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SUMMARY OF PRODUCT CHARACTERISTICS
NAME OF THE MEDICINAL PRODUCT
Zevalin 1.6 mg/ml kit for radiopharmaceutical preparations for infusion 2. QUALITATIVE
QUANTITATIVE
COMPOSITION
Zevalin is supplied as a kit for the preparation of yttrium-90 radiolabelled ibritumomab tiuxetan. The kit contains one ibritumomab tiuxetan vial, one sodium acetate vial, one formulation buffer vial, and one empty reaction vial. One ibritumomab tiuxetan vial contains 3.2 mg ibritumomab tiuxetan* in 2 ml solution (1.6 mg per ml). *murine IgG1 monoclonal antibody produced by recombinant DNA technology in a Chinese hamster ovary (CHO) cell line and conjugated to the chelating agent MX-DTPA. The final formulation after radiolabelling contains 2.08 mg ibritumomab tiuxetan [90Y] in a total volume of 10 ml. Excipients This medicinal product can contain up to 28 mg sodium per dose, depending on the radioactivity concentration. To be taken into consideration by patients on a controlled sodium diet. For a full list of excipients, see section 6.1. 3. PHARMACEUTICAL
Kit for radiopharmaceutical preparations for infusion. Ibritumomab tiuxetan vial: Clear colourless solution. Sodium acetate vial: Clear colourless solution. Formulation buffer vial: Clear colourless solution. 4. CLINICAL
PARTICULARS

4.1 Therapeutic
indications

[90Y]-radiolabelled Zevalin is indicated as consolidation therapy after remission induction in
previously untreated patients with follicular lymphoma. The benefit of Zevalin following rituximab in
combination with chemotherapy has not been established.
[90Y]-radiolabelled Zevalin is indicated for the treatment of adult patients with rituximab relapsed or
refractory CD20+ follicular B-cell non-Hodgkin's lymphoma (NHL).
4.2
Posology and method of administration

