Summary of medicine characteristics - ICATIBANT TEVA 30 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
Icatibant Teva 30 mg Solution for Injection in Pre-filled Syringe
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each pre-filled syringe of 3 ml contains icatibant acetate equivalent to 30 mg icatibant.
Each ml of the solution contains 10 mg of icatibant.
For the full list of excipients, see section 6.1.
3 PHARMACEUTICAL FORM
Solution for injection in pre-filled syringe (injection).
The solution is a clear and colourless liquid.
pH: 5.2–5.8
Osmolality: 285–330 mOsm/kg
4.1 Therapeutic indications
Icatibant Teva is indicated for symptomatic treatment of acute attacks of hereditary angioedema (HAE) in adults, adolescents and children aged 2 years and older, with C1-esterase-inhibitor deficiency.
4.2 Posology and method of administration
Icatibant Teva is intended for use under the guidance of a healthcare professional.
Posology
Adults
The recommended dose for adults is a single subcutaneous injection of Icatibant Teva 30 mg.
In the majority of cases a single injection of Icatibant Teva is sufficient to treat an attack. In case of insufficient relief or recurrence of symptoms, a second injection of Icatibant Teva can be administered after 6 hours. If the second injection produces insufficient relief or a recurrence of symptoms is observed, a third injection of Icatibant Teva can be administered after a further 6 hours. No more than 3 injections of Icatibant Teva should be administered in a 24 hour period.
In the clinical trials, not more than 8 injections of icatibant per month have been administered.
Paediatric population
The recommended dose of Icatibant Teva based on body weight in children and adolescents (aged 2 to 17 years) is provided in table 1 below.
Table 1: Dosage regimen for paediatric patients
| Body Weight | Dose (Injection Volume) |
| 12 kg to 25 kg | 10 mg (1.0 ml) |
| 26 kg to 40 kg | 15 mg (1.5 ml) |
| 41 kg to 50 kg | 20 mg (2.0 ml) |
| 51 kg to 65 kg | 25 mg (2.5 ml) |
| >65 kg | 30 mg (3.0 ml) |
In the clinical trial, not more than 1 injection of icatibant per HAE attack has been administered.
No dosage regimen for children aged less than 2 years or weighing less than 12 kg can be recommended as the safety and efficacy in this paediatric group has not been established.
Elderly
Limited information is available on patients older than 65 years of age.
Elderly people have been shown to have increased systemic exposure to icatibant. The relevance of this to the safety of Icatibant Teva is unknown (see section 5.2).
Hepatic impairment
No dose adjustment is required in patients with hepatic impairment.
Renal impairment
No dose adjustment is required in patients with renal impairment.
Method of administration
Icatibant Teva is intended for subcutaneous administration preferably in the abdominal area.
Icatibant Teva solution for injection should be injected slowly due to the volume to be administered.
Each Icatibant Teva syringe is intended for single use only.
Refer to the patient information leaflet for instructions for use.
Caregiver/self-administration
The decision on initiating caregiver or self-administration of Icatibant Teva should only be taken by a physician experienced in the diagnosis and treatment of hereditary angioedema (see section 4.4).
Adults
Icatibant Teva may be self-administered or administered by a caregiver only after training in subcutaneous injection technique by a healthcare professional.
Children and adolescents aged 2–17 years
Icatibant Teva may be administered by a caregiver only after training in subcutaneous injection technique by a healthcare professional.
4.3 Contraindications
Hypersensitivity to the active substance or to any of the excipients listed in section 6.1.
4.4 Special warnings and precautions for use
Laryngeal attacks
Patients with laryngeal attacks should be managed in an appropriate medical institution after injection until the physician considers discharge to be safe.
Ischemic heart disease
Under ischemic conditions, a deterioration of cardiac function and a decrease in coronary blood flow could theoretically arise from antagonism of bradykinin receptor type 2. Caution should therefore be observed in the administration of Icatibant Teva to patients with acute ischemic heart disease or unstable angina pectoris (see section 5.3).
