BESPONSA is indicated for the treatment of adults with relapsed or refractory B-cell precursor acute lymphoblastic leukemia (ALL).

4.2.1  Recommended Dosage

 

Pre-medicate before each dose [see 4.2 Posology and method of administration].

 

·        For the first cycle, the recommended total dose of BESPONSA for all patients is 1.8 mg/m² per cycle, administered as 3 divided doses on Day 1 (0.8 mg/m²), Day 8 (0.5 mg/m²), and Day 15 (0.5 mg/m²). Cycle 1 is 3 weeks in duration, but may be extended to 4 weeks if the patient achieves a complete remission (CR) or complete remission with incomplete hematologic recovery (CRi), and/or to allow recovery from toxicity.

 

·        For subsequent cycles:

 

·        In patients who achieve a CR or CRi, the recommended total dose of BESPONSA is 1.5 mg/m² per cycle, administered as 3 divided doses on Day 1 (0.5 mg/m²), Day 8 (0.5 mg/m²), and Day 15 (0.5 mg/m²). Subsequent cycles are 4 weeks in duration.

 

OR

 

·        In patients who do not achieve a CR or CRi, the recommended total dose of BESPONSA is 1.8 mg/m² per cycle given as 3 divided doses on Day 1 (0.8 mg/m²), Day 8 (0.5 mg/m²), and Day 15 (0.5 mg/m²). Subsequent cycles are 4 weeks in duration. Patients who do not achieve a CR or CRi within 3 cycles should discontinue treatment.

 

For patients proceeding to hematopoietic stem cell transplant (HSCT), the recommended duration of treatment with BESPONSA is 2 cycles. A third cycle may be considered for those patients who do not achieve CR or CRi and minimal residual disease (MRD) negativity after 2 cycles [see 4.4   Special warnings and precautions for use].

 

·        For patients not proceeding to HSCT, additional cycles of treatment, up to a maximum of 6 cycles, may be administered.

 

Table 1 shows the recommended dosing regimens.

 

Table 1.     Dosing Regimen for Cycle 1 and Subsequent Cycles Depending on Response to Treatment
	Day 1	Day 8a	Day 15a
Dosing regimen for Cycle 1
All patients:
Doseb	0.8 mg/m2	0.5 mg/m2	0.5 mg/m2
Cycle length	21 daysc
Dosing regimen for subsequent cycles depending on response to treatment
Patients who have achieved a CRd or CRie:
Doseb	0.5 mg/m2	0.5 mg/m2	0.5 mg/m2
Cycle length	28 daysf
Patients who have not achieved a CRd or CRie:
Doseb	0.8 mg/m2	0.5 mg/m2	0.5 mg/m2
Cycle length	28 daysf
Abbreviations: CR=complete remission; CRi=complete remission with incomplete hematologic recovery. a     +/- 2 days (maintain minimum of 6 days between doses). b     Dose is based on the patient’s body surface area (m2). c     For patients who achieve a CR or a CRi, and/or to allow for recovery from toxicity, the cycle length may be extended up to 28 days (i.e., 7-day treatment-free interval starting on Day 21). d     CR is defined as < 5% blasts in the bone marrow and the absence of peripheral blood leukemic blasts, full recovery of peripheral blood counts (platelets ≥ 100 × 109/L and absolute neutrophil counts [ANC] ≥ 1 × 109/L) and resolution of any extramedullary disease. e     CRi is defined as < 5% blasts in the bone marrow and the absence of peripheral blood leukemic blasts, incomplete recovery of peripheral blood counts (platelets < 100 × 109/L and/or ANC < 1 × 109/L) and resolution of any extramedullary disease. f      7-day treatment-free interval starting on Day 21.

 

 

4.2.2   Recommended Pre-medications and Cytoreduction

 

Premedication with a corticosteroid, antipyretic, and antihistamine is recommended prior to dosing. Patients should be observed during and for at least 1 hour after the end of infusion for symptoms of infusion related reactions [see 4.4           Special warnings and precautions for use].

·        For patients with circulating lymphoblasts, cytoreduction with a combination of hydroxyurea, steroids, and/or vincristine to a peripheral blast count of less than or equal to 10,000/mm³ is recommended prior to the first dose.

 

 

 

 

4.2.3 Dose Modification

 

Modify the dose of BESPONSA for toxicities (see Tables 2-4). BESPONSA doses within a treatment cycle (i.e., Days 8 and/or 15) do not need to be interrupted due to neutropenia or thrombocytopenia, but dosing interruptions within a cycle are recommended for non-hematologic toxicities. If the dose is reduced due to BESPONSA-related toxicity, the dose must not be re-escalated.

 

Table 2.     BESPONSA  Dose Modifications for Hematologic Toxicities
Criteria	BESPONSA Dose Modification(s)
If prior to BESPONSA treatment ANC was greater than or equal to 1 × 109/L	If ANC decreases, then interrupt the next cycle of treatment until recovery of ANC to greater than or equal to 1 × 109/L. Discontinue BESPONSA if low ANC persists for greater than 28 days and is suspected to be related to BESPONSA.
If prior to BESPONSA treatment platelet count was greater than or equal to 50 × 109/La	If platelet count decreases, then interrupt the next cycle of treatment until platelet count recovers to greater than or equal to 50 × 109/La. Discontinue BESPONSA if low platelet count persists for greater than 28 days and is suspected to be related to BESPONSA.
If prior to BESPONSA treatment ANC was less than 1 × 109/L and/or platelet count was less than 50 × 109/La	If ANC or platelet count decreases, then interrupt the next cycle of treatment until at least one of the following occurs: - ANC and platelet counts recover to at least baseline levels for the prior cycle, or - ANC recovers to greater than or equal to 1 × 109/L and platelet count recovers to greater than or equal to 50 × 109/La, or - Stable or improved disease (based on most recent bone marrow assessment) and the ANC and platelet count decrease is considered to be due to the underlying disease (not considered to be BESPONSA-related toxicity).
Abbreviation: ANC=absolute neutrophil count. a     Platelet count used for dosing should be independent of blood transfusion.

 

Table 3.      BESPONSA Dose Modifications for Non-hematologic Toxicities
Non-hematologic Toxicity	Dose Modification(s)
VOD or other severe liver toxicity	Permanently discontinue treatment [see 4.4        Special warnings and precautions for use].
Total bilirubin greater than 1.5 × ULN and AST/ALT greater than 2.5 × ULN	Interrupt dosing until recovery of total bilirubin to less than or equal to 1.5 × ULN and AST/ALT to less than or equal to 2.5 × ULN prior to each dose unless due to Gilbert’s syndrome or hemolysis. Permanently discontinue treatment if total bilirubin does not recover to less than or equal to 1.5 × ULN or AST/ALT does not recover to less than or equal to 2.5 × ULN [see 4.4Special warnings and precautions for use].
Infusion related reaction	Interrupt the infusion and institute appropriate medical management. Depending on the severity of the infusion related reaction, consider discontinuation of the infusion or administration of steroids and antihistamines. For severe or life-threatening infusion reactions, permanently discontinue treatment [see 4.4         Special warnings and precautions for use].
Non-hematologic toxicity greater than or equal to Grade 2a	Interrupt treatment until recovery to Grade 1 or pre-treatment grade levels prior to each dose.
Abbreviations: ALT=alanine aminotransferase; AST=aspartate aminotransferase; ULN=upper limit of normal; VOD=venoocclusive disease. a     Severity grade according to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) version 3.0.