[90Y]-radiolabelled Zevalin must only be received, handled and administered by qualified personnel
and must be prepared in accordance with both radiation safety and pharmaceutical quality
requirements (for more details see also sections 4.4, 6.6 and 12).
Posology Zevalin must be used following pretreatment with rituximab. Please refer to the Summary of Product Characteristics of rituximab for detailed guidance on its use. The treatment regimen consists of two intravenous administrations of rituximab and one administration of [90Y]-radiolabelled Zevalin solution in the following order: Day 1: intravenous infusion of 250 mg/m2 rituximab. intravenous infusion of 250 mg/m2 rituximab shortly (within 4 hours) before administration of [90Y]-radiolabelled Zevalin solution. 10-minute intravenous infusion of [90Y]-radiolabelled Zevalin solution. Repeated use: Data on the re-treatment of patients with Zevalin are not available. The recommended radioactivity dose of [90Y]-radiolabelled Zevalin solution is: Treatment of rituximab relapsed or refractory CD20+ follicular B-cell non-Hodgkin's lymphoma (NHL): - patients ≥ 150,000 platelets/mm3: 15 MBq/kg body weight. patients with 100,000-150,000 platelets/mm3: 11 MBq/kg The maximum dose must not exceed 1200 MBq. Repeated use: Data on the re-treatment of patients with [90Y]-radiolabeled Zevalin are not available. Consolidation therapy after remission induction in previously untreated patients with follicular lymphoma - patients with ≥ 150,000 platelets/mm³: 15 MBq/kg up to a maximum of 1200 MBq. - For patients with less than 150,000 platelets per mm³ see section ‘4.4’ Repeated use: Data on the re-treatment of patients with [90Y]-radiolabelled Zevalin are not available. Special populations  Zevalin is not recommended for use in children and adolescents below 18 years due to a lack of data on safety and efficacy. Limited data in elderly patients (aged ≥ 65 years) are available. No overall differences in safety or efficacy were observed between these patients and younger patients. The safety and efficacy have not been studied in patients with hepatic impairment. The safety and efficacy have not been studied in patients with renal impairment. Method of administration The [90Y]-radiolabelled Zevalin solution must be prepared according to section 12. Before administration to the patient, the percent radioincorporation of the prepared [90Y]-radiolabelled
Zevalin must be checked according to the procedure outlined in section 12.
If the average radiochemical purity is less than 95%, the preparation must not be administered.
The prepared solution must be given as a slow intravenous infusion over 10 minutes.
The infusion must not be administered as an intravenous bolus.
Zevalin may be infused directly by stopping the flow from an infusion bag and administering it
directly into the line. A 0.2 or 0.22 micron low protein-binding filter must be on line between the
patient and the infusion port. The line must be flushed with at least 10 ml of sodium chloride 9 mg/ml
(0.9%) solution for injection after the infusion of Zevalin.
4.3 Contraindications
-
Hypersensitivity to ibritumomab tiuxetan, to yttrium chloride, or to any of the excipients. Hypersensitivity to rituximab or to other murine-derived proteins Pregnancy and lactation (see section 4.6). Special warnings and precautions for use
Since the Zevalin regimen includes rituximab, see also the Summary of Product Characteristics of rituximab. [90Y]-radiolabelled Zevalin solution must only be received, handled and administered by qualified personnel with the appropriate government authorization for the use and manipulation of radionuclides within a designated clinical setting. Its receipt, preparation, use, transfer, storage, and disposal are subject to the regulations and/or appropriate authorisation/licences of the local competent official organisations. Radiopharmaceuticals must be prepared by the user in a manner which satisfies both radiation safety and pharmaceutical quality requirements. Appropriate aseptic precautions must be taken, complying with the requirements of Good Manufacturing Practice of pharmaceuticals. Infusions must be administered under the close supervision of an experienced physician with full resuscitation facilities immediately available (for radiopharmaceutical precautions see also sections ‘4.2 and 12’). [90Y]-radiolabelled Zevalin solution must not be administered to patients who are likely to develop life-threatening haematological toxicity signs. Zevalin must not be administered in patients mentioned below, as safety and efficacy have not been established: - > 25% of the bone marrow infiltrated by lymphoma cells - prior external beam radiation affecting more than 25% of active bone marrow - platelet <100,000/mm3 (monotherapy) and <150,000/mm3 (consolidation treatment) - neutrophil counts < 1,500/mm3 - prior bone marrow transplant or stem cell support Haematological toxicity Special caution is required with respect to bone marrow depletion. In most patients, administration of Zevalin (after pretreatment with rituximab) results in severe and prolonged cytopenia which is generally reversible (see section 4.8). Therefore, complete blood cell and platelet counts must be monitored following Zevalin treatment weekly until levels recover or as clinically indicated. The risk of haematological toxicity may be increased after prior therapy with fludarabine containing regimens (for details see section 4.5).  Treatment with growth factors Patients must not receive growth factor treatment such as G-CSF for 3 weeks prior to Zevalin administration as well as for 2 weeks following completion of the treatment in order to assess the adequate bone marrow reserve correctly and because of the potential sensitivity of rapidly dividing myeloid cells to radiation (see also section 4.5).  Patients who had received murine-derived proteins before Zevalin treatment must be tested for human anti-murine antibodies (HAMA). Patients who have developed HAMAs may have allergic or hypersensitivity reactions when treated with Zevalin or other murine-derived proteins. After use of Zevalin, patients must generally be tested for HAMA before any further treatment with murine-derived proteins.  Infusion reactions Infusion reactions may occur during or following Zevalin administration after pretreatment with Rituximab. Signs and symptoms of infusion reactions may include dizziness, cough, nausea, vomiting, rash, pruritus, tachycardia, asthenia, pyrexia and rigors (see section 4.8). In case of a potential severe infusion reaction treatment must be stopped immediately.  Hypersensitivity reactions following Zevalin administration are commonly observed. Severe hypersensitivity reactions including anaphylaxis occur in < 1 % of patients (see also section 4.8). In case of hypersensitivity reactions, Zevalin infusion must be stopped immediately. Medicinal products for the treatment of hypersensitivity reactions, e.g. adrenaline, antihistamines and corticosteroids, must be available for immediate use in the event of an allergic reaction during administration of rituximab or Zevalin.  Severe mucocutaneous reactions, including Stevens-Johnson Syndrome, some with fatal outcome, have been reported in association with Zevalin after pretreatment with rituximab. The onset of the reactions varied from days to months. In patients experiencing a severe mucocutaneous reaction treatment must be discontinued. 
Long-term animal studies on the effect on fertility and reproductive function have not been performed.
There is a potential risk that ionizing radiation by [90Y]-radiolabelled Zevalin could cause toxic effects
on female and male gonads. Due to the nature of the compound, women of child-bearing potential, as
well as males, must use effective contraceptive methods during and up to 12 months after treatment
with Zevalin (see also section 4.6 and 5.2).
 Immunization
The safety and efficacy of immunization with any vaccine, particularly live viral vaccines, following
therapy with Zevalin have not been studied. Due to the potential risk of developing viral infections it
is not recommended to administer live viral vaccines to patients who have recently received Zevalin
(see section 4.5). A potentially limited ability to generate a primary or anamnestic humoral response to
any vaccine following Zevalin treatment has to be taken into consideration.

