarrhea, pyrexia, constipation, cough, peripheral neuropathy, nasopharyngitis, upper respiratory tract infection, decreased appetite, pneumonia. (6.1)owith pomalidomide and dexamethasone are constipation and hyperglycemia. (6.1)To report SUSPECTED ADVERSE REACTIONS, contact Bristol-Myers Squibb at 1-800-721-5072 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. owith lenalidomide and dexamethasone are fatigue, diarrhea, pyrexia, constipation, cough, peripheral neuropathy, nasopharyngitis, upper respiratory tract infection, decreased appetite, pneumonia. (6.1). owith pomalidomide and dexamethasone are constipation and hyperglycemia. (6.1). 6.1 Clinical Trials Experience. Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.EMPLICITI in Combination with Lenalidomide and Dexamethasone [ELOQUENT-2]The safety data described in this section are based on the ELOQUENT-2 study, randomized, open-label clinical trial in patients with previously treated multiple myeloma. In ELOQUENT-2, EMPLICITI 10 mg/kg was administered with lenalidomide and dexamethasone [see Clinical Studies (14) ]. For adverse reaction evaluation, EMPLICITI combined with lenalidomide and dexamethasone was compared with lenalidomide and dexamethasone alone.The mean age of the population was 66 years and 57% of patients were 65 years of age or older. Sixty percent (60%) of the population were male, 84% were white, 10% were Asian, and 4% were black. The Eastern Cooperative Oncology Group (ECOG) performance status was in 47%, in 44%, and in 9% of patients.These data reflect exposure of 318 patients to EMPLICITI and 317 to control with median number of cycles of 19 for EMPLICITI and 14 for control.Serious adverse reactions were reported in 65% of patients treated on the EMPLICITI arm and 57% for patients treated on the control arm. The most frequent serious adverse reactions in the EMPLICITI arm compared to the control arm were: pneumonia (15% vs. 11%), pyrexia (7% vs. 5%), respiratory tract infection (3.1% vs. 1.3%), anemia (2.8% vs. 1.9%), pulmonary embolism (3.1% vs. 2.5%), and acute renal failure (2.5% vs. 1.9%).The proportion of patients who discontinued any component of the treatment regimen due to adverse reactions as listed below was similar for both treatment arms; 6.0% for patients treated on the EMPLICITI arm and 6.3% for patients treated on the control.Adverse reactions occurring at frequency of 10% or higher in the EMPLICITI arm and 5% or higher than the lenalidomide and dexamethasone arm for the randomized trial in multiple myeloma are presented in Table 6.Table 6: ELOQUENT-2: Adverse Reactions with 10% or Higher Incidence for EMPLICITI-Treated Patients and 5% or Higher Incidence than Lenalidomide and Dexamethasone-Treated Patients [All Grades]EMPLICITI Lenalidomide and DexamethasoneN=318Lenalidomide and Dexamethasone N=317Primary TermAll GradesGrade 3/4All GradesGrade 3/4 The term fatigue is grouping of the following terms: fatigue and asthenia. The term cough is grouping of the following terms: cough, productive cough, and upper airway cough. The term peripheral neuropathy is grouping of the following terms: peripheral neuropathy, axonal neuropathy, peripheral motor neuropathy, peripheral sensory neuropathy, and polyneuropathy. The term pneumonia is grouping of the following terms: pneumonia, atypical pneumonia, bronchopneumonia, lobar pneumonia, bacterial pneumonia, fungal pneumonia, pneumonia influenza, and pneumococcal pneumonia.Fatigue62135212Diarrhea475.0364.1Pyrexia372.5252.8Constipation361.3270.3Cough+ 340.3190Peripheral Neuropathy 273.8212.2Nasopharyngitis250190Upper Respiratory Tract Infection230.6171.3Decreased Appetite211.6131.3Pneumonia 2014149Pain in Extremities160.9100.3Headache150.380.3Vomiting140.390.9Weight Decreased141.360Lymphopenia13973.2Cataracts12662.8Oropharyngeal Pain10040Laboratory abnormalities worsening from baseline and occurring at frequency of 10% or higher in the EMPLICITI group and 5% or higher than the lenalidomide and dexamethasone group (criteria met for all Grades or Grade 3/4) for ELOQUENT-2 are presented in Table 7.Table 7: ELOQUENT-2: Laboratory Abnormalities Worsening from Baseline and with 10% or Higher Incidence for EMPLICITI-Treated Patients and 5% Higher Incidence than Lenalidomide and Dexamethasone-Treated Patients [Criteria met for All Grades or Grade 3/4]EMPLICITI Lenalidomide and DexamethasoneN=318Lenalidomide and Dexamethasone N=317Laboratory ParameterAll GradesGrade 3/4All GradesGrade 3/4Hematology Lymphopenia99779849 Leukopenia91328826 Thrombocytopenia84197820Liver and Renal Function Tests Hypoalbuminemia733.9662.3 Elevated Alkaline Phosphatase391.3300Chemistry Hyperglycemia89178510 Hypocalcemia7811774.7 Low Bicarbonate630.4450 Hyperkalemia327221.6Vital sign abnormalities were assessed by treatment arm for the randomized trial in multiple myeloma and are presented in Table 8. Percentages are based on patients who had at least one vital sign abnormality any time during the course of study.Table 8: ELOQUENT-2 Vital Sign AbnormalitiesEMPLICITI Lenalidomide and DexamethasoneN=318Lenalidomide and Dexamethasone N=317Vital Sign Parameter%%Systolic Blood Pressure >=160 mmHg3321Diastolic Blood Pressure >=100 mmHg1712Systolic Blood Pressure <90 mmHg298Heart Rate >=100 bpm4830Heart Rate <60 bpm6631EMPLICITI in Combination with Pomalidomide and Dexamethasone [ELOQUENT-3]The safety data described in this section are based on ELOQUENT-3, randomized, open-label