 

Table 4.     BESPONSA Dose Modifications Depending on Duration of Dosing Interruption Due to Non-Hematologic Toxicity Toxicities
Duration of Dose Interruption Due to Toxicity	Dose Modification(s)
Less than 7 days (within a cycle)	Interrupt the next dose (maintain a minimum of 6 days between doses).
Greater than or equal to 7 days	Omit the next dose within the cycle.
Greater than or equal to 14 days	Once adequate recovery is achieved, decrease the total dose by 25% for the subsequent cycle. If further dose modification is required, then reduce the number of doses to 2 per cycle for subsequent cycles. If a 25% decrease in the total dose followed by a decrease to 2 doses per cycle is not tolerated, then permanently discontinue treatment.
Greater than 28 days	Consider permanent discontinuation of treatment.

None.

4.4.1    Hepatotoxicity, Including Hepatic Veno-occlusive Disease (VOD) (also known as Sinusoidal Obstruction Syndrome)

 

In the INO‑VATE ALL trial, hepatotoxicity, including severe, life‑threatening, and sometimes fatal hepatic VOD was observed in 23/164 patients (14%) in the BESPONSA arm during or following treatment or following a HSCT after completion of treatment. VOD was reported up to 56 days after the last dose during treatment or during follow‑up without an intervening HSCT. The median time from subsequent HSCT to onset of VOD was 15 days (range: 3‑57 days). In the BESPONSA arm, among the 79 patients who proceeded to a subsequent HSCT, VOD was reported in 18/79 patients (23%), and among all 164 patients treated, VOD was reported in 5/164 patients (3%) during study therapy or in follow-up without an intervening HSCT.

 

The risk of VOD was greater in patients who underwent HSCT after BESPONSA treatment; use of HSCT conditioning regimens containing 2 alkylating agents (e.g., busulfan in combination with other alkylating agents) and last total bilirubin level greater than or equal to the ULN before HSCT are significantly associated with an increased risk of VOD. Other risk factors for VOD in patients treated with BESPONSA included ongoing or prior liver disease, prior HSCT, increased age, later salvage lines, and a greater number of BESPONSA treatment cycles. Patients who have experienced prior VOD or have serious ongoing hepatic liver disease (e.g., cirrhosis, nodular regenerative hyperplasia, active hepatitis) are at an increased risk for worsening of liver disease, including developing VOD, following treatment with BESPONSA.

 

Monitor closely for signs and symptoms of VOD; these may include elevations in total bilirubin, hepatomegaly (which may be painful), rapid weight gain, and ascites. Due to the risk of VOD, for patients proceeding to HSCT, the recommended duration of treatment with BESPONSA is 2 cycles; a third cycle may be considered for those patients who do not achieve a CR or CRi and MRD negativity after 2 cycles [see 4.2 Posology and method of administration]. For patients who proceed to HSCT, monitor liver tests closely during the first month post‑HSCT, then less frequently thereafter, according to standard medical practice.

 

In the INO‑VATE ALL trial, increases in liver tests were reported. Grade 3/4 AST, ALT, and total bilirubin abnormal liver tests occurred in 7/160 (4%), 7/161 (4%), and 8/161 patients (5%), respectively. 

 

In all patients, monitor liver tests, including ALT, AST, total bilirubin, and alkaline phosphatase, prior to and following each dose of BESPONSA. Elevations of liver tests may require dosing interruption, dose reduction, or permanent discontinuation of BESPONSA  [see 4.2 Posology and method of administration].

 

4.4.2    Increased Risk of Post-Transplant Non-Relapse Mortality

 

In the INO‑VATE ALL trial, a higher post-HSCT non-relapse mortality rate was observed in patients receiving BESPONSA compared to the Investigator’s choice of chemotherapy arm, resulting in a higher Day 100 post-HSCT mortality rate.

 

Overall, 79/164 patients (48%) in the BESPONSA arm and 35/162 patients (22%) in the Investigator’s choice of chemotherapy arm had a follow-up HSCT. The post-HSCT non-relapse mortality rate was 31/79 (39%) and 8/35 (23%) in the BESPONSA arm compared to the Investigator’s choice of chemotherapy arm, respectively.

 

In the BESPONSA arm, the most common causes of post-HSCT non-relapse mortality included VOD and infections. Five of the 18 VOD events that occurred post-HSCT were fatal. In the BESPONSA arm, among patients with ongoing VOD at time of death, 6 patients died due to multiorgan failure (MOF) or infection (3 patients died due to MOF, 2 patients died due to infection, and 1 patient died due to MOF and infection).

 

Monitor closely for toxicities post-HSCT, including signs and symptoms of infection and VOD [see 4.4 Special warnings and precautions for use].

 

4.4.3    Myelosuppression

 

In the INO‑VATE ALL trial, myelosuppression was observed in patients receiving BESPONSA [see Adverse Reactions (6.1)].

 

Thrombocytopenia and neutropenia were reported in 83/164 patients (51%) and 81/164 patients (49%), respectively. Grade 3 thrombocytopenia and neutropenia were reported in 23/164 patients (14%) and 33/164 patients (20%), respectively. Grade 4 thrombocytopenia and neutropenia were reported in 46/164 patients (28%) and 45/164 patients (27%), respectively. Febrile neutropenia, which may be life‑threatening, was reported in 43/164 patients (26%). For patients who were in CR or CRi at the end of treatment, the recovery of platelet counts to > 50,000/mm³ was later than 45 days after the last dose in 15/164 patients (9%) who received BESPONSA and 3/162 patients (2%) who received Investigator’s choice of chemotherapy.

 

4.8         Complications associated with myelosuppression (including infections and bleeding/hemorrhagic events) were observed in patients receiving BESPONSA [see 4.8 Undesirable effects]. Infections, including serious infections, some of which were life-threatening or fatal, were reported in 79/164 patients (48%). Fatal infections, including pneumonia, neutropenic sepsis, sepsis, septic shock, and pseudomonal sepsis, were reported in 8/164 patients (5%). Bacterial, viral, and fungal infections were reported.

 

Hemorrhagic events were reported in 54/164 patients (33%). Grade 3 or 4 hemorrhagic events were reported in 8/164 patients (5%). One Grade 5 (fatal) hemorrhagic event (intra-abdominal hemorrhage) was reported in 1/164 patients (1%). The most common hemorrhagic event was epistaxis which was reported in 24/164 patients (15%).