 NHL with CNS involvement
No data are available on patients with CNS-lymphoma as those patients were not included in clinical
studies. The use of Zevalin is therefore not recommended in NHL patients with CNS involvement.
 Extravasation
Close monitoring for evidence of extravasation during the injection of Zevalin is required in order to
avoid radiation-associated tissue damage. If any signs or symptoms of extravasation have occurred, the
infusion must be immediately terminated and restarted in another vein.
 Excipients
The final [90Y]-radiolabelled Zevalin solution contains up to 28 mg sodium per dose, depending on the
radioactivity concentration. Patients on a controlled sodium diet must take this into consideration.
4.5
Interaction with other medicinal products and other forms of interaction

There are no known interactions with other medicinal products. No interaction studies have been
performed.
Growth factor treatment such as G-CSF must not be given to patients for 3 weeks prior to Zevalin
administration as well as for 2 weeks following completion of the treatment (see also section 4.4).
In a clinical trial in which Zevalin was administered as consolidation after prior first line
chemotherapy, a higher frequency of severe and prolonged neutropenia and thrombocytopenia was
observed in patients who had received Zevalin within 4 months after a combination chemotherapy of
fludarabine with mitoxantrone and/or cyclophosphamide compared to those patients who had received
any other chemotherapy. Hence the risk of haematological toxicity may be increased when Zevalin is
administered shortly (< 4 months) after fludarabine-containing regimens (see also section 4.4).
The safety and efficacy of immunization with any vaccine, particularly live viral vaccines, following
therapy with Zevalin have not been studied (see also section ‘Special warnings and precautions for
use’).
4.6
Pregnancy and lactation

Pregnancy
Animal reproduction studies were not conducted with ibritumomab tiuxetan. Since IgGs are known to
cross the placenta, and because of the significant risk associated with radiation, Zevalin is
contraindicated during pregnancy (see section 4.3).
Pregnancy must be excluded before the start of treatment in women.
Any woman who has missed a period must be assumed to be pregnant until proven otherwise and
alternative therapies which do not involve ionising radiation must be then considered.
Women of childbearing potential as well as males must use effective contraceptive methods during
and up to 12 months after treatment with Zevalin.
Lactation
Although it is not known whether ibritumomab tiuxetan is excreted in human milk, maternal IgGs are
known to be excreted in human milk. Therefore, women must discontinue breast-feeding, as the
potential for absorption and immunosuppression in the infant is unknown. Zevalin must be used
following pretreatment with rituximab for which breast-feeding is not recommended during treatment
and up to 12 months following treatment (please refer to the Summary of Product Characteristics of
rituximab for detailed guidance on its use).
Fertility
No animal studies have been performed to determine the effects of Zevalin on fertility in males or
females. There is a potential risk that ionizing radiation by [90Y]-radiolabelled Zevalin could cause
toxic effects on female and male gonads (see sections ‘4.4 and 5.2). Patients should be advised that
fertility may be affected and that male patients may wish to consider semen cryopreservation.
4.7
Effects on ability to drive and use machines