clinical trial in patients with previously treated multiple myeloma. In ELOQUENT-3, EMPLICITI 10 mg/kg and 20 mg/kg was administered with pomalidomide and dexamethasone [see Clinical Studies (14) ]. For adverse reaction evaluation, EMPLICITI combined with pomalidomide and dexamethasone was compared with pomalidomide and dexamethasone alone.The mean age of the population was 66 years and 63% of patients were 65 years of age or older. Fifty-seven percent of the population were male, 78% were white, 20% were Asian, and none were black. The ECOG performance status was in 43%, in 46%, and in 10% of patients. These data reflect exposure of 60 patients to EMPLICITI and 55 to control with median number of cycles of for EMPLICITI and for control.Serious adverse reactions were reported in 22% of patients treated on the EMPLICITI arm and 15% for patients treated on the control arm. The most frequent serious adverse reactions in the EMPLICITI arm compared to the control arm were: pneumonia (13% vs. 11%) and respiratory tract infection (7% vs. 3.6%). The proportion of patients who discontinued any component of the treatment regimen due to adverse reactions were 5.0% of the patients in the EMPLICITI arm and 1.8% of the patients in the control arm.Adverse reactions occurring at frequency of 10% or higher in the EMPLICITI arm and 5% or higher than the pomalidomide and dexamethasone arm for the randomized trial in multiple myeloma are presented in Table 9.Table 9: ELOQUENT-3: Adverse Reactions with 10% or Higher Incidence for EMPLICITI-Treated Patients and 5% or Higher Incidence than Pomalidomide and Dexamethasone-Treated Patients [All Grades]EMPLICITI Pomalidomide and DexamethasoneN=60Pomalidomide and Dexamethasone N=55Adverse ReactionAll GradesGrade 3/4All GradesGrade 3/4 The term pneumonia is grouping of the following terms: pneumonia, atypical pneumonia, lower respiratory tract infection, pneumoccocal sepsis, pneumonia bacterial, pneumonia influenza.Constipation221.7110Hyperglycemia208157Pneumonia18101311Diarrhea18090Respiratory Tract Infection17091.8Bone Pain153.390Dyspnea153.371.8Muscle Spasms13050Edema Peripheral13070Lymphopenia1081.81.8Other clinically important adverse reactions reported in patients treated with EMPLICITI that did not meet the criteria for inclusion in Table and but occurred at frequency of 5% or greater in the EMPLICITI group and at frequency at least twice the control rate for the randomized trial in multiple myeloma are listed below:General disorders and administration site conditions: chest pain, night sweatsImmune system disorders: hypersensitivityNervous system disorders: hypoesthesiaPsychiatric disorders: mood alteredLaboratory abnormalities worsening from baseline and occurring at frequency of 10% or higher in ELOQUENT-3 in the EMPLICITI group and 5% or higher than the pomalidomide and dexamethasone group (criteria met for all Grades or Grade 3/4) for the randomized trial in multiple myeloma are presented in Table 10.Table 10: ELOQUENT-3: Laboratory Abnormalities Worsening from Baseline and with 10% or Higher Incidence for EMPLICITI-Treated Patients and 5% Higher Incidence than Pomalidomide and Dexamethasone-Treated Patients [Criteria met for All Grades or Grade 3/4]EMPLICITI Pomalidomide and DexamethasoneN=60Pomalidomide and Dexamethasone N=55Laboratory ParameterAll GradesGrade 3/4All GradesGrade 3/4Hematology Lymphopenia98709135 Leukopenia80528735 Thrombocytopenia78177320Liver and Renal Function Tests Hypoalbuminemia651.7561.8Chemistry Hypocalcemia583.3401.8 Hyperglycemia403.3251.8 Hyponatremia405180 Hypokalemia235163.6Vital sign abnormalities were assessed by treatment arm for the randomized trial in multiple myeloma and are presented in Table 11. Percentages are based on all treated patients Table 11:ELOQUENT-3: Vital Sign AbnormalitiesEMPLICITI Pomalidomide and DexamethasoneN=60Pomalidomide and Dexamethasone N=55Vital Sign Parameter%%Systolic Blood Pressure >=160 mmHg1813Diastolic Blood Pressure >=100 mmHg84.0Systolic Blood Pressure <90 mmHg77Heart Rate >=100 bpm2324Heart Rate <60 bpm4322 6.2 Immunogenicity. As with all therapeutic proteins, there is potential for immunogenicity to EMPLICITI. 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 incidence of antibodies to EMPLICITI in the studies described below with the incidences of antibodies in other studies or to other products may be misleading.Of 390 patients across four clinical studies including ELOQUENT-2 and in 53 patients in the ELOQUENT-3 trial, who were treated with EMPLICITI and evaluable for the presence of anti-product antibodies, 72 patients (18.5%) in the four clinical trials and 19 patients (36%) in the ELOQUENT-3 trial tested positive for treatment-emergent anti-product antibodies by an electrochemiluminescent (ECL) assay. In 63 (88%) of the 72 patients in the four clinical trials, anti-product antibodies occurred within the first months of the initiation of EMPLICITI treatment and resolved by to months in 49 (78%) patients. In the ELOQUENT-3 trial, in all 19 patients, anti-product antibodies occurred within the first months of the initiation of EMPLICITI treatment and were resolved by to months in 18 (95%) patients.Neutralizing antibodies post-treatment were detected in 19 of 299 patients in the four clinical trials and of 53 patients in the ELOQUENT-3 trial who were evaluable for the presence of neutralizing antibodies.

CLINICAL PHARMACOLOGY SECTION.