Stroke
Although there is evidence to support a beneficial effect of B2 receptor blockade immediately following a stroke, there is a theoretical possibility that icatibant may attenuate the positive late phase neuroprotective effects of bradykinin. Accordingly, caution should be observed in the administration of icatibant to patients in the weeks following a stroke.
Caregiver/self-administration
For patients who have never received Icatibant Teva previously, the first treatment should be given in a medical institution or under the guidance of a physician.
In case of insufficient relief or recurrence of symptoms after self-treatment or administration by a caregiver, it is recommended that the patient or caregiver should seek medical advice. For adults, subsequent doses that may be required for the same attack should be administered within a medical institution (see section 4.2). There are no data on administering subsequent doses for the same attack in adolescents or children.
Patients experiencing a laryngeal attack should always seek medical advice and be observed in a medical institution also after having taken the injection at home.
Paediatric population
There is limited experience with treatment of more than one HAE attack with icatibant in the paediatric population.
Sodium content
This medicine contains less than 1 mmol sodium (23 mg) per 3 ml, that is to say essentially ‘sodium-free’.
4.5 Interaction with other medicinal products and other forms of interaction
Pharmacokinetic drug interactions involving CYP450 are not expected (see section 5.2).
Co-administration of icatibant with angiotensin-converting-enzyme (ACE) inhibitors has not been studied. ACE inhibitors are contraindicated in HAE patients due to possible enhancement of bradykinin levels.
Paediatric population
Interaction studies have only been performed in adults.
4.6 Fertility, pregnancy and lactation
Pregnancy
For icatibant, no clinical data on exposed pregnancies are available. Animal studies showed effects on uterine implantation and parturition (see section 5.3), but the potential risk for humans is unknown.
Icatibant Teva should be used during pregnancy only, if the potential benefit justifies the potential risk for the foetus, (e.g. for treatment of potentially life threatening laryngeal attacks).
Breast-feeding
Icatibant is excreted in the milk of lactating rats at concentrations similar to those in maternal blood. No effects were detected in the post-natal development of rat pups.
It is unknown whether icatibant is excreted in human breast milk but it is recommended that breastfeeding women, who wish to take Icatibant Teva, should not breastfeed for 12 hours after treatment.
Fertility
In both rats and dogs, repeated use of icatibant resulted in effects on reproductive organs. Icatibant had no effect on the fertility of male mice and rats (see section 5.3).
In a study of 39 healthy adult men and women treated with 30 mg every 6 hours for 3 doses every 3 days for a total of 9 doses, there were no clinically significant changes from baseline in basal and GnRH-stimulated concentration of reproductive hormones in either females or males. There were no significant effects of icatibant on the concentration of luteal phase progesterone and luteal function, or on menstrual cycle length in females and there were no significant effects of icatibant on sperm count, motility and morphology in males. The dosing regimen used for this study is unlikely to be sustained in the clinical setting.
4.7 Effects on ability to drive and use machines
Icatibant Teva has minor influence on the ability to drive and use machines. Fatigue, lethargy, tiredness, somnolence, and dizziness have been reported following the use of icatibant. These symptoms may occur as a result of an attack of HAE. Patients should be advised not to drive and use machines if they feel tired or dizzy.
4.8 Undesirable effects
Summary of the safety profile
In clinical studies used for registration, a total of 999 HAE attacks have been treated with 30 mg icatibant administered subcutaneously by a healthcare professional.
Icatibant 30 mg SC has been administered by a healthcare professional to 129 healthy subjects and 236 patients with HAE.
Almost all subjects who were treated with subcutaneous icatibant in clinical trials developed reactions at the site of injection (characterised by skin irritation, swelling, pain, itchiness, erythema, burning sensation). These reactions were generally mild to moderate in severity, transient, and resolved without further intervention.
Tabulated list of adverse reactions
The frequency of adverse reactions listed in Table 1 is defined using 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); unknown (frequency cannot be estimated from the available data).