Zevalin could affect the ability to drive and to use machines, as dizziness has been reported as a
common side effect.
4.8 Undesirable
The radiation dose resulting from therapeutic exposure may result in secondary malignancies and in development of hereditary defects. It is necessary to ensure that the risks of the radiation are less than from the disease itself. Since Zevalin is used after pretreatment with rituximab (for details see section 4.2), see also the prescribing information of rituximab. The overall safety profile of Zevalin after pretreatment with rituximab is based on data from 349 patients with relapsed or refractory low-grade, follicular, or transformed B-cell non-Hodgkin’s lymphoma studied in five clinical trials, on data from a study with 204 patients receiving Zevalin as consolidation therapy after first-line remission induction, and from post-marketing surveillance. The most frequently observed adverse drug reactions in patients receiving Zevalin after pretreatment with rituximab are thrombocytopenia, leukocytopenia, neutropenia, anaemia, infections, pyrexia, nausea, asthenia, rigors, petechiae, and fatigue. The most serious adverse drug reactions in patients receiving Zevalin after pretreatment with rituximab are:  Severe and prolonged cytopenias (see also ‘Special warnings and precautions for use’)  Infections  Haemorrhage while thrombocytopenic  Severe mucocutaneous reactions (see also ‘Special warnings and precautions for use’)  Myelodysplastic syndrome / acute myeloid leukaemia Fatal outcomes have been reported for each of the following serious adverse drug reactions. These reports originated either from clinical trials or from postmarking experience.  Infection  Sepsis  Pneumonia  Myelodysplastic syndrome / Acute myeloid leukaemia  Anaemia  Pancytopenia  Haemorrhage while thrombocytopenic  Intracranial haemorrhage while thrombocytopenic  Mucocutaneous reactions, including Stevens-Johnson Syndrome The frequencies of the adverse drug reactions which were considered to be at least possibly related to Zevalin after pretreatment with rituximab are represented in the table below. These adverse drug reactions are based upon 349 patients with relapsed or refractory low-grade, follicular, or transformed B-cell non-Hodgkin’s lymphoma studied in 5 clinical trials. In addition, the adverse drug reactions marked with ** were observed in the study with 204 patients receiving Zevalin as consolidation therapy after first-line remission induction where indicated. The adverse drug reactions identified only during post-marketing surveillance, and for which a frequency could not be estimated, are listed under „not known“. Adverse reactions listed below are classified according to frequency and System Organ Class (MedDRA). Frequency groupings are defined according to the following convention: (very common ≥1/10, common ≥1/100 to <1/10, uncommon ≥ 1/1,000 to 1/100, rare:  1/10,000 to <1/1,000; very rare: <1/10,000). Within each frequency grouping, undesirable effects are presented in order of decreasing seriousness. Table 1: Adverse drug reactions reported in clinical trials or during post-marketing surveillance in patients treated with Zevalin after pretreatment with rituximab System Organ Class
Very common
Uncommon
Not known
(MedDRA)
Infections and
infestations
Sepsis*, Pneumonia*, Urinary tract infection, Oral candidiasis Neoplasms benign,
malignant and
unspecified (incl cysts
and polyps)
Blood and lymphatic Thrombocytopenia, Febrile neutropenia,
system disorders
Immune system
disorders
Metabolism and
nutrition disorders
Psychiatric disorders Anxiety,
Nervous system
disorders
Cardiac disorders
Vascular disorders
Respiratory, thoracic, Cough,
and mediastinal
disorders
Gastrointestinal
disorders
Abdominal pain, Diarrhoea, Dyspepsia, Throat irritation, Constipation System Organ Class
Very common
Uncommon
Not known
(MedDRA)
Reproductive system Amenorrhea**
and breast disorders
Skin and
subcutaneous tissue
disorders
Musculoskeletal and
connective tissue
disorders
General disorders and Asthenia,
administration site
conditions
Damage to lymphoma-surrounding tissue and complications due to lymphoma swelling * fatal outcome has been observed ** has been observed in a study with 204 patients receiving Zevalin as consolidation after first-line remission induction The most appropriate MedDRA term is used to describe a certain reaction and its synonyms and related conditions.  Blood and lymphatic system disorders Haematological toxicity has been very commonly observed in clinical trials, and is dose-limiting (see also section ‘Special warnings and precautions for use’). Median time to blood platelet and granulocyte nadirs were around 60 days after start of treatment. In clinical trials with the indication of relapsed and refractory NHL, grade 3 or 4 thrombocytopenia was reported with median times to recovery of 13 and 21 days and grade 3 or 4 neutropenia with median times to recovery of 8 and 14 days. Following Zevalin as consolidation after first line remission induction the median times to recovery was 20 days and 35 days for grade 3 or 4 thrombocytopenia and 20 days and 28 days for grade 3 or 4 neutropenia. - Data from 349 patients with relapsed or refractory low-grade, follicular lymphoma, or transformed non-Hodgkin’s lymphoma studied in five trials:
During the first 13 weeks after treatment with Zevalin, patients very commonly developed
infections. Grade 3 and grade 4 infections were reported commonly. During follow-up,
infections occurred commonly. Of these, grade 3 was common, grade 4 uncommon.
- Data from 204 patients receiving Zevalin as consolidation therapy after first line remission induction: Infections were very commonly observed. Infections may be bacterial, fungal, viral including reactivation of latent viruses.  General disorders and administration site conditions Reports of extravasation with subsequent infusion site reactions including e.g. infusion site dermatitis, infusion site desquamation, and infusion site ulcer have been received. Zevalin-associated radiation might cause damage to lymphoma-surrounding tissue and complications due to lymphoma swelling Data from 349 patients with relapsed or refractory low-grade, follicular lymphoma, or transformed non-Hodgkin’s lymphoma studied in five trials: Hypersensitivity reactions following Zevalin administration are commonly observed. Severe (Grade 3/4) hypersensitivity reactions including anaphylaxis occur in less than 1% of patients (see also section ‘Special warnings and precautions for use’).  Neoplasms benign, malignant and unspecified (incl cysts and polyps) Myelodysplastic syndrome (MDS)/ acute myeloid leukaemia (AML) has been reported in five out of 211 patients assigned to treatment with Zevalin. The risk of developing secondary myelodysplasia or leukaemia following therapy with alkylating agents is well known. Since all of these patients had previously received treatment regimens including alkylating agents, available results provide insufficient data on whether Zevalin contributes to an increased risk of MDS/AML, or on the extent of risk.
4.9 Overdose
Doses up to 19.2 MBq/kg of Zevalin have been administered in clinical trials. Expected
haematological toxicity was observed, including grade 3 or 4. Patients recovered from these toxicity
signs, and overdoses were not associated with serious or fatal outcome.
There is no known specific antidote for [90Y]-radiolabelled Zevalin overdosage. Treatment consists of
discontinuation of Zevalin and supportive therapy, which may include growth factors. If available,
autologous stem cell support must be administered to manage haematological toxicity.
5. PHARMACOLOGICAL
PROPERTIES