12 CLINICAL PHARMACOLOGY. 12.1 Mechanism of Action. Elotuzumab is humanized IgG1 monoclonal antibody that specifically targets the SLAMF7 (Signaling Lymphocytic Activation Molecule Family member 7) protein. SLAMF7 is expressed on myeloma cells independent of cytogenetic abnormalities. SLAMF7 is also expressed on Natural Killer cells, plasma cells, and at lower levels on specific immune cell subsets of differentiated cells within the hematopoietic lineage.Elotuzumab directly activates Natural Killer cells through both the SLAMF7 pathway and Fc receptors. Elotuzumab also targets SLAMF7 on myeloma cells and facilitates the interaction with Natural Killer cells to mediate the killing of myeloma cells through antibody-dependent cellular cytotoxicity (ADCC). In preclinical models, the combination of elotuzumab and lenalidomide resulted in enhanced activation of Natural Killer cells that was greater than the effects of either agent alone and increased anti-tumor activity in vitro and in vivo.. 12.2 Pharmacodynamics. Cardiac Electrophysiology. EMPLICITI does not prolong the QT interval to any clinically relevant extent when administered with lenalidomide and dexamethasone at the recommended dose or as monotherapy (at dose times the recommended dose).. 12.3 Pharmacokinetics Elotuzumab exhibits nonlinear pharmacokinetics (PK) resulting in greater than proportional increases in area under the concentration-time curve (AUC) indicative of target-mediated clearance. The administration of the recommended 10 mg/kg EMPLICITI regimen with lenalidomide and dexamethasone is predicted to result in geometric mean (CV%) steady-state trough concentrations of 194 ug/mL (52%). The administration of the recommended EMPLICITI regimen with pomalidomide and dexamethasone is predicted to result in geometric mean (CV%) steady-state trough concentrations of 124 ug/mL (59%).EliminationThe clearance of elotuzumab in combination with lenalidomide and dexamethasone decreased from geometric mean (CV%) of 17.5 (21.2%) to 5.8 (31%) mL/day/kg with an increase in dose from 0.5 (i.e., 0.05 times the recommended dosage) to 20 mg/kg (i.e., times the recommended dosage). When elotuzumab is administered with lenalidomide and dexamethasone, approximately 97% of the maximum steady-state concentration is predicted to be eliminated with geometric mean (CV%) of 82.4 (48%) days. When elotuzumab is administered with pomalidomide and dexamethasone, approximately 97% of the maximum steady-state concentration is predicted to be eliminated with geometric mean (CV%) of 78 (42%) days.. Specific Populations. Clinically significant differences were not observed in the PK of elotuzumab based on age (37 to 88 years), sex, race, baseline lactate dehydrogenase, albumin, renal impairment (creatinine clearance (CLcr) 15 to 89 mL/min), end-stage renal disease (CLcr <15 mL/min) with or without hemodialysis, mild hepatic impairment (total bilirubin <= upper limit of normal (ULN) and aspartate transaminase (AST) ULN OR total bilirubin to 1.5 times the ULN and AST any value), and coadministration with lenalidomide/dexamethasone or pomalidomide/dexamethasone. The PK of elotuzumab in patients with moderate (total bilirubin 1.5 to times the ULN and AST any value) to severe (total bilirubin 3 times the ULN and AST any value) hepatic impairment is unknown.The clearance of elotuzumab increased with increasing body weight supporting weight-based dose.

CLINICAL STUDIES SECTION.

14 CLINICAL STUDIES. ELOQUENT-2 (NCT01239797)The efficacy and safety of EMPLICITI in combination with lenalidomide and dexamethasone were evaluated in ELOQUENT-2, randomized, open-label trial in patients with multiple myeloma who had received one to three prior therapies and had documented progression following their most recent therapy.Eligible patients were randomized in 1:1 ratio to receive either EMPLICITI in combination with lenalidomide and low-dose dexamethasone or lenalidomide and low-dose dexamethasone. Treatment was administered in 4-week cycles until disease progression or unacceptable toxicity. EMPLICITI 10 mg/kg was administered intravenously each week for the first cycles and every weeks thereafter. Prior to EMPLICITI infusion, dexamethasone was administered as divided dose: an oral dose of 28 mg and an intravenous dose of mg. In the control group and on weeks without EMPLICITI, dexamethasone 40 mg was administered as single oral dose weekly. Lenalidomide 25 mg was taken orally once daily for the first weeks of each cycle. Assessment of tumor response was conducted every weeks.A total of 646 patients were randomized to receive treatment: 321 to EMPLICITI in combination with lenalidomide and low-dose dexamethasone and 325 to lenalidomide and low-dose dexamethasone.Demographics and baseline disease characteristics were balanced between treatment arms. The median age was 66 years (range, 37-91); 57% of patients were 65 years or older; 60% of patients were male; whites comprised 84% of the study population, Asians 10%, and blacks 4%. The ECOG performance status was in 47%, in 44%, and in 9% of patients, and ISS Stage was in 43%, II in 32%, and III in 21% of patients. The cytogenetic categories of del 17p and t(4;14) were present in 32% and 9% of patients, respectively. The median number of prior therapies was 2. Thirty-five percent (35%) of patients were refractory (progression during or within 60 days of last therapy) and 65% were relapsed (progression after 60 days of last therapy). Prior therapies included stem cell transplant (55%), bortezomib (70%), melphalan (65%), thalidomide (48%), and lenalidomide (6%).The efficacy of EMPLICITI was evaluated by progression-free survival (PFS) as assessed by hazard ratio, and overall response rate (ORR) as determined by blinded Independent Review Committee using the European Group for Blood and Marrow Transplantation (EBMT) response criteria. Efficacy results are shown in Table 12 and Figure 1. The median number of treatment cycles was 19 for the EMPLICITI group and 14 for the comparator arm with minimum follow-up of two years.A pre-planned final overall survival (OS) analysis was performed after at least 427 deaths occurred. The minimum