 

Monitor complete blood counts prior to each dose of BESPONSA and monitor for signs and symptoms of infection, bleeding/hemorrhage, or other effects of myelosuppression during treatment with BESPONSA. As appropriate, administer prophylactic anti‑infectives and employ surveillance testing during and after treatment with BESPONSA. Management of severe infection, bleeding/hemorrhage, or other effects of myelosuppression, including severe neutropenia or thrombocytopenia, may require dosing interruption, dose reduction, or permanent discontinuation of BESPONSA [see Dosage and Administration (2.3)].

 

4.4.4    Infusion Related Reactions

 

In the INO‑VATE ALL trial, infusion related reactions were observed in patients who received BESPONSA. Infusion related reactions (all Grade 2) were reported in 4/164 patients (2%). Infusion related reactions generally occurred in Cycle 1 shortly after the end of the BESPONSA infusion and resolved spontaneously or with medical management.

 

Premedicate with a corticosteroid, antipyretic, and antihistamine prior to dosing [see 4.2   Posology and method of administration].

 

Monitor patients closely during and for at least 1 hour after the end of infusion for the potential onset of infusion related reactions, including symptoms such as fever, chills, rash, or breathing problems. Interrupt infusion and institute appropriate medical management if an infusion related reaction occurs. Depending on the severity of the infusion related reaction, consider discontinuation of the infusion or administration of steroids and antihistamines. For severe or life‑threatening infusion reactions, permanently discontinue BESPONSA [see 4.2 Posology and method of administration].

 

4.4.5    QT Interval Prolongation

 

In the INO‑VATE ALL trial, increases in QT interval corrected for heart rate using Fridericia’s formula (QTcF) of ≥ to 60 msec from baseline were measured in 4/162 patients (3%). No patients had QTcF values greater than 500 msec [see  5.   PHARMACOLOGICAL PROPERTIES]. Grade 2 QT prolongation was reported in 2/164 patients (1%). No ≥ Grade 3 QT prolongation or events of Torsade de Pointes were reported [see 4.8 Undesirable effects].

 

Administer BESPONSA with caution in patients who have a history of or predisposition for QTc prolongation, who are taking medicinal products that are known to prolong QT interval [see Drug Interactions (7)], and in patients with electrolyte disturbances [see Drug Interactions (7)]. Obtain electrocardiograms (ECGs) and electrolytes prior to the start of treatment, after initiation of any drug known to prolong QTc, and periodically monitor as clinically indicated during treatment [see 4.5 Interaction with other medicinal products and other forms of interaction , 5.1 Pharmacodynamics properties ].

 

4.4.6    Embryo‑Fetal Toxicity

 

Based on its mechanism of action and findings from animal studies, BESPONSA can cause embryo‑fetal harm when administered to a pregnant woman. In animal studies, inotuzumab ozogamicin caused embryo‑fetal toxicities, starting at a dose that was approximately 0.4 times the exposure in patients at the maximum recommended dose, based on the area under the concentration‑time curve (AUC). Advise females of reproductive potential to use effective contraception during treatment with BESPONSA and for at least 8 months after the final dose of BESPONSA. Advise males with female partners of reproductive potential to use effective contraception during treatment with BESPONSA and for at least 5 months after the last dose of BESPONSA. Apprise pregnant women of the potential risk to the fetus. Advise women to contact their healthcare provider if they become pregnant or if pregnancy is suspected during treatment with BESPONSA [see 4.6 Fertility, Pregnancy and Lactation , 5. Pharmacological Properties , 5.3 Preclinical safety data  ].

 

 

Drugs That Prolong the QT Interval

 

Concomitant use of BESPONSA with drugs known to prolong the QT interval or induce Torsades de Pointes may increase the risk of a clinically significant QTc interval prolongation [see 5.1 Pharmacodynamics properties]. Discontinue or use alternative concomitant drugs that do not prolong QT/QTc interval while the patient is using BESPONSA. When it is not feasible to avoid concomitant use of drugs known to prolong QT/QTc, obtain ECGs and electrolytes prior to the start of treatment, after initiation of any drug known to prolong QTc, and periodically monitor as clinically indicated during treatment [see 4.4 Special warnings and precautions for use ].

 

4.6.1    Pregnancy

 

Risk Summary

 

Based on its mechanism of action and findings from animal studies [see 5. Pharmacological properties], Nonclinical Toxicology (13.1)], BESPONSA can cause embryo‑fetal harm when administered to a pregnant woman. There are no available data on BESPONSA use in pregnant women to inform a drug‑associated risk of major birth defects and miscarriage. In rat embryo‑fetal development studies, inotuzumab ozogamicin caused embryo‑fetal toxicity at maternal systemic exposures that were ≥ 0.4 times the exposure in patients at the maximum recommended dose, based on AUC [see Data]. If this drug is used during pregnancy, or if the patient becomes pregnant while taking this drug, advise the patient of the potential risk to a fetus.

 

Adverse outcomes in pregnancy occur regardless of the health of the mother or the use of medications. The estimated background risk of major birth defects and miscarriage for the indicated population is unknown. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies are 2-4% and 15-20%, respectively.

 

Data

 

Animal Data

 

In embryo‑fetal development studies in rats, pregnant animals received daily intravenous doses of inotuzumab ozogamicin up to 0.36 mg/m² during the period of organogenesis. Embryo-fetal toxicities including increased resorptions and fetal growth retardation as evidenced by decreased live fetal weights and delayed skeletal ossification were observed at ≥ 0.11 mg/m² (approximately 2 times the exposure in patients at the maximum recommended dose, based on AUC). Fetal growth retardation also occurred at 0.04 mg/m² (approximately 0.4 times the exposure in patients at the maximum recommended dose, based on AUC).

 

In an embryo-fetal development study in rabbits, pregnant animals received daily intravenous doses up to 0.15 mg/m² (approximately 3 times the exposure in patients at the maximum recommended dose, based on AUC) during the period of organogenesis. At a dose of 0.15 mg/m², slight maternal toxicity was observed in the absence of any effects on embryo‑fetal development.

 

4.6.2    Lactation

 

Risk Summary

 

There are no data on the presence of inotuzumab ozogamicin or its metabolites in human milk, the effects on the breastfed infant, or the effects on milk production.  Because of the potential for adverse reactions in breastfed infants, advise women not to breastfeed during treatment with BESPONSA and for at least 2 months after the last dose.

 

4.6.3    Females and Males of Reproductive Potential

 

Pregnancy Testing

 

Based on its mechanism of action and findings from animal studies, BESPONSA can cause embryo‑fetal harm when administered to a pregnant woman [see 4.6 Fertility, Pregnancy and Lactation , 5.3 Preclinical safety data ] Verify the pregnancy status of females of reproductive potential prior to initiating BESPONSA.