5.1 Pharmacodynamic
properties
Pharmacotherapeutic group: Various therapeutic radiopharmaceuticals, ATC code: V10XX02  Ibritumomab tiuxetan is a recombinant murine IgG1 kappa monoclonal antibody specific for the B-cell antigen CD20. Ibritumomab tiuxetan targets the antigen CD20 which is located on the surface of malignant and normal B-lymphocytes. During B-cell maturation, CD20 is first expressed in the midstage of B-lymphoblast (pre-B-cell), and is lost during the final stage of B-cell maturation to plasma cells. It is not shed from the cell surface and does not internalise on antibody binding. [90Y]-radiolabelled ibritumomab tiuxetan binds specifically to CD20-expressing B-cells, including malignant cells. The isotope yttrium-90 is a pure β-emitter and has a mean path length of about 5 mm. This results in the ability to kill both targeted and neighbouring cells. The conjugated antibody has an apparent affinity constant for the CD20 antigen of approximately 17 nM. The binding pattern is very restricted, with no cross-reactivity to other leukocytes or to other types of human tissue. Rituximab pretreatment is necessary to clear circulating B-cells, enabling ibritumomab tiuxetan [90Y] to deliver radiation more specifically to the lymphoma B-cells. Rituximab is administered in a reduced dose when compared with the approved monotherapy. Treatment with [90Y]-radiolabelled Zevalin also leads to depletion of normal CD20+ B-cells. Pharmacodynamic analysis demonstrated that this was a temporary effect; recovery of normal B-cells began within 6 months and median counts of B-cells were within normal range within 9 months after treatment.  The safety and efficacy of the Zevalin therapeutic regimen were evaluated in two multi-center trials enrolling a total of 197 subjects. The Zevalin therapeutic regimen was administered in two steps (see 4.2). The efficacy and safety of a variation of the Zevalin therapeutic regimen employing a reduced dose of ibritumomab tiuxetan [90Y] was further defined in a third study enrolling a total of 30 patients who had mild thrombocytopenia (platelet count 100,000 to 149,000 cells/mm3). Study 1 was a single-arm study of 54 patients with relapsed follicular lymphoma refractory to rituximab treatment. Patients were considered refractory if their last prior treatment with rituximab did not result in a complete or partial response, or if time to disease progression (TTP) was  6 months. The primary efficacy endpoint of the study was the overall response rate (ORR) using the International Workshop Response Criteria (IWRC). Secondary efficacy endpoints included time to disease progression (TTP) and duration of response (DR). In a secondary analysis comparing objective response to the Zevalin therapeutic regimen with that observed with the most recent treatment with rituximab, the median duration of response following the Zevalin therapeutic regimen was 6 vs. 4 months. Table 1 summarizes efficacy data from this study. Study 2 was a randomized, controlled, multicenter study comparing the Zevalin therapeutic regimen versus treatment with rituximab. The trial was conducted in 143 rituximab-naïve patients with relapsed or refractory low-grade or follicular non-Hodgkin's lymphoma (NHL), or transformed B-cell NHL. A total of 73 patients received the Zevalin therapeutic regimen, and 70 patients received rituximab given as an intravenous infusion at 375 mg/m2 weekly times 4 doses. The primary efficacy endpoint of the study was to determine the ORR using the IWRC (see Table 2). The ORR was significantly higher (80% vs. 56%, p = 0.002) for patients treated with the Zevalin therapeutic regimen. The secondary endpoints, duration of response and time to progression, were not significantly different between the two treatment arms. Table 2.Summary of Efficacy Data in patients with relapsed/refractory low-grade or
follicular non-Hodgkin's lymphoma (NHL), or transformed B-cell NHL
Rituximab
therapeutic
therapeutic
1IWRC: International Workshop response criteria 4Duration of response: interval from the onset of response to disease progression. 6Time to Disease Progression: interval from the first infusion to disease progression. Study 3 was a single arm study of 30 patients with relapsed or refractory low-grade, follicular, or transformed B-cell NHL who had mild thrombocytopenia (platelet count 100,000 to 149,000 cells/mm3). Excluded from the study were patients with 25% lymphoma marrow involvement and/or impaired bone marrow reserve. Patients were considered to have impaired bone marrow reserve if they had any of the following: prior myeloablative therapy with stem cell support; prior external beam radiation to >25% of active marrow; a platelet count <100,000 cells/mm3; or neutrophil count <1,500 cells/mm3. In this study, a modification of the Zevalin therapeutic regimen with a lower [90Y]-Zevalin activity per body weight (11 MBq/kg) was used. Objective, durable clinical responses were observed [67% ORR (95% CI: 48-85%), 11.8 months median DR (range: 4-17 months)] and resulted in a greater incidence of haematologic toxicity (see 4.8) than in Studies 1 and 2. Study 4 investigated the efficacy and safety of Zevalin consolidation in patients with advanced-stage follicular lymphoma responding to first-line chemotherapy. Major inclusion criteria were: CD20+ grade 1 or 2 follicular lymphoma; stage III or IV at diagnosis; normal peripheral blood cell counts; < 25% bone marrow involvement; age ≥ 18 yrs; and complete response (CR/Cru) or partial response (PR) after first-line chemotherapy determined by physical examination, CT scans and bone marrow biopsy. After completing induction therapy, patients were randomized to receive either Zevalin (250 mg/m2 rituximab on day -7 and on day 0 followed on day 0 by Zevalin 15 MBq/kg body weight; maximal dose 1200 MBq; [n=208]) or no further treatment (control; n=206). Induction therapies included CVP n=106, CHOP (-like) n=188, fludarabine combinations n=22, chlorambucil n=39 and rituximab-chemotherapy combinations n=59. With a median follow-up of 2.9 years, the median progression free survival (PFS) increased from 13.5 months (control) to 37 months (Zevalin; p<0.0001; HR 0.465). For patient subgroups in PR or CR after induction, median PFS was 6.3 vs 29.7 months (p<0.0001; HR 0.304) and 29.9 vs 54.6 months (p=0.015; HR 0.613), respectively. After Zevalin consolidation, 77% of patients in PR after induction therapy converted to CR. Patients whose response status changed after Zevalin from PR to CR showed a significantly longer median progression free survival time (986 days) compared to those patients who remained in PR (median progression free survival
time of 460 days, p=0.0004). In total, 87% of patients were in CR(u); 76% in CR and 11% in CRu.
5.2 Pharmacokinetic
properties