follow-up was 70.6 months. The OS results at final analysis reached statistical significance. significantly longer OS was observed in patients in the E-Ld arm compared to patients in Ld arm, representing an 18% reduction in the risk of death. Efficacy results are presented in Table 12 and Figure 2.Table 12: ELOQUENT-2 Efficacy ResultsEMPLICITI Lenalidomide/DexamethasoneN=321Lenalidomide/Dexamethasone N=325PFS p-value based on the log-rank test stratified by ss2 microglobulins (<3.5 mg/L vs >=3.5 mg/L), number of prior lines of therapy (1 vs or 3), and prior immunomodulatory therapy (no vs prior thalidomide only vs other). European Group for Blood and Marrow Transplantation (EBMT) criteria. p-value based on the Cochran-Mantel-Haenszel chi-square test stratified by ss2 microglobulins (<3.5 mg/L vs >=3.5 mg/L), number of prior lines of therapy (1 vs or 3), and prior immunomodulatory therapy (no vs prior thalidomide only vs other). Complete response (CR) stringent complete response (sCR). EMPLICITIs interference with the assessment of myeloma protein with immunofixation and serum protein electrophoresis assay may interfere with correct response classification [see Drug Interactions (7)]. Hazard Ratio [95% CI]0.70 [0.57, 0.85] Stratified log-rank test p-value0.0004Median PFS in months [95% CI]19.4 [16.6, 22.2]14.9 [12.1, 17.2]ResponseOverall Response (ORR)+ (%) [95% CI]252 (78.5)[73.6, 82.9]213 (65.5)[60.1, 70.7] p-value 0.0002 Complete Response (CR sCR)+, (%)14 (4.4) 24 (7.4) Very Good Partial Response (VGPR)+ (%)91 (28.3)67 (20.6) Partial Response (PR)+ (%)147 (45.8)122 (37.5)Overall Survival Hazard Ratio [95.4% CI]0.82 [0.68, 1.00] Stratified log-rank test p-value0.0408 Median OS in months [95% CI]48.3 [40.3, 51.9]39.6 [33.3, 45.3]Figure 1: ELOQUENT-2 Progression-Free SurvivalThe 1- and 2-year rates of PFS for EMPLICITI in combination with lenalidomide and dexamethasone treatment were 68% and 41%, respectively, compared with 57% and 27%, respectively, for lenalidomide and dexamethasone treatment.Figure 2: ELOQUENT-2 Overall SurvivalELOQUENT-3 (NCT02654132)The efficacy and safety of EMPLICITI in combination with pomalidomide and dexamethasone were evaluated in ELOQUENT-3, randomized, open-label trial in patients with relapsed or refractory multiple myeloma.Eligible patients were randomized in 1:1 ratio to receive either EMPLICITI in combination with pomalidomide and low-dose dexamethasone or pomalidomide and low-dose dexamethasone. Treatment was administered in 4-week cycles until disease progression or unacceptable toxicity. EMPLICITI 10 mg/kg was administered intravenously each week for the first cycles and 20 mg/kg every weeks thereafter. Prior to EMPLICITI infusion, dexamethasone was administered. Dexamethasone was administered on day 1, 8, 15 and 22 of each cycle. On weeks with EMPLICITI infusion, dexamethasone was administered as divided dose: subjects 75 years or younger, an oral dose of 28 mg and an intravenous dose of mg, and in subjects older than 75 years an oral dose of mg and an intravenous dose of mg. On weeks without an EMPLICITI infusion and in the control group, dexamethasone was administered in subjects 75 years or younger as an oral dose of 40 mg and in subjects older than 75 years as an oral dose of 20 mg dexamethasone was administered orally. Assessment of tumor response was conducted every weeks. total of 117 patients were randomized to receive treatment: 60 to EMPLICITI in combination with pomalidomide and low-dose dexamethasone and 57 to pomalidomide and low-dose dexamethasone.Demographics and baseline disease characteristics were balanced between treatment arms. The median age was 67 years (range, 36-81); 62% of patients were 65 years or older; 57% of patients were male; whites comprised 77% of the study population, Asians 21%, and blacks 1%. The ECOG performance status was in 44%, in 46%, and in 10% of patients, and ISS Stage was in 50%, II in 38%, and III in 12% of patients. The chromosomal lab abnormalities as determined by FISH of del 17p and t(4;14) were present in 5% and 11% of patients, respectively. The median number of prior therapies was 3. Eighty-seven percent (87%) of patients were refractory to lenalidomide, 80% refractory to proteasome inhibitor, 70% were refractory to both lenalidomide and proteasome inhibitor. Prior therapies included stem cell transplant (55%), bortezomib (100%), lenalidomide (99%), cyclophosphamide (66%), melphalan (63%), carfilzomib (21%), and daratumumab (3%).The efficacy of EMPLICITI was evaluated by progression-free survival (PFS) and overall response rate (ORR) as determined by the investigator. Efficacy results are shown in Table 13 and Figure 3. The median number of treatment cycles was for the EMPLICITI group and for the comparator arm with minimum follow-up of 9.1 months.Table 13:ELOQUENT-3 Efficacy ResultsEMPLICITI Pomalidomide/DexamethasoneN=60Pomalidomide/Dexamethasone N=57 p-value based on the log-rank test stratified by stage of disease at study entry (International Staging System I-II vs III) and number of prior lines of therapy (2-3 vs >=4) at randomization.+ International Myeloma Working Group (IMWG) criteria. p-value based on the Cochran-Mantel-Haenszel chi-square test stratified by stage of disease at study entry (International Staging System I-II vs III) and number of prior lines of therapy (2-3 vs >=4) at randomization. Complete response (CR) stringent complete response (sCR). EMPLICITIs interference with the assessment of myeloma protein with immunofixation and serum protein electrophoresis assay may interfere with correct response classification [see Drug Interactions (7)].NE=Non-EstimablePFSHazard Ratio [95% CI]0.54 [0.34, 0.86] Stratified log-rank test p-value 0.0078Median PFS in months [95% CI]10.25 [5.59, NE]4.67 [2.83, 7.16]ResponseOverall Response (ORR)+ (%) [95% CI]32 (53.3)[40.0, 66.3]15 (26.3)[15.5, 39.7] p-value 0.0029 Complete Response (CR sCR)+, (%)5 (8.3) (1.8) Very Good Partial Response (VGPR)+ (%)7 (11.7)4 (7.0) Partial Response (PR)+ (%)20 (33.3)10 (17.5)Figure 3: ELOQUENT-3 Progression-Free Survival empliciti-fig1. empliciti-fig2-s010. empliciti-fig3.

INFORMATION FOR PATIENTS SECTION.