 

Contraception

 

Females

 

Advise females of reproductive potential to avoid becoming pregnant while receiving BESPONSA. Advise females of reproductive potential to use effective contraception during treatment with BESPONSA and for at least 8 months after the last dose [see 5.3 Preclinical safety data ].

 

Males

 

Advise males with female partners of reproductive potential to use effective contraception during treatment with BESPONSA and for at least 5 months after the last dose [see 5.3 Preclinical safety data].

 

Infertility

 

Females

 

Based on findings in animals, BESPONSA may impair fertility in females of reproductive potential [see 5.3 Preclinical safety data ].

 

Males

 

Based on findings in animals, BESPONSA may impair fertility in males of reproductive potential [see 5.3 Preclinical safety data ].

 

4.6.4    Pediatric Use

 

Safety and effectiveness have not been established in pediatric patients.

 

4.6.5    Geriatric Use

 

In the INO-VATE ALL trial, 30/164 patients (18%) treated with BESPONSA were ≥ 65 years of age. No differences in responses were identified between older and younger patients.

 

Based on a population pharmacokinetic analysis in 765 patients, no adjustment to the starting dose is required based on age [see  5.3 Preclinical safety data ].

 

4.6.6    Hepatic Impairment

 

Based on a population pharmacokinetic analysis, the clearance of inotuzumab ozogamicin in patients with mild hepatic impairment (total bilirubin less than or equal to ULN and AST greater than ULN, or total bilirubin greater than 1.0‑1.5 × ULN and AST any level; n=150) was similar to patients with normal hepatic function (total bilirubin/AST less than or equal to ULN; n=611). In patients with moderate (total bilirubin greater than 1.5‑3 × ULN and AST any level; n=3) and severe hepatic impairment (total bilirubin greater than 3 × ULN and AST any level; n=1), inotuzumab ozogamicin clearance did not appear to be reduced [see 5.3 Preclinical safety data ].

 

No adjustment to the starting dose is required when administering BESPONSA to patients with total bilirubin less than or equal to 1.5 × ULN and AST/ALT less than or equal to 2.5 × ULN [see 4.2 Posology and method of adminstration]. There is limited safety information available in patients with total bilirubin greater than 1.5 × ULN and/or AST/ALT greater than 2.5 × ULN prior to dosing. Interrupt dosing until recovery of total bilirubin to less than or equal to 1.5 × ULN and AST/ALT to less than or equal to 2.5 × ULN prior to each dose unless due to Gilbert’s syndrome or hemolysis. Permanently discontinue treatment if total bilirubin does not recover to less than or equal to 1.5 × ULN or AST/ALT does not recover to less than or equal to 2.5 × ULN [see 4.2 Posology and method of administration , 4.4 Special warnings and precautions for use ].

 

 

 

 

Not applicable

ADVERSE REACTIONS

 

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

 

·        Hepatotoxicity, including hepatic VOD (also known as SOS) [see 4.4 Special warnings and precautions for use ]

·        Increased risk of post-transplant non-relapse mortality [see 4.4 Special warnings and precautions for use ]

·        Myelosuppression [see 4.4 Special warnings and precautions for use ]

·        Infusion related reactions [see 4.4 Special warnings and precautions for use ]

·        QT interval prolongation [see 4.4 Special warnings and precautions for use ]

 

4.8.1    Clinical Trials Experience

 

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

 

The adverse reactions described in this section reflect exposure to BESPONSA in 164 patients with relapsed or refractory ALL who participated in a randomized clinical study of BESPONSA versus Investigator’s choice of chemotherapy (fludarabine + cytarabine + granulocyte colony-stimulating factor [FLAG], mitoxantrone + cytarabine [MXN/Ara-C], or high dose cytarabine [HIDAC]) (INO‑VATE ALL Trial [NCT01564784]) [see 5.4 Clinical studies ].

 

Of the 164 patients who received BESPONSA, the median age was 47 years (range: 18‑78 years), 56% were male, 68% had received 1 prior treatment regimen for ALL, 31% had received 2 prior treatment regimens for ALL, 68% were White, 19% were Asian, and 2% were Black.

 

In patients who received BESPONSA, the median duration of treatment was 8.9 weeks (range: 0.1‑26.4 weeks), with a median of 3 treatment cycles started in each patient. In patients who received Investigator’s choice of chemotherapy, the median duration of treatment was 0.9 weeks (range: 0.1‑15.6 weeks), with a median of 1 treatment cycle started in each patient.

In patients who received BESPONSA, the most common (≥ 20%) adverse reactions were thrombocytopenia, neutropenia, infection, anemia, leukopenia, fatigue, hemorrhage, pyrexia, nausea, headache, febrile neutropenia, transaminases increased, abdominal pain, gamma-glutamyltransferase increased, and hyperbilirubinemia.

 

In patients who received BESPONSA, the most common (≥ 2%) serious adverse reactions were infection, febrile neutropenia, hemorrhage, abdominal pain, pyrexia, VOD, and fatigue.

 

In patients who received BESPONSA, the most common (≥ 2%) adverse reactions reported as the reason for permanent discontinuation were infection (6%), thrombocytopenia (2%), hyperbilirubinemia (2%), transaminases increased (2%), and hemorrhage (2%); the most common (≥ 5%) adverse reactions reported as the reason for dosing interruption were neutropenia (17%), infection (10%), thrombocytopenia (10%), transaminases increased (6%), and febrile neutropenia (5%); and the most common (≥ 1%) adverse reactions reported as the reason for dose reduction were neutropenia (1%), thrombocytopenia (1%), and transaminases increased (1%).

 

VOD was reported in 23/164 patients (14%) who received BESPONSA during or following treatment or following a HSCT after completion of treatment [see 4.4 Special warnings and Precautions for use ].

 

Table 6 shows the adverse reactions with ≥ 10% incidence reported in patients with relapsed or refractory ALL who received BESPONSA or Investigator’s choice of chemotherapy.