In patients given intravenous infusions of 250 mg/m2 rituximab followed by intravenous injections of
15 MBq/kg of [90Y]-radiolabelled Zevalin, the median serum effective half-life of ibritumomab
tiuxetan [90Y] was 28 h.

As 90Y forms a stable complex with ibritumomab tiuxetan, the biodistribution of the radiolabel follows
the biodistribution of the antibody. Irradiation by the emitted beta particles from 90Y occurs in a radius
of 5 mm around the isotope.
In clinical studies, the [90Y]-radiolabelled Zevalin after pretreatment with rituximab results in a
significant radiation dose to the testes. The radiation dose to the ovaries has not been established.
There is a potential risk that [90Y]-radiolabelled Zevalin after pretreatment with rituximab could cause
toxic effects on the male and female gonads (see sections 4.4 and 4.6).
5.3 Preclinical
Non-clinical data reveal no special hazard for humans based on studies of single and repeated dose toxicity. The human radiation dose estimates derived from biodistribution studies in mice with [90Y]- or [111In]-radiolabelled ibritumomab tiuxetan predicted acceptable radiation to normal human tissue with limited levels of skeleton and bone marrow radiation. The linker chelate tiuxetan forms a stable complex with the radioisotopes yttrium-90 and indium-111 and only negligible degradation due to radiolysis is expected. The single and repeated dose toxicity studies of the non-radioactive compound in cynomolgus monkeys did not indicate any other risk than the expected B-cell depletion arising from the use of ibritumomab tiuxetan alone or in combination with rituximab. Studies on reproductive and developmental toxicity have not been performed. Studies on the mutagenic and carcinogenic potential of Zevalin have not been performed. Due to the exposure to ionising radiation derived from the radiolabel, a risk of mutagenic and carcinogenic effects has to be taken into account. 6. PHARMACEUTICAL
PARTICULARS
List of excipients
Sodium acetate Water for injections Disodium phosphate dodecahydrate Human albumin solution Hydrochloric acid, diluted (for pH adjustment) Pentetic acid
Potassium chloride
Potassium dihydrogen phosphate
Sodium chloride
Sodium hydroxide
Water for injections
6.2 Incompatibilities
This medicinal product must not be mixed with other medicinal products except those mentioned in
section 12.
No incompatibilities have been observed between Zevalin and infusion sets.
6.3 Shelf