17 PATIENT COUNSELING INFORMATION. Advise the patient to read the FDA-approved patient labeling (Patient Information).. Infusion Reactions. oEMPLICITI may cause infusion reactions. Advise patients to contact their healthcare provider if they experience signs and symptoms of infusion reactions, including fever, chills, rash, or breathing problems within 24 hours of infusion [see Warnings and Precautions (5.1) ].oAdvise patients that they will be required to take the following oral medications prior to EMPLICITI dosing to reduce the risk of infusion reaction [see Dosage and Administration (2.3)]:oDexamethasone orally as prescribedoH1 blocker: diphenhydramine or equivalent (if oral)oH2 blocker: ranitidine or equivalent (if oral)oAcetaminophen (650 to 1000 mg orally). oEMPLICITI may cause infusion reactions. Advise patients to contact their healthcare provider if they experience signs and symptoms of infusion reactions, including fever, chills, rash, or breathing problems within 24 hours of infusion [see Warnings and Precautions (5.1) ].. oAdvise patients that they will be required to take the following oral medications prior to EMPLICITI dosing to reduce the risk of infusion reaction [see Dosage and Administration (2.3)]:oDexamethasone orally as prescribedoH1 blocker: diphenhydramine or equivalent (if oral)oH2 blocker: ranitidine or equivalent (if oral)oAcetaminophen (650 to 1000 mg orally). oDexamethasone orally as prescribed. oH1 blocker: diphenhydramine or equivalent (if oral). oH2 blocker: ranitidine or equivalent (if oral). oAcetaminophen (650 to 1000 mg orally). Pregnancy. oAdvise patients that lenalidomide and pomalidomide have the potential to cause fetal harm and has specific requirements regarding contraception, pregnancy testing, blood and sperm donation, and transmission in sperm. Lenalidomide and pomalidomide are only available through REMS program [see Use in Specific Populations (8.1) ].. oAdvise patients that lenalidomide and pomalidomide have the potential to cause fetal harm and has specific requirements regarding contraception, pregnancy testing, blood and sperm donation, and transmission in sperm. Lenalidomide and pomalidomide are only available through REMS program [see Use in Specific Populations (8.1) ].. Infections. oInform patients of the risk of developing infections during treatment with EMPLICITI, and to report any symptoms of infection [see Warnings and Precautions (5.2) ].. oInform patients of the risk of developing infections during treatment with EMPLICITI, and to report any symptoms of infection [see Warnings and Precautions (5.2) ].. Second Primary Malignancies. oInform patients of the risk of developing SPM during treatment with EMPLICITI [see Warnings and Precautions (5.3)].. oInform patients of the risk of developing SPM during treatment with EMPLICITI [see Warnings and Precautions (5.3)].. Hepatotoxicity. oInform patients of the risk of hepatotoxicity during treatment with EMPLICITI and to report any signs and symptoms associated with this event to their healthcare provider for evaluation [see Warnings and Precautions (5.4) ]. Manufactured by:Bristol-Myers Squibb CompanyPrinceton, NJ 08543 USAU.S. License No. 1713. oInform patients of the risk of hepatotoxicity during treatment with EMPLICITI and to report any signs and symptoms associated with this event to their healthcare provider for evaluation [see Warnings and Precautions (5.4) ].. Manufactured by:Bristol-Myers Squibb CompanyPrinceton, NJ 08543 USAU.S. License No. 1713.

SPL PATIENT PACKAGE INSERT SECTION.

Patient InformationEMPLICITI(R) (em-plis-city)(elotuzumab)for injectionEMPLICITI is used with other prescription medicines called REVLIMID(R) (lenalidomide) and dexamethasone or POMALYST(R) (pomalidomide) and dexamethasone. Read the Medication Guide that comes with REVLIMID if used with REVLIMID and POMALYST if used with POMALYST. You can ask your healthcare provider or pharmacist for information about dexamethasone.What is EMPLICITIEMPLICITI is prescription medicine used to treat:omultiple myeloma in combination with the medicines REVLIMID (lenalidomide) and dexamethasone in adults who have received one to three prior treatments for their multiple myeloma.omultiple myeloma in combination with the medicines POMALYST (pomalidomide) and dexamethasone in adults who have received at least two prior treatments including REVLIMID (lenalidomide) and proteasome inhibitor.It is not known if EMPLICITI is safe and effective in children.Before you receive EMPLICITI, tell your healthcare provider about all of your medical conditions, including if you:ohave an infectionoare pregnant or plan to become pregnant. It is not known if EMPLICITI may harm your unborn baby. However, REVLIMID and POMALYST may cause birth defects or death of an unborn baby.oBefore receiving EMPLICITI with REVLIMID and dexamethasone, or EMPLICITI with POMALYST and dexamethasone, females and males must agree to the instructions in the REVLIMID REMS(R) program for the use of EMPLICITI in combination with REVLIMID and dexamethasone and the POMALYST REMS(R) program for the use of EMPLICITI in combination with POMALYST and dexamethasone. oThe REVLIMID REMS and POMALYST REMS programs have specific requirements about birth control (contraception), pregnancy testing, blood donation, and sperm donation that you need to know. Talk to your healthcare provider to learn more about REVLIMID or POMALYST.oare breastfeeding or plan to breastfeed. It is not known if EMPLICITI passes into breast milk. You should not breastfeed during treatment with EMPLICITI and REVLIMID and dexamethasone or EMPLICITI and POMALYST and dexamethasone.oTell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.How will receive EMPLICITIoEMPLICITI will be given to you by intravenous (IV) infusion into your vein.oYour EMPLICITI treatment schedule is divided into cycles that are 28 days (4 weeks) long. cycle includes the number of days you are on treatment and also the time you spend resting in between treatments.oEMPLICITI with REVLIMID and dexamethasone is usually given as follows:oCycles and (28 days per cycle), you will receive EMPLICITI one time every week.oCycles and up (28 days per cycle), you will receive EMPLICITI one time every weeks.oEMPLICITI with POMALYST and dexamethasone is usually given as follows:oCycle and (28 days per cycle), you will receive EMPLICITI one time every week.oCycle and up (28 days per cycle), you will receive EMPLICITI