 

Table 6.     Adverse Reactions With ≥ 10% Incidencea in Patients With Relapsed or Refractory B‑Cell Precursor ALL Who Received BESPONSA or Investigator’s Choice of Chemotherapy (FLAG, MXN/Ara-C, or HIDAC)
Body System Adverse Reaction	BESPONSA (N=164)		FLAG, MXN/Ara-C, or HIDAC (N=143b)
	All Grades	≥ Grade 3	All Grades	≥ Grade 3
	%	%	%	%
Infections
Infectionc	48	28	76	54
Blood and lymphatic system disorders
Thrombocytopeniad	51	42	61	59
Neutropeniae	49	48	45	43
Anemiaf	36	24	59	47
Leukopeniag	35	33	43	42
Febrile neutropenia	26	26	53	53
Lymphopeniah	18	16	27	26
Metabolism and nutrition disorders
Decreased appetite	12	1	13	2
Nervous system disorders
Headachei	28	2	27	1
Vascular disorders
Hemorrhagej	33	5	28	5
Gastrointestinal disorders
Nausea	31	2	46	0
Abdominal paink	23	3	23	1
Diarrhea	17	1	38	1
Constipation	16	0	24	0
Vomiting	15	1	24	0
Stomatitisl	13	2	26	3
Hepatobiliary disorders
Hyperbilirubinemia	21	5	17	6
General disorders and administration site conditions
Fatiguem	35	5	25	3
Pyrexia	32	3	42	6
Chills	11	0	11	0
Investigations
Transaminases increasedn	26	7	13	5
Gamma-glutamyltransferase increased	21	10	8	4
Alkaline phosphatase increased	13	2	7	0
Adverse reactions included treatment-emergent all-causality events that commenced on or after Cycle 1 Day 1 within 42 days after the last dose of BESPONSA, but prior to the start of a new anticancer treatment (including HSCT). Preferred terms were retrieved by applying the Medical Dictionary for Regulatory Activities (MedDRA) version 18.1. Severity grade of adverse reactions were according to NCI CTCAE version 3.0. Abbreviations: ALL=acute lymphoblastic leukemia; FLAG=fludarabine + cytarabine + granulocyte colony-stimulating factor; HIDAC=high dose cytarabine; HSCT=hematopoietic stem cell transplant; MXN/Ara-C=mitoxantrone + cytarabine; N=number of patients; NCI CTCAE=National Cancer Institute Common Toxicity Criteria for Adverse Events. a   Only adverse reactions with ≥ 10% incidence in the BESPONSA arm are included. b   19 patients randomized to FLAG, MXN/Ara-C, or HIDAC did not receive treatment. c   Infection includes any reported preferred terms for BESPONSA retrieved in the System Organ Class Infections and infestations. d   Thrombocytopenia includes the following reported preferred terms: Platelet count decreased and Thrombocytopenia. e   Neutropenia includes the following reported preferred terms: Neutropenia and Neutrophil count decreased. f    Anemia includes the following reported preferred terms: Anemia and Hemoglobin decreased. g   Leukopenia includes the following reported preferred terms: Leukopenia, Monocytopenia, and White blood cell count decreased. h   Lymphopenia includes the following reported preferred terms: B-lymphocyte count decreased, Lymphocyte count decreased, and Lymphopenia. i    Headache includes the following reported preferred terms: Headache, Migraine, and Sinus headache. j    Hemorrhage includes reported preferred terms for BESPONSA retrieved in the Standard MedDRA Query (narrow) for Hemorrhage terms (excluding laboratory terms), resulting in the following preferred terms: Conjunctival hemorrhage, Contusion, Ecchymosis, Epistaxis, Eyelid bleeding, Gastrointestinal hemorrhage, Gastritis hemorrhagic, Gingival bleeding, Hematemesis, Hematochezia, Hematotympanum, Hematuria, Hemorrhage intracranial, Hemorrhage subcutaneous, Hemorrhoidal hemorrhage, Intra-abdominal hemorrhage, Lip hemorrhage, Lower gastrointestinal hemorrhage, Mesenteric hemorrhage, Metrorrhagia, Mouth hemorrhage, Muscle hemorrhage, Oral mucosa hematoma, Petechiae, Post‑procedural hematoma, Rectal hemorrhage, Shock hemorrhagic, Subcutaneous hematoma, Subdural hematoma, Upper gastrointestinal hemorrhage, and Vaginal hemorrhage. k   Abdominal pain includes the following reported preferred terms: Abdominal pain, Abdominal pain lower, Abdominal pain upper, Abdominal tenderness, Esophageal pain, and Hepatic pain. l    Stomatitis includes the following reported preferred terms: Aphthous ulcer, Mucosal inflammation, Mouth ulceration, Oral pain, Oropharyngeal pain, and Stomatitis. m  Fatigue includes the following reported preferred terms: Asthenia and Fatigue. n   Transaminases increased includes the following reported preferred terms: Aspartate aminotransferase increased, Alanine aminotransferase increased, Hepatocellular injury, and Hypertransaminasemia.

 

Additional adverse reactions (all grades) that were reported in less than 10% of patients treated with BESPONSA included: lipase increased (9%), abdominal distension (6%), amylase increased (5%), hyperuricemia (4%), ascites (4%), infusion related reaction (2%; includes the following: hypersensitivity and infusion related reaction), pancytopenia (2%; includes the following: bone marrow failure, febrile bone marrow aplasia, and pancytopenia), tumor lysis syndrome (2%), and electrocardiogram QT prolonged (1%).

 

Table 7 shows the clinically important laboratory abnormalities reported in patients with relapsed or refractory ALL who received BESPONSA or Investigator’s choice of chemotherapy.

 

Table 7.     Laboratory Abnormalities in Patients With Relapsed or Refractory B-Cell Precursor ALL Who Received BESPONSA or Investigator’s Choice of Chemotherapy (FLAG, MXN/Ara-C, or HIDAC)
Laboratory Abnormalitya	N	BESPONSA		N	FLAG, MXN/Ara-C, or HIDAC
		All Grades	Grade 3/4		All Grades	Grade 3/4
		%	%		%	%
Hematology
Platelet count decreased	161	98	76	142	100	99
Hemoglobin decreased	161	94	40	142	100	70
Leukocytes decreased	161	95	82	142	99	98
Neutrophil count decreased	160	94	86	130	93	88
Lymphocytes (absolute) decreased	160	93	71	127	97	91
Chemistry
GGT increased	148	67	18	111	68	17
AST increased	160	71	4	134	38	4
ALP increased	158	57	1	133	52	3
ALT increased	161	49	4	137	46	4
Blood bilirubin increased	161	36	5	138	35	6
Lipase increased	139	32	13	90	20	2
Hyperuricemia	158	16	3	122	11	0
Amylase increased	143	15	2	102	9	1
Severity grade of laboratory abnormalities according to NCI CTCAE version 3.0.
Abbreviations: ALL=acute lymphoblastic leukemia; ALP=alkaline phosphatase; ALT=alanine aminotransferase; AST=aspartate aminotransferase; FLAG=fludarabine + cytarabine + granulocyte colony-stimulating factor; GGT=gamma-glutamyltransferase; HIDAC=high dose cytarabine; MXN/Ara-C=mitoxantrone + cytarabine; N=number of patients; NCI CTCAE=National Cancer Institute Common Toxicity Criteria for Adverse Events.
a Laboratory abnormalities were summarized up to the end of treatment + 42 days but prior to the start of a new anti-cancer therapy.