5 years.
After radiolabelling, an immediate use is recommended. Chemical and physical in-use stability has
been demonstrated for 8 hours at 2°C - 8°C and protected from light.
6.4
Special precautions for storage

Store in a refrigerator (2C – 8C). Do not freeze.
Store the vials in the original package in order to protect from light.
Storage must be in accordance with local requirements for radioactive materials.
For storage conditions of the radiolabelled product, see section 6.3.
6.5
Nature and contents of container

Zevalin is supplied as a kit for the preparation of yttrium-90 (90Y) radiolabelled ibritumomab tiuxetan.
Zevalin contains 1 of each of the following:

Ibritumomab tiuxetan vial: type I glass vial with a rubber stopper (teflon-lined bromobutyl) containing
2 ml solution.
Sodium acetate vial: type I glass vial with a rubber stopper (teflon-lined bromobutyl) containing 2 ml
solution.
Formulation buffer vial: type I glass vial with a rubber stopper (teflon-lined bromobutyl) containing
10 ml solution.

Reaction vial: type I glass vial with a rubber stopper (teflon-lined bromobutyl)
Pack size of 1 kit.
6.6
Special precautions for disposal

Any unused product or waste material must be disposed of in accordance with local requirements.
Contaminated materials must be disposed of as radioactive waste by the authorised route.

Spectrum Pharmaceuticals B.V. Prins Bernhardplein 200 1097 JB Amsterdam The Netherlands MARKETING AUTHORISATION NUMBER

EU/1/03/264/001
DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
Date of first authorisation: 16 January 2004 Date of latest renewal: 16 January 2009 DATE OF REVISION OF THE TEXT
11. DOSIMETRY

Yttrium-90 decays by the emission of high-energy beta particles, with a physical half-life of
64.1 hours (2.67 days). The product of radioactive decay is stable zirconium-90. The path length of
beta emission (90) by yttrium-90 in tissue is 5 mm.
Analyses of estimated radiation absorbed dose were carried out using quantitative imaging with the
gamma-emitter [111In]-radiolabelled Zevalin, blood sampling, and the MIRDOSE3 software program.
The imaging dose of [111In]-radiolabelled Zevalin was always given immediately following an infusion
with rituximab at 250 mg/m² to deplete peripheral CD20+ cells and to optimise bio-distribution.
Following administration of [111In]-radiolabelled Zevalin, whole body scans were performed at up to
eight time-points, acquiring both anterior and posterior images. Blood samples, used to calculate
residence times for red marrow, were drawn up to eight time-points.
Based upon dosimetry studies with [111In]-radiolabelled Zevalin, the estimated radiation dosimetry for
individual organs following administration of [90Y]-radiolabelled Zevalin at activities of 15 MBq/kg
and 11 MBq/kg was calculated according to Medical Internal Radiation Dosimetry (MIRD) (Table 3).
The estimated radiation-absorbed doses to normal organs were substantially below recognised upper
safety limits. Individual patient dosimetry results were not predictive for [90Y]-radiolabelled Zevalin
toxicity.
Estimated Radiation Absorbed Doses From [90Y]-Zevalin
[90Y]-Zevalin mGy/MBq
Median Range
Lower Large Intestinal Wall1
Upper Large Intestinal Wall1
Heart Wall1
Small Intestine1
Red Marrow2
Urinary Bladder Wall3
Bone Surfaces2
Ovaries3
Adrenals3
Breasts3
Gallbladder Wall3
Pancreas3
Stomach3
Thyroid3
Kidneys1
Total Body3