one time every weeks.oYour healthcare provider will decide how many treatments you will receive.oBefore every EMPLICITI infusion, you will receive medicines to help reduce the risk of infusion reactions.oIf you miss any appointments call your healthcare provider as soon as possible.What are the possible side effects of EMPLICITIEMPLICITI may cause serious side effects, including:oInfusion reactions. Infusion reactions can happen during your infusion or within 24 hours after your infusion of EMPLICITI. Your healthcare provider will give you medicines before each infusion of EMPLICITI to help reduce the risk of an infusion reaction. If you have an infusion reaction while receiving EMPLICITI, your healthcare provider will slow or stop your infusion and treat your reaction. If you have severe infusion reaction, your healthcare provider may stop your treatment completely. Tell your healthcare provider or get medical help right away if you have any of these symptoms after your infusion with EMPLICITI:ofeverochillsorashochest painotrouble breathingodizzinessolight-headednessoInfections. People with multiple myeloma who receive EMPLICITI with REVLIMID and dexamethasone or EMPLICITI with POMALYST and dexamethasone may develop infections that can be serious. Tell your healthcare provider right away if you have any signs and symptoms of an infection, including:ofeveroflu-like symptomsocoughoshortness of breathoburning with urinationoa painful skin rashoRisk of new cancers (malignancies). People with multiple myeloma who receive EMPLICITI with REVLIMID and dexamethasone or EMPLICITI with POMALYST and dexamethasone have risk of developing new cancers. Talk with your healthcare provider about your risk of developing new cancers if you receive EMPLICITI. Your healthcare provider will check you for new cancers during your treatment with EMPLICITI.oLiver problems. EMPLICITI may cause liver problems. Your healthcare provider will do blood tests to check your liver during treatment with EMPLICITI. Tell your healthcare provider if you have signs and symptoms of liver problems, including: tiredness, weakness, loss of appetite, yellowing of your skin or eyes, color changes in your stools, confusion, or swelling of the stomach area.The most common side effects of EMPLICITI when used with REVLIMID and dexamethasone include:ofatigueodiarrheaofeveroconstipationocoughonumbness, weakness, tingling, or burning pain in your arms or legsosore throat or runny noseoupper respiratory tract infectionodecreased appetiteopneumoniaThe most common side effects of EMPLICITI when used with POMALYST and dexamethasone include:oconstipationohigh blood sugarThese are not all of the possible side effects of EMPLICITI. 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 Bristol-Myers Squibb at 1-800-721-5072.General information about the safe and effective use of EMPLICITIMedicines are sometimes prescribed for purposes other than those listed in Patient Information leaflet.You can ask your pharmacist or healthcare provider for information about EMPLICITI that is written for health professionals.What are the ingredients of EMPLICITIActive ingredient: elotuzumabInactive ingredients: citric acid monohydrate, polysorbate 80, sodium citrate, sucroseFor more information, call 1-844-EMPLICITI (844-367-5424) or visit EMPLICITI.com. EMPLICITI(R) is trademark of Bristol-Myers Squibb Company. All other trademarks are the property of their respective owners.Manufactured by: Bristol-Myers Squibb Company, Princeton, NJ 08543 USAU.S. License No. 1713This Patient Information has been approved by the U.S. Food and Drug Administration.Revised: 11/2018. omultiple myeloma in combination with the medicines REVLIMID (lenalidomide) and dexamethasone in adults who have received one to three prior treatments for their multiple myeloma.. omultiple myeloma in combination with the medicines POMALYST (pomalidomide) and dexamethasone in adults who have received at least two prior treatments including REVLIMID (lenalidomide) and proteasome inhibitor.. ohave an infection. oare pregnant or plan to become pregnant. It is not known if EMPLICITI may harm your unborn baby. However, REVLIMID and POMALYST may cause birth defects or death of an unborn baby.oBefore receiving EMPLICITI with REVLIMID and dexamethasone, or EMPLICITI with POMALYST and dexamethasone, females and males must agree to the instructions in the REVLIMID REMS(R) program for the use of EMPLICITI in combination with REVLIMID and dexamethasone and the POMALYST REMS(R) program for the use of EMPLICITI in combination with POMALYST and dexamethasone. oThe REVLIMID REMS and POMALYST REMS programs have specific requirements about birth control (contraception), pregnancy testing, blood donation, and sperm donation that you need to know. Talk to your healthcare provider to learn more about REVLIMID or POMALYST.. oBefore receiving EMPLICITI with REVLIMID and dexamethasone, or EMPLICITI with POMALYST and dexamethasone, females and males must agree to the instructions in the REVLIMID REMS(R) program for the use of EMPLICITI in combination with REVLIMID and dexamethasone and the POMALYST REMS(R) program for the use of EMPLICITI in combination with POMALYST and dexamethasone. oThe REVLIMID REMS and POMALYST REMS programs have specific requirements about birth control (contraception), pregnancy testing, blood donation, and sperm donation that you need to know. Talk to your healthcare provider to learn more about REVLIMID or POMALYST.. oare breastfeeding or plan to breastfeed. It is not known if EMPLICITI passes into breast milk. You should not breastfeed during treatment with EMPLICITI and REVLIMID and dexamethasone or EMPLICITI and POMALYST and dexamethasone.. oTell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.. oEMPLICITI will be given to you by intravenous (IV) infusion into your vein.. oYour EMPLICITI treatment schedule is divided into cycles that are 28 days (4 weeks) long. cycle includes the number of days you are on treatment and also the time you spend resting in between treatments.. oEMPLICITI with REVLIMID and dexamethasone is usually given as follows:oCycles and (28 days per cycle), you will receive EMPLICITI one time every week.oCycles and up (28 days per cycle), you will receive EMPLICITI one time every weeks.. oCycles and (28 days per cycle), you will receive EMPLICITI one time every week.. oCycles and up (28 days per cycle), you will receive EMPLICITI one time every