 

4.8.2    Immunogenicity

 

As with all therapeutic proteins, there is potential for immunogenicity. The detection of antibody formation is highly dependent on the sensitivity and specificity of the assay. Additionally, the observed incidence of antibody (including neutralizing antibody) positivity in an assay may be influenced by several factors including assay methodology, sample handling, timing of sample collection, concomitant medications, and underlying disease. For these reasons, comparison of the incidence of antibodies to inotuzumab ozogamicin in the studies described below with the incidence of antibodies in other studies or to other products may be misleading.

 

In clinical studies of BESPONSA in patients with relapsed or refractory ALL, the immunogenicity of BESPONSA was evaluated using an electrochemiluminescence (ECL)‑based immunoassay to test for anti-inotuzumab ozogamicin antibodies. For patients whose sera tested positive for anti‑inotuzumab ozogamicin antibodies, a cell‑based luminescence assay was performed to detect neutralizing antibodies.

 

In clinical studies of BESPONSA in patients with relapsed or refractory ALL, 7/236 patients (3%) tested positive for anti‑inotuzumab ozogamicin antibodies. No patients tested positive for neutralizing anti‑inotuzumab ozogamicin antibodies. In patients who tested positive for anti‑inotuzumab ozogamicin antibodies, the presence of anti‑inotuzumab ozogamicin antibodies did not affect clearance following BESPONSA treatment.

 

 

 

Reporting of adverse reactions

Reporting suspected adverse reactions after marketing authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions according to their local requirements.

 

 

To Report side effects

 

• Saudi Arabia

 

National Pharmacovigilance and Drug Safety Centre ( NPC ) Fax: +966 11 205 7662 Call NPC at 00966 11 2038222, Exts: 2317-2356-2353-2354-2334-2340 Toll-Free phone: 8002490000 E-mail: npc.drug@sfda.gov.sa Website: www.sfda.gov.sa/npc

 

Not applicable

Pharmacodynamics

 

During the treatment period, the pharmacodynamic response to BESPONSA was characterized by the depletion of CD22-positive leukemic blasts.

 

Cardiac Electrophysiology

 

In a randomized clinical study in patients with relapsed or refractory ALL, increases in QTcF of ≥ 60 msec from baseline were measured in 4/162 patients (3%) in the BESPONSA arm and 3/124 patients (2%)  in the Investigator’s choice of chemotherapy arm. Increases in QTcF of > 500 msec were observed in none of the patients in the BESPONSA arm and 1/124 patients (1%) in the Investigator’s choice of chemotherapy arm. Central tendency analysis of the QTcF interval changes from baseline showed that the highest mean (upper bound of the 2‑sided 90% CI) for QTcF was 15.3 (21.1) msec, which was observed at Cycle 4/Day 1/1 hour in the BESPONSA arm [see 4.4 Special warnings and precautions for use ].

The mean C_max of inotuzumab ozogamicin was 308 ng/mL. The mean simulated total AUC per cycle was 100,000 ngŸh/mL. In patients with relapsed or refractory ALL, steady-state drug concentration was achieved by Cycle 4. Following administration of multiple doses, a 5.3 times accumulation of inotuzumab ozogamicin was predicted by Cycle 4.

 

Distribution

 

N-acetyl-gamma-calicheamicin dimethylhydrazide is approximately 97% bound to human plasma proteins in vitro. In humans, the total volume of distribution of inotuzumab ozogamicin was approximately 12 L.

 

Elimination

 

The pharmacokinetics of inotuzumab ozogamicin was well characterized by a 2‑compartment model with linear and time-dependent clearance components. In 234 patients with relapsed or refractory ALL, the clearance of inotuzumab ozogamicin at steady state was 0.0333 L/h and the terminal half‑life (t_½) was 12.3 days. Following administration of multiple doses, a 5.3 times accumulation of inotuzumab ozogamicin was predicted by Cycle 4.

 

Metabolism

 

In vitro, N-acetyl-gamma-calicheamicin dimethylhydrazide was primarily metabolized via nonenzymatic reduction. In humans, N-acetyl-gamma-calicheamicin dimethylhydrazide serum levels were typically below the limit of quantitation.

 

Specific Populations
 

The effect of intrinsic factors on inotuzumab ozogamicin pharmacokinetics was assessed using a population pharmacokinetic analysis unless otherwise specified. Age (18 to 92 years of age), sex, and race (Asian versus non-Asian [Caucasian, Black, and Unspecified]) had no clinically significant effect on the pharmacokinetics of inotuzumab ozogamicin. Body surface area was found to significantly affect inotuzumab ozogamicin disposition. BESPONSA is dosed based on body surface area [see 4.2 Posology and method of administration].

 

Patients with Renal Impairment

 

The clearance of inotuzumab ozogamicin in patients with mild renal impairment (creatinine clearance [CL_cr; based on the Cockcroft-Gault formula] 60‑89 mL/min; n=237), moderate renal impairment (CL_cr 30‑59 mL/min; n=122), or severe renal impairment (CL_cr 15‑29 mL/min; n=4) was similar to patients with normal renal function (CL_cr ≥90 mL/min; n=402). The safety and efficacy of inotuzumab ozogamicin in patients with end stage renal disease with or without hemodialysis is unknown.

 

Patients with Hepatic Impairment

 

The clearance of inotuzumab ozogamicin in patients with mild hepatic impairment (total bilirubin ≤ULN and AST > ULN, or total bilirubin >1.0‑1.5 × ULN and AST any level; n=150) was similar to patients with normal hepatic function (total bilirubin/AST ≤ULN; n=611). There is insufficient data in patients with moderate and severe hepatic impairment (total bilirubin >1.5 ULN).

 

Drug Interactions

 

In vitro

 

Effect of Metabolic Pathways and Transporter Systems on BESPONSA

 

N-acetyl-gamma-calicheamicin dimethylhydrazide is a substrate of P‑glycoprotein (P-gp).

 

Effect of BESPONSA on Metabolic Pathways and Transporter Systems

 

At clinically relevant concentrations, N-acetyl-gamma-calicheamicin dimethylhydrazide had a low potential to:

·        Inhibit cytochrome P450 (CYP 450) Enzymes: CYP1A2, CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP2D6, and CYP3A4/5.

·        Induce CYP450 Enzymes: CYP1A2, CYP2B6, and CYP3A4.

·        Inhibit UGT Enzymes: UGT1A1, UGT1A4, UGT1A6, UGT1A9, and UGT2B7.

·        Inhibit Drug Transporters: P‑gp, breast cancer resistance protein (BCRP), organic anion transporter (OAT)1 and OAT3, organic cation transporter (OCT)2, and organic anion transporting polypeptide (OATP)1B1 and OATP1B3.

 

At clinically relevant concentrations, inotuzumab ozogamicin had a low potential to:

·        Inhibit CYP450 Enzymes: CYP1A2, CYP2A6, CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP2D6, and CYP3A4/5.

·        Induce CYP450 Enzymes: CYP1A2, CYP2B6, and CYP3A4.