All adverse reactions from post-marketing experience are italicised.
Table 2: Adverse reactions reported with icatibant
| System Organ Class (incidence category) | Preferred Term |
| Nervous system disorders (Common, >1/100 to <1/10) | Dizziness Headache |
| Gastrointestinal disorders (Common, >1/100 to <1/10) | Nausea |
| Skin and subcutaneous tissue disorders (Common, >1/100 to <1/10) (Unknown) | Rash Erythema Pruritus Urticaria |
| General disorders and administration site conditions (Very Common, >1/10) (Common, >1/100 to <1/10) | Injection site reactions* Pyrexia |
| Investigations (Common, >1/100 to <1/10) | Transaminases increased |
| * Injection site bruising, Injection site hematoma, Injection site burning, Injection site erythema, Injection site hypoesthesia, Injection site irritation, Injection site numbness, Injection site edema, Injection site pain, Injection site pressure sensation, Injection site pruritus, Injection site swelling, Injection site urticaria, and Injection site warmth | |
Paediatric Population
A total of 32 paediatric patients (8 children aged 2 to 11 years and 24 adolescents aged 12 to 17 years) with HAE were exposed to treatment with icatibant during clinical studies. Thirty-one patients received a single dose of icatibant and 1 patient (an adolescent) received icatibant for two HAE attacks (in total, two doses). Icatibant was administered by subcutaneous injection at a dose of 0.4 mg/kg based on body weight to a maximum dose of 30 mg.
The majority of paediatric patients who were treated with subcutaneous icatibant experienced injection site reactions such as erythema, swelling, burning sensation, skin pain and itching/pruritus; these were found to be mild to moderate in severity and consistent with reactions that have been reported in adults. Two paediatric patients experienced injection site reactions which were assessed as severe and which were completely resolved within 6 hours. These reactions were erythema, swelling, burning and warm sensation.
No clinically significant changes in reproductive hormones were observed during clinical studies.
Description of selected adverse reactions
Immunogenicity
Across repeated treatment in adults in the controlled phase III trials, transient positivity to anti-icatibant antibodies was observed in rare cases. All patients maintained efficacy. One icatibant-treated patient tested positive for anti-icatibant antibodies before and after treatment with icatibant. This patient was followed for 5 months and further samples were negative for anti-icatibant antibodies. No hypersensitivity or anaphylactic reactions were reported with icatibant.
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after 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 via the Yellow Card Scheme
Website: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.
4.9 Overdose
4.9 OverdoseNo clinical information on overdose is available.
A dose of 3.2 mg/kg intravenously (approximately 8 times the therapeutic dose) caused transient erythema, itching, flushing or hypotension in healthy subjects. No therapeutic intervention was necessary.
5 PHARMACOLOGICAL PROPERTIES
5.1 Pharmacodynamic properties
Pharmacotherapeutic group: Other haematological agents, drugs used to treat hereditary angioedema; ATC code: B06AC02.
Mechanism of action
HAE (an autosomal dominant disease) is caused by an absence or dysfunction of C1-esterase-inhibitor. HAE attacks are accompanied by an increased release of bradykinin, which is the key mediator in the development of the clinical symptoms.
HAE manifests as intermittent attacks of subcutaneous and/or sub mucosal oedema involving the upper respiratory tract, the skin and the gastrointestinal tract. An attack usually lasts between 2 to 5 days.
Icatibant is a selective competitive antagonist at the bradykinin type 2 (B2) receptor. It is a synthetic decapeptide with a structure similar to bradykinin, but with 5 non-proteinogenic amino acids. In HAE increased bradykinin concentrations are the key mediator in the development of the clinical symptoms.
Pharmacodynamic effects
In healthy young subjects, icatibant administered in doses of 0.8 mg/kg over 4 hours; 1.5 mg/kg/day or 0.15 mg/kg/day for 3 days, development of bradykinin-induced hypotension, vasodilatation and reflex tachycardia was prevented. Icatibant was shown to be a competitive antagonist when the bradykinin challenge dose was increased 4-fold.