12. INSTRUCTIONS FOR PREPARATION OF RADIOPHARMACEUTICALS
Read complete directions thoroughly before starting the preparation procedure. Proper aseptic technique and precautions for handling radioactive materials must be employed. Waterproof gloves must be utilised in the preparation and during the determination of radiochemical purity of [90Y]-radiolabelled Zevalin. Radiation protection precaution in accordance with local regulations must be taken, since administration of radiopharmaceuticals creates risks for other persons from external radiation or contamination from spills of urine, vomiting, etc. Characteristics of yttrium-90  The following minimum yttrium-90 characteristics are recommended: Radioactivity concentration at time of use Total extractable activity to deliver at time of use  1.48 GBq corresponding to 0.44 ml to 0.89 ml of yttrium-90 solution Radiochemical purity of the yttrium-90 chloride Radionuclidic purity strontium-90 content  0.74 MBq strontium-90 / 37 GBq yttrium-90 * Metals to be included need to be based on the specific manufacturing process. Control of these
metals can be achieved either through process validation or release test.
 Additional testing that might be required for suitability assessment:
Process-specific impurities:
Total organic carbon (e.g. organic chelators) Process residuals (e.g. ammonia, nitrate) Total other Beta impurities (non-strontium-90) * Needs to be included as release test or controlled through process validation if above limit of quantitation Directions for radio-labelling of Zevalin with yttrium-90:
Sterile, pyrogen-free yttrium-90 chloride of the above specified quality must be used for the preparation of [90Y]-radiolabelled Zevalin. Before radiolabelling, bring refrigerated Zevalin cold kit to room temperature 25°C. Clean the rubber stopper of all cold kit vials and the yttrium-90 chloride vial with a suitable alcohol swab and allow to air dry. Place cold kit reaction vial in a suitable dispensing shield (plastic enclosed in lead). Step 1: Transfer sodium acetate solution to the reaction vial Using a 1-ml sterile syringe, transfer sodium acetate solution to reaction vial. The volume of sodium acetate solution added is equivalent to 1.2 times the volume of yttrium-90 chloride to be transferred in step 2. Step 2: Transfer yttrium-90 chloride to the reaction vial Aseptically transfer 1500 MBq of yttrium-90 chloride with a 1 ml sterile syringe to the reaction vial containing the sodium acetate solution transferred in step 1. Mix completely by coating the entire inner surface of the reaction vial. Mix by inversion, rolling the container, avoid foaming or agitating the solution. Step 3: Transfer ibritumomab tiuxetan solution to the reaction vial Using a 2-3 ml sterile syringe, transfer 1.3 ml ibritumomab tiuxetan solution to the reaction vial. Mix completely by coating the entire inner surface of the reaction vial. Mix by inversion, rolling the container, avoid foaming or agitating the solution. Incubate the yttrium-90 chloride/acetate/ibritumomab tiuxetan solution at room temperature for five minutes. Labelling time longer than six minutes or shorter than four minutes will result in inadequate radioincorporation. Step 4: Add the formulation buffer to the reaction vial Using a 10-ml syringe with a large bore needle (18-20 G), draw formulation buffer that will result in a combined total volume of 10 ml. After the 5-minute incubation period, withdraw from the reaction vial the same volume of air as the formulation buffer to be added in order to normalise pressure and immediately thereafter gently add the formulation buffer down the side of the reaction vial to terminate incubation. Do not foam, shake, or agitate the mixture. Step 5: Assay the [90Y]-radiolabelled Zevalin solution for its specific radioactivity Radiochemical purity of the radiolabelled preparation applies as long as more than 95% of yttrium-90 is incorporated into the monoclonal antibody. Before administration to the patient, the percent radioincorporation of the prepared [90Y]-radiolabelled Zevalin must be checked according to the procedure outlined below. Caution: Patient dose not to exceed 1200 MBq. Instructions for determining the percent radioincorporation The radioincorporation assay for radiochemical purity, is performed by Instant Thin Layer Chromatography (ITLC) and must be carried out according to the following procedure. Required materials not supplied in the Zevalin kit: - Developing chamber for chromatography - Mobile phase: sodium chloride 9 mg/ml (0.9%) solution, bacteriostatic-free - ITLC strips (e.g. ITLC TEC-Control Chromatography Strips, Biodex, Shirley, New York, USA, Art. Nr. 150-772 or equivalent, dimensions: approximately 0.5-1 cm x 6 cm) - Scintillation vials - Liquid scintillation cocktail (e.g. Ultima Gold, catalog No. 6013329, Packard Instruments, USA or Assay procedure: 1.) Add approximately 0.8 ml sodium chloride 9 mg/ml (0.9%) solution to developing chamber assuring the liquid will not touch the 1.4 cm origin mark on the ITCL strip. 2.) Using a 1 ml insulin syringe with a 25- to 26-G needle, place a hanging drop (7-10 µl) of [90Y]-radiolabelled Zevalin onto the ITLC strip at its origin. Spot one strip at a time and run three ITLC strips. It may be necessary to perform a dilution (1:100) before application of the [90Y]-radiolabelled Zevalin to the ITLC strips. 3.) Place ITLC strip in the developing chamber and allow the solvent front to migrate past the 5.4 cm mark. 4.) Remove ITLC strip and cut in half at the 3.5 cm cut line. Place each half into separate scintillation vials to which 5 ml LSC cocktail must be added (e.g. Ultima Gold, catalog No. 6013329, Packard Instruments, USA or equivalent). Count each vial in a beta counter or in an appropriate counter for one minute (CPM), record net counts, corrected for background. 5.) Calculate the average Radiochemical Purity (RCP) as follows: 6.) Average % RCP = 7.) If the average radiochemical purity is less than 95%, the preparation must not be administered.

Source: http://www.radio-pharm.de/downloads/EU/emea-SmPC-h547en_May2013.pdf