weeks.. oEMPLICITI with POMALYST and dexamethasone is usually given as follows:oCycle and (28 days per cycle), you will receive EMPLICITI one time every week.oCycle and up (28 days per cycle), you will receive EMPLICITI one time every weeks.. oCycle and (28 days per cycle), you will receive EMPLICITI one time every week.. oCycle and up (28 days per cycle), you will receive EMPLICITI one time every weeks.. oYour healthcare provider will decide how many treatments you will receive.. oBefore every EMPLICITI infusion, you will receive medicines to help reduce the risk of infusion reactions.. oIf you miss any appointments call your healthcare provider as soon as possible.. oInfusion reactions. Infusion reactions can happen during your infusion or within 24 hours after your infusion of EMPLICITI. Your healthcare provider will give you medicines before each infusion of EMPLICITI to help reduce the risk of an infusion reaction.. If you have an infusion reaction while receiving EMPLICITI, your healthcare provider will slow or stop your infusion and treat your reaction. If you have severe infusion reaction, your healthcare provider may stop your treatment completely. Tell your healthcare provider or get medical help right away if you have any of these symptoms after your infusion with EMPLICITI:. ofever. ochills. orash. ochest pain. otrouble breathing. odizziness. olight-headedness. oInfections. People with multiple myeloma who receive EMPLICITI with REVLIMID and dexamethasone or EMPLICITI with POMALYST and dexamethasone may develop infections that can be serious. Tell your healthcare provider right away if you have any signs and symptoms of an infection, including:. ofever. oflu-like symptoms. ocough. oshortness of breath. oburning with urination. oa painful skin rash. oRisk of new cancers (malignancies). People with multiple myeloma who receive EMPLICITI with REVLIMID and dexamethasone or EMPLICITI with POMALYST and dexamethasone have risk of developing new cancers. Talk with your healthcare provider about your risk of developing new cancers if you receive EMPLICITI. Your healthcare provider will check you for new cancers during your treatment with EMPLICITI.. oLiver problems. EMPLICITI may cause liver problems. Your healthcare provider will do blood tests to check your liver during treatment with EMPLICITI. Tell your healthcare provider if you have signs and symptoms of liver problems, including: tiredness, weakness, loss of appetite, yellowing of your skin or eyes, color changes in your stools, confusion, or swelling of the stomach area.. ofatigue. odiarrhea. ofever. oconstipation. ocough. onumbness, weakness, tingling, or burning pain in your arms or legs. osore throat or runny nose. oupper respiratory tract infection. odecreased appetite. opneumonia. oconstipation. ohigh blood sugar.

USE IN SPECIFIC POPULATIONS SECTION.

8 USE IN SPECIFIC POPULATIONS. Pregnancy: Embryo-fetal toxicity in combination with lenalidomide and dexamethasone or pomalidomide and dexamethasone. (8.1) 8.1 Pregnancy. Risk Summary. There are no available data on EMPLICITI use in pregnant women to inform drug associated risk of major birth defects and miscarriage. Animal reproduction studies have not been conducted with elotuzumab.EMPLICITI is administered in combination with lenalidomide and dexamethasone or pomalidomide and dexamethasone. Lenalidomide and pomalidomide can cause embryo-fetal harm and are contraindicated for use in pregnancy. Refer to the lenalidomide, pomalidomide and dexamethasone prescribing information for additional information. Lenalidomide and pomalidomide are only available through REMS program.The background risk of major birth defects and miscarriage for the indicated population is unknown. All pregnancies have background risk of birth defect, loss, or other adverse outcomes. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2-4% and 15-20%, respectively.. 8.2 Lactation. Risk Summary. There are no data on the presence of EMPLICITI in human milk, the effects on the breastfed child, or the effects on milk production. Because of the potential for serious adverse reactions in the breastfed child from elotuzumab administered in combination with lenalidomide and dexamethasone or pomalidomide and dexamethasone, advise lactating women not to breastfeed during treatment with EMPLICITI. Refer to the lenalidomide, pomalidomide and dexamethasone prescribing information for additional information.. 8.3 Females and Males of Reproductive Potential Pregnancy Testing. Refer to the lenalidomide and pomalidomide labeling for pregnancy testing requirements prior to initiating treatment in females of reproductive potential.When EMPLICITI is used with lenalidomide or pomalidomide, there is risk of fetal harm, including severe life-threatening human birth defects associated with lenalidomide and pomalidomide, and the need to follow requirements regarding pregnancy avoidance, including testing.. Contraception. FemalesRefer to the lenalidomide and pomalidomide labeling for contraception requirements prior to initiating treatment in females of reproductive potential.MalesLenalidomide and pomalidomide are present in the blood and semen of patients receiving the drug. Refer to the lenalidomide and pomalidomide full prescribing information for requirements regarding contraception and the prohibitions against blood and/or sperm donation due to presence and transmission in blood and/or semen and for additional information.. 8.4 Pediatric Use. Safety and effectiveness have not been established in pediatric patients.. 8.5 Geriatric Use. Of the 646 patients across treatment groups in the ELOQUENT-2 randomized trial designed to evaluate the use of EMPLICITI in combination with lenalidomide and low-dose dexamethasone in multiple myeloma, 57% were 65 years of age or older; the number of patients 65 years or older was similar between treatment groups. No overall differences in efficacy or safety were observed between patients 65 years or older and younger patients (less than 65 years of age).Of the 117 patients across treatment groups in the ELOQUENT-3 randomized trial designed to evaluate the use of EMPLICITI in combination with pomalidomide and low-dose dexamethasone in multiple myeloma, 62% were 65 years of age or older; the number of patients 65 years or older was similar between treatment groups. This study did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects.

WARNINGS AND PRECAUTIONS SECTION.