Clinical efficacy and safety
Efficacy data were obtained from an initial open-label Phase II study and from three controlled Phase III studies.
Phase III clinical studies (FAST-1 and FAST-2) were randomized, double-blind, controlled trials and had identical designs except for the comparator (one with oral tranexamic acid as the comparator and one placebo controlled). A total of 130 patients were randomized to receive either a 30 mg dose of icatibant (63 patients) or comparator (either tranexamic acid, – 38 or placebo – 29 patients).
Subsequent episodes of HAE were treated in an open label extension. Patients with symptoms of laryngeal angioedema received open label treatment with icatibant. The primary efficacy endpoint was the time to onset of symptom relief using a visual analogue scale (VAS). Table 3 shows the efficacy results for these studies.
FAST-3 was a randomized, placebo-controlled, parallel-group study of 98 adult patients with a median age of 36 years. Patients were randomized to receive either icatibant 30 mg or placebo by subcutaneous injection. A subset of patients in this study experienced acute HAE attacks while receiving androgens, antifibrinolytic agents or Cl inhibitors. The primary endpoint was time to onset of symptom relief assessed using a 3-item composite visual analog score (VAS-3) consisting of assessments of skin swelling, skin pain, and abdominal pain. Table 4 shows the efficacy results for FAST-3.
In these studies, patients on icatibant had a faster median time to onset of symptom relief (2.0, 2.5 and 2.0 hours, respectively) compared to tranexamic acid (12.0 hours) and placebo (4.6 and 19.8 hours). The treatment effect of icatibant was confirmed by secondary efficacy endpoints.
In an integrated analysis of these controlled Phase III studies, the time to onset of symptom relief and time to onset of primary symptom relief were similar regardless of age group, sex, race, weight or whether or not the patient used androgens or antifibrinolytic agents.
Response was also consistent across repeated attacks in the controlled Phase III trials. A total of 237 patients were treated with 1,386 doses of 30 mg icatibant for 1,278 attacks of acute HAE. In the first 15 icatibant treated attacks (1,114 doses for 1,030 attacks), the median times to onset of symptom relief were similar across attacks (2.0 to 2.5 hours). 92.4% of these attacks of HAE were treated with a single dose of icatibant.
Table 3. Efficacy results for FAST-1 and FAST-2
| Controlled Clinical Study of ICATIBANT vs Tranexamic acid or Placebo: Efficacy Results | |||||
| FAST-2 | FAST-1 | ||||
| Icatibant | Tranexamic acid | Icatibant | Placebo | ||
| Number of subjects in ITT Population | 36 | 38 | Number of subjects in ITT Population | 27 | 29 |
| Baseline VAS(mm) | 63.7 | 61.5 | Baseline VAS(mm) | 69.3 | 67.7 |
| Change from baseline to 4 hours | –41.6 | –14.6 | Change from baseline to 4 hours | –44.8 | –23.5 |
| Difference between treatments (95% CI, p-value) | –27.8 (-39.4, –16.2) p < 0.001 | Difference between treatments (95% CI, p-value) | –23.3 (-37.1, –9.4) p = 0.002 | ||
| Change from baseline to 12 hours | –54.0 | –30.3 | Change from baseline to 12 hours | –54.2 | –42.4 |
| Difference between treatments (95% CI, p-value) | –24.1 (-33.6, –14.6) p < 0.001 | Difference between treatments (95% CI, p-value) | –15.2 (-28.6, –1.7) p = 0.028 | ||
| Median time to onset of symptom relief (hours) | Median time to onset of symptom relief (hours) | ||||
| All episodes (N = 74) | 2.0 | 12.0 | All episodes (N = 56) | 2.5 | 4.6 |