 

NONCLINICAL TOXICOLOGY

 

Carcinogenesis, Mutagenesis, Impairment of Fertility

 

Formal carcinogenicity studies have not been conducted with inotuzumab ozogamicin. In toxicity studies, rats were dosed weekly for 4 or 26 weeks with inotuzumab ozogamicin at doses up to 4.1 mg/m² and 0.73 mg/m², respectively. After 26 weeks of dosing, rats developed hepatocellular adenomas in the liver at 0.73 mg/m² (approximately 2 times the exposure in patients at the maximum recommended dose, based on AUC).

 

Inotuzumab ozogamicin was clastogenic in vivo in the bone marrow of male mice that received single doses ≥1.1 mg/m². This is consistent with the known induction of DNA breaks by calicheamicin. N‑acetyl-gamma-calicheamicin dimethylhydrazide (the cytotoxic agent released from inotuzumab ozogamicin) was mutagenic in an in vitro bacterial reverse mutation (Ames) assay.

 

In a female fertility and early embryonic development study, female rats were administered daily intravenous doses of inotuzumab ozogamicin up to 0.11 mg/m² for 2 weeks before mating through Day 7 of pregnancy. An increase in the proportion of resorptions and decrease in the number of viable embryos and gravid uterine weights were observed at the 0.11 mg/m² dose level (approximately 2 times the exposure in patients at the maximum recommended dose, based on AUC). Additional findings in female reproductive organs occurred in repeat-dose toxicology studies and included decreased ovarian and uterine weights, and ovarian and uterine atrophy. Findings in male reproductive organs occurred in repeat-dose toxicology studies and included decreased testicular weights, testicular degeneration, hypospermia, and prostatic and seminal vesicle atrophy. Testicular degeneration and hypospermia were nonreversible following a 4‑week nondosing period. In the chronic studies of 26-weeks duration, adverse effects on reproductive organs occurred at ≥0.07 mg/m² in male rats and at 0.73 mg/m² in female monkeys [see 4.6 Fertility, Pregnancy and lactation ].

 

 

5.4 Clinical studies

 

 

Patients With Relapsed or Refractory ALL – INO-VATE ALL

 

The safety and efficacy of BESPONSA were evaluated in INO-VATE ALL (NCT01564784) a randomized (1:1), open‑label, international, multicenter study in patients with relapsed or refractory ALL. Patients were stratified at randomization based on duration of first remission (< 12 months or ≥ 12 months, salvage treatment (Salvage 1 or 2) and patient age at randomization (< 55 or ≥ 55 years). Eligible patients were ≥ 18 years of age with Philadelphia chromosome-negative or Philadelphia chromosome-positive relapsed or refractory B‑cell precursor ALL. All patients were required to have ≥ 5% bone marrow blasts and to have received 1 or 2 previous induction chemotherapy regimens for ALL. Patients with Philadelphia chromosome‑positive B‑cell precursor ALL were required to have disease that failed treatment with at least 1 tyrosine kinase inhibitor and standard chemotherapy. Table 1 shows the dosing regimen used to treat patients.

 

Among all 326 patients who were randomized to receive BESPONSA (N=164) or Investigator’s choice of chemotherapy (N=162), 215 patients (66%) had received 1 prior treatment regimen for ALL and 108 patients (33%) had received 2 prior treatment regimens for ALL. The median age was 47 years (range: 18‑79 years), 276 patients (85%) had Philadelphia chromosome‑negative ALL, 206 patients (63%) had a duration of first remission < 12 months, and 55 patients (17%) had undergone a HSCT prior to receiving BESPONSA or Investigator’s choice of chemotherapy. The two treatment groups were generally balanced with respect to the baseline demographics and disease characteristics.

 

All evaluable patients had B‑cell precursor ALL that expressed CD22, with ≥ 90% of evaluable patients exhibiting ≥ 70% leukemic blast CD22 positivity prior to treatment, as assessed by flow cytometry performed at a central laboratory.

 

The efficacy of BESPONSA was established on the basis of CR, the duration of CR, and proportion of MRD-negative CR (< 1 x 10^-4 of bone marrow nucleated cells by flow cytometry) in the first 218 patients randomized. CR, duration of remission (DoR), and MRD results in the initial 218 randomized patients were consistent with those seen in all 326 randomized patients.

 

Among the initial 218 randomized patients, 64/88 (73%) and 21/88 (24%) of responding patients per EAC achieved CR/CRi in Cycles 1 and 2, respectively, in the BESPONSA arm, and 29/32 (91%) and 1/32 (3%) of responding patients per EAC achieved a CR/CRi in Cycles 1 and 2, respectively, in the Investigator’s choice of chemotherapy arm.

 

Table 8 shows the efficacy results from this study.

 

Table 8.     Efficacy Results in Patients With Relapsed or Refractory B‑Cell Precursor ALL Who Received BESPONSA or Investigator’s Choice of Chemotherapy (FLAG, MXN/Ara‑C, or HIDAC)
	CRa			CRib			CR/CRia,b
	BESPONSA (N=109)		HIDAC, FLAG, or MXN/Ara-C (N=109)	BESPONSA (N=109)		HIDAC, FLAG or MXN/Ara-C (N=109)	BESPONSA (N=109)	HIDAC, FLAG, or MXN/Ara-C (N=109)
Responding (CR/CRi) patients
n (%) [95% CI]	39 (35.8) [26.8-45.5]		19 (17.4) [10.8-25.9]	49 (45.0) [35.4-54.8]		13 (11.9) [6.5-19.5]	88 (80.7) [72.1-87.7]	32 (29.4) [21.0-38.8]
p-valuec							<0.0001
DoRd
n	39	18		45	14		84		32
Median, months [95% CI]	8.0 [4.9-10.4]	4.9 [2.9-7.2]		4.6 [3.7-5.7]	2.9 [0.6-5.7]		5.4 [4.2-8.0]		3.5 [2.9-6.6]
MRD-negativitye
n	35	6		34	3		69		9
Ratef (%) [95% CI]	35/39 (89.7) [75.8-97.1]	6/19 (31.6) [12.6-56.6]		34/49 (69.4) [54.6-81.7]	3/13 (23.1) [5.0-53.8]		69/88 (78.4) [68.4-86.5]		9/32 (28.1) [13.7-46.7]
Abbreviations: CI=confidence interval; CR=complete remission; CRi=complete remission with incomplete hematologic recovery; DoR=duration of remission; EAC=Endpoint Adjudication Committee; FLAG=fludarabine + cytarabine + granulocyte colony-stimulating factor; HIDAC=high-dose cytarabine; HR=hazard ratio; MRD=minimal residual disease; MXN/AraC=mitoxantrone + cytarabine; N/n=number of patients; OS=overall survival; PFS=progression-free survival.
a     CR, per EAC, was defined as < 5% blasts in the bone marrow and the absence of peripheral blood leukemic blasts, full recovery of peripheral blood counts (platelets ≥ 100 × 109/L and absolute neutrophil counts [ANC] ≥ 1 × 109/L) and resolution of any extramedullary disease. b     CRi, per EAC, was defined as < 5% blasts in the bone marrow and the absence of peripheral blood leukemic blasts, incomplete recovery of peripheral blood counts (platelets < 100 × 109/L and/or ANC < 1 × 109/L) and resolution of any extramedullary disease. c     1-sided p-value using Chi-squared test. d     DoR, based on a later cutoff date than the CR/CRi, was defined for patients who achieved CR/CRi per Investigator’s assessment as time since first response of CRa or CRib per Investigator’s assessment to the date of a PFS event or censoring date if no PFS event was documented.  e    MRD-negativity was defined by flow cytometry as leukemic cells comprising < 1 × 10-4 (< 0.01%) of bone marrow nucleated cells. f     Rate was defined as the number of patients who achieved MRD negativity divided by the total number of patients who achieved CR/CRi per EAC.