5 WARNINGS AND PRECAUTIONS. oInfusion reactions: Premedication is required. Interrupt EMPLICITI for Grade or higher and permanently discontinue for severe infusion reaction. (2.3, 2.4, 5.1)oInfections: Monitor for fever and other signs of infection and treat promptly. (5.2)oSecond Primary Malignancies (SPM): Higher incidences of SPM were observed in controlled clinical trial of patients with multiple myeloma receiving EMPLICITI. (5.3)oHepatotoxicity: Monitor liver function and stop EMPLICITI if hepatotoxicity is suspected. (5.4)oInterference with determination of complete response: EMPLICITI can interfere with assays used to monitor M-protein. This interference can impact the determination of complete response. (5.5). oInfusion reactions: Premedication is required. Interrupt EMPLICITI for Grade or higher and permanently discontinue for severe infusion reaction. (2.3, 2.4, 5.1). oInfections: Monitor for fever and other signs of infection and treat promptly. (5.2). oSecond Primary Malignancies (SPM): Higher incidences of SPM were observed in controlled clinical trial of patients with multiple myeloma receiving EMPLICITI. (5.3). oHepatotoxicity: Monitor liver function and stop EMPLICITI if hepatotoxicity is suspected. (5.4). oInterference with determination of complete response: EMPLICITI can interfere with assays used to monitor M-protein. This interference can impact the determination of complete response. (5.5). 5.1 Infusion Reactions. EMPLICITI can cause infusion reactions. Infusion reactions were reported in 10% of patients treated with EMPLICITI in the ELOQUENT-2 trial and 3.3% in the ELOQUENT-3 trial. In the ELOQUENT-2 trial, all reports of infusion reaction were Grade or lower. In the ELOQUENT-2 trial, Grade infusion reactions occurred in 1% of patients. The most common symptoms of an infusion reaction included fever, chills, and hypertension. Bradycardia and hypotension also developed during infusions.In the ELOQUENT-2 trial, 5% of patients required interruption of the administration of EMPLICITI for median of 25 minutes due to infusion reactions, and 1% of patients discontinued due to infusion reactions. Of the patients who experienced an infusion reaction, 70% (23/33) had them during the first dose.In the ELOQUENT-3 trial, the only infusion reaction symptom was chest discomfort (2%), which was Grade 1. All patients in the ELOQUENT-3 trial who experienced an infusion reaction had them during the first treatment cycle.Administer premedication consisting of dexamethasone, antihistamines (H1 and H2 blockers) and acetaminophen prior to EMPLICITI infusion [see Dosage and Administration (2.3)].Interrupt EMPLICITI infusion for Grade or higher infusion reactions and institute appropriate medical management [see Dosage and Administration (2.4)].. 5.2 Infections. In the ELOQUENT-2 trial (N=635), infections were reported in 81% of patients in EMPLICITI combined with lenalidomide and dexamethasone (E-Ld) arm and 74% in lenalidomide and dexamethasone (Ld). In the ELOQUENT-3 trial (N=115), infections were reported in 65% of patients in both EMPLICITI combined with pomalidomide and dexamethasone (E-Pd) arm and in pomalidomide and dexamethasone (Pd) arm. In the ELOQUENT-2 trial, Grade to infections were noted in 28% and 24% of E-Ld- and Ld-treated patients and in the ELOQUENT-3 trial, 13% and 22% of E-Pd- and Pd-treated patients, respectively. Discontinuations due to infections occurred in 3.5% of E-Ld-treated and 4.1% of Ld-treated patients in the ELOQUENT-2 trial and 7% of E-Pd-treated and 5% of Pd-treated patients in the ELOQUENT-3 trial. Fatal infections were reported in 2.5% and 2.2% of E-Ld- and Ld-treated patients in the ELOQUENT-2 trial and 5% and 3.6% of E-Pd- and Pd-treated patients in the ELOQUENT-3 trial.Opportunistic infections were reported in 22% of patients in the E-Ld arm and 13% of patients in the Ld arm in the ELOQUENT-2 trial and 10% of patients in the E-Pd arm and 9% of patients in the Pd arm in the ELOQUENT-3 trial. In the ELOQUENT-2 trial, fungal infections occurred in 10% of patients in the E-Ld arm and 5% of patients in the Ld arm. Herpes zoster was reported in 14% of patients treated with E-Ld and 7% of patients treated with Ld in the ELOQUENT-2 trial and 5% of patients treated with E-Pd and 1.8% of patients treated with Pd in the ELOQUENT-3 trial.Monitor patients for development of infections and treat promptly.. 5.3 Second Primary Malignancies In the ELOQUENT-2 trial (N=635), invasive second primary malignancies (SPM) have been observed in 9% of patients treated with E-Ld and 6% of patients treated with Ld and in the ELOQUENT-3 trial (N=115) in 1.8% of patients treated with Pd and in none of the patients treated with E-Pd. In the ELOQUENT-2 trial, the rate of hematologic malignancies were the same between E-Ld and Ld treatment arms (1.6%). Solid tumors were reported in 3.5% and 2.2% of E-Ld- and Ld-treated patients, respectively. Skin cancer was reported in 4.4% and 2.8% of patients treated with E-Ld and Ld, respectively. Monitor patients for the development of second primary malignancies.. 5.4 Hepatotoxicity In the ELOQUENT-2 trial (N=635), elevations in liver enzymes (aspartate transaminase/alanine transaminase [AST/ALT] greater than times the upper limit, total bilirubin greater than times the upper limit, and alkaline phosphatase less than times the upper limit) consistent with hepatotoxicity were reported in 2.5% and 0.6% of E-Ld- and Ld-treated patients. Two patients experiencing hepatotoxicity were not able to continue treatment; however, out of patients had resolution and were able to continue treatment. Monitor liver enzymes periodically. Stop EMPLICITI upon Grade or higher elevation of liver enzymes. After return to baseline values, continuation of treatment may be considered.. 5.5 Interference with Determination of Complete Response EMPLICITI is humanized IgG kappa monoclonal antibody that can be detected on both the serum protein electrophoresis (SPEP) and immunofixation (IFE) assays used for the clinical monitoring of endogenous M-protein [see Drug Interactions (7.2) ]. This interference can impact the determination of complete response and possibly relapse from complete response in patients with IgG kappa myeloma protein.