| Response rate (%, CI) at 4 hours after start of treatment | Response rate (%, CI) at 4 hours after start of treatment | ||||
| Controlled Clinical Study of ICATIBANT vs Tranexamic acid or Placebo: Efficacy Results | |||||
| FAST-2 | FAST-1 | ||||
| Icatibant | Tranexamic acid | Icatibant | Placebo | ||
| All episodes (N = 74) | 80.8 (63.1, 91.6) | 30.6 (16.3, 48.1) | All episodes (N = 56) | 66.7 (46.0, 83.5) | 46.4 (27.5, 66.1) |
| Median time to onset of symptom relief: all symptoms (hours): Abdominal pain Skin swelling Skin pain | 1.6 2.6 1.5 | 3.5 18.1 12.0 | Median time to onset of symptom relief: all symptoms (hours): Abdominal pain Skin swelling Skin pain | 2.0 3.1 1.6 | 3.3 10.2 9.0 |
| Median time to almost complete symptom relief (hours) | Median time to almost complete symptom relief (hours) | ||||
| All episodes (N = 74) | 10.0 | 51.0 | All episodes (N = 56) | 8.5 | 19.4 |
| Median time to regression of symptoms, by patient (hours) | Median time to regression of symptoms, by patient (hours) | ||||
| All episodes (N = 74) | 0.8 | 7.9 | All episodes (N = 56) | 0.8 | 16.9 |
| Median time to overall patient improvement, by physician (hours) | Median time to overall patient improveme nt, by physician | ||||
| Controlled Clinical Study of ICATIBANT vs Tranexamic acid or Placebo: Efficacy Results | |||||
| FAST-2 | FAST-1 | ||||
| Icatibant | Tranexamic acid | Icatibant | Placebo | ||
| (hours) | |||||
| All episodes (N = 74) | 1.5 | 6.9 | All episodes (N = 56) | 1.0 | 5.7 |
Table 4. Efficacy results for FAST-3
| Efficacy Results: FAST-3; Controlled Phase – ITT population | ||||
| Endpoint | Statistic | Icatibant | Placebo | p-value |
| (n = 43) | (n = 45) | |||
| Primary Endpoint | ||||
| Time to Onset of Symptom Relief-Composite VAS (hrs) | Median | 2.0 | 19.8 | <0.001 |
| Other Endpoints | ||||
| Time to Onset of Primary Symptom Relief (hrs) | Median | 1.5 | 18.5 | <0.001 |
| Change in Composite VAS Score at 2 hrs after treatment | Mean | –19.74 | –7.49 | <0.001 |
| Change in Composite Subject-Assessed Symptom Score at 2 hours | Mean | –0.53 | –0.22 | <0.001 |
| Change in Composite Investigator-Assessed Symptom Score at 2 hours | Mean | –0.44 | –0.19 | <0.001 |
| Time to Almost Complete Symptom Relief (hrs) | Median | 8.0 | 36.0 | 0.012 |
| Time to Subject-Assessed Initial Symptom Improvement (hrs) | Median | 0.8 | 3.5 | <0.001 |
| Time to Investigator-Assessed Initial Visual Symptom Improvement (hrs) | Median | 0.8 | 3.4 | <0.001 |
A total of 66 patients with attacks of HAE affecting the larynx were treated in these controlled Phase III clinical trials. The results were similar to patients with non-laryngeal attacks of HAE with respect to time to onset of symptom relief.
Paediatric population
An open label, non-randomised single-arm study (HGT-FIR-086) was performed with a total of 32 patients. All patients received at least one dose of icatibant (0.4 mg/kg body weight up to a maximum dose of 30 mg) and the majority of patients were followed up for a minimum of 6 months. Eleven patients were of prepubertal status and 21 patients were either pubertal or postpubertal.
The efficacy population consisted of 22 patients who had been treated with icatibant (11 prepubertal and 11 pubertal/postpubertal) for HAE attack.
The primary efficacy endpoint was the time to onset of symptom relief (TOSR) measured using a composite investigator-reported symptom score. Time to symptom relief was defined as the duration of time (in hours) taken for improvement of symptoms to occur by a magnitude of 20%.