 

Among the initial 218 patients, as per EAC assessment, 32/109 patients (29%) in the BESPONSA arm achieved complete remission with partial hematologic recovery (CRh; defined as <5% blasts in the bone marrow, ANC > 0.5 x 10⁹/L, and platelet counts > 50 x 10⁹/L but not meeting full recovery of peripheral blood counts) versus 6/109 patients (6%) in the Investigator’s choice of chemotherapy arm, and 71/109 patients (65%) in the BESPONSA arm achieved CR/CRh versus 25/109 patients (23%) in the Investigator’s choice of chemotherapy arm.

 

Overall, 79/164 patients (48%) in the BESPONSA arm and 35/162 patients (22%) in the Investigator’s choice of chemotherapy arm had a follow-up HSCT.

 

Figure 1 shows the analysis of overall survival (OS). The analysis of OS did not meet the pre-specified boundary for statistical significance.

 

Tromethamine (Trometamol) 10mg/vial, Sucrose 200mg/vial, Polysorbate 80 0.4mg/vial & Sodium Chloride 2.4mg/vial.

Not applicable

Shelf life : 3 years Instructions for Reconstitution, Dilution, and Administration Protect the reconstituted and diluted BESPONSA solutions from light. Do not freeze the reconstituted or diluted solution. The maximum time from reconstitution through the end of administration should be less than or equal to 8 hours, with less than or equal to 4 hours between reconstitution and dilution. Reconstitution: • BESPONSA is a cytotoxic drug. Follow applicable special handling and disposal procedures.1 • Calculate the dose (mg) and number of vials of BESPONSA required. • Reconstitute each vial with 4 mL of Sterile Water for Injection, USP, to obtain a concentration of 0.25 mg/mL of BESPONSA that delivers 3.6 mL (0.9 mg). • Gently swirl the vial to aid dissolution. DO NOT SHAKE. • Inspect the reconstituted solution for particulates and discoloration. The reconstituted solution should be clear to opalescent, colorless to slightly yellow, and essentially free of visible foreign matter. • See Table 5 for storage times and conditions for the reconstituted solution. Dilution: • Calculate the required volume of the reconstituted solution needed to obtain the appropriate dose according to the patient’s body surface area. Withdraw this amount from the vial(s) using a syringe. Discard any unused reconstituted BESPONSA solution left in the vial. • Add reconstituted solution to an infusion container with 0.9% Sodium Chloride Injection, USP, to a make a total volume of 50 mL. An infusion container made of polyvinyl chloride (PVC) (di(2 ethylhexyl)phthalate [DEHP]- or non-DEHP-containing), polyolefin (polypropylene and/or polyethylene), or ethylene vinyl acetate (EVA) is recommended. • Gently invert the infusion container to mix the diluted solution. DO NOT SHAKE. • See Table 5 for storage times and conditions for the diluted solution. Administration: • See Table 5 for storage times and conditions for prior to and during administration of the diluted solution. • Filtration of the diluted solution is not required. However, if the diluted solution is filtered, polyethersulfone (PES)-, polyvinylidene fluoride (PVDF) ,or hydrophilic polysulfone (HPS) based filters are recommended. Do not use filters made of nylon or mixed cellulose ester (MCE). • Infuse the diluted solution for 1 hour at a rate of 50 mL/h at room temperature (20 25°C; 68 77°F). Infusion lines made of PVC (DEHP or non DEHP containing), polyolefin (polypropylene and/or polyethylene), or polybutadiene are recommended. Do not mix BESPONSA or administer as an infusion with other medicinal products. Table 5 shows the storage times and conditions for reconstitution, dilution, and administration of BESPONSA. Table 5. Storage Times and Conditions for Reconstituted and Diluted BESPONSA Solution Maximum time from reconstitution through end of administration less than or equal to 8 hoursa Reconstituted Solution Diluted Solution After Start of Dilution Administration BESPONSA contains no bacteriostatic preservatives. Use reconstituted solution immediately or after being refrigerated (2 8°C; 36 46°F) for up to 4 hours. PROTECT FROM LIGHT. DO NOT FREEZE. Use diluted solution immediately or after storage at room temperature (20 25°C; 68-77°F) for up to 4 hours or being refrigerated (2 8°C; 36 46°F) for up to 3 hours. PROTECT FROM LIGHT. DO NOT FREEZE. If the diluted solution is refrigerated (2 8°C; 36 46°F), allow it to equilibrate at room temperature (20 25°C; 68 77°F) for approximately 1 hour prior to administration. Administer diluted solution within 8 hours of reconstitution as a 1 hour infusion at a rate of 50 mL/h at room temperature (20 25°C; 68 77°F). PROTECT FROM LIGHT. a With less than or equal to 4 hours between reconstitution and dilution. Protect the reconstituted and diluted BESPONSA solutions from light. Do not freeze the reconstituted or diluted solution. The maximum time from reconstitution through the end of administration should be less than or equal to 8 hours, with less than or equal to 4 hours between reconstitution and dilution. Do not use Besponsa after the expiry date which is stated on the Vial label after EXP:. The expiry date refers to the last day of that month.

Keep out of the sight and reach of children.

 

 

 

Refrigerate (2‑8°C) BESPONSA vials and store in the original carton to protect from light. Do not freeze.

 

BESPONSA is a cytotoxic drug. Follow applicable special handling and disposal procedures.¹

 

BESPONSA (inotuzumab ozogamicin) for Injection is supplied as a white to off-white lyophilized powder in a single-dose amber Type I glass tubing vials with chlorobutyl lyophylization stoppers and crimp seals with flip-off caps for reconstitution and further dilution. Each vial delivers 0.9 mg inotuzumab ozogamicin. Each carton contains one single‑dose vial.

 

 

BESPONSA is a cytotoxic drug. Follow applicable special handling and disposal procedures.