Overall the median time to onset of symptom relief was 1.0 hour (95% confidence interval, 1.0–1.1 hours). At 1 and 2 hours post treatment, approximately 50% and 90% of patients experienced onset of symptom relief, respectively.
Overall, the median time to minimal symptoms (earliest time post treatment when all symptoms were either mild or absent) was 1.1 hours (95% confidence interval, 1.02.0 hours).
5.2 Pharmacokinetic properties
The pharmacokinetics of icatibant has been characterized by studies using both intravenous and subcutaneous administration to healthy volunteers and patients. The pharmacokinetic profile of icatibant in patients with HAE is similar to that in healthy volunteers.
Absorption
Following subcutaneous administration, the absolute bioavailability of icatibant is 97%. The time to maximum concentration is approximately 30 minutes.
Distribution
Icatibant volume of distribution (Vss) is about 20–25 L. Plasma protein binding is 44%.
Biotransformation
Icatibant is extensively metabolized by proteolytic enzymes to inactive metabolites that are primarily excreted in the urine.
In vitro studies have confirmed that icatibant is not degraded by oxidative metabolic pathways and is not an inhibitor of major cytochrome P450 (CYP) isoenzymes (CYP 1A2, 2A6, 2B6, 2C8, 2C9, 2C19, 2D6, 2E1, and 3A4) and is not an inducer of CYP 1A2 and 3A4.
Elimination
Icatibant is mainly eliminated by metabolism with less than 10% of the dose eliminated in the urine as unchanged drug. Clearance is about 15–20 l/h and independent of dose. The terminal plasma half-life is about 1–2 hours.
Special populations
Elderly
Data suggest an age-related decline in clearance resulting in about 50–60% higher exposure in older people (75–80 years) compared to patients aged 40 years.
Gender
Data suggest that there is no difference in the clearance between females and males after correcting for body weight.
Hepatic and Renal Impairment
Limited data suggest that icatibant exposure is not influenced by hepatic or renal impairment.
Race
Information on individual race effect is limited. Available exposure data suggest no difference in the clearance between non-White (n=40) and White (n=132) subjects.
Paediatric population
The pharmacokinetics of icatibant were characterized in paediatric HAE patients in study HGT-FIR-086 (see section 5.1). Following a single subcutaneous administration (0.4 mg/kg up to a maximum of 30 mg), the time to maximum concentration is approximately 30 minutes and the terminal half-life is about 2 hours. There are no observed differences in the exposure to icatibant between HAE patients with and without an attack. Population pharmacokinetic modelling using both adult and paediatric data showed that clearance of icatibant is related to body weight with lower clearance values noted for lower body weights in the paediatric HAE population. Based on modelling for weight banded dosing, the predicted exposure to icatibant in the paediatric HAE population (see section 4.2) is lower than the observed exposure in studies conducted with adult HAE patients.
5.3 Preclinical safety data
6 PHARMACEUTICAL PARTICULARS
6.1 List of excipients
Sodium chloride
Acetic acid, glacial (for pH adjustment) Sodium hydroxide (for pH adjustment) Water for injections
6.2 Incompatibilities
Not applicable.
6.3 Shelf life
2 years
6.4 Special precautions for storage
Do not store above 25°C.
Do not freeze.
6.5 Nature and contents of container
3 ml of solution in a 3 ml pre-filled syringe (type I glass) with plunger stopper (bromobutyl coated with fluorocarbon polymer). A hypodermic needle (25 G; 16 mm) is included in the pack.
Pack size of one pre-filled syringe with one needle or a multipack containing three pre-filled syringes with three needles (3 single packs).
Not all pack sizes may be marketed.
6.6 Special precautions for disposal
6.6 Special precautions for disposalThe solution should be clear and colourless and free from visible particles.
Paediatric use
The appropriate dose to be administered is based on body weight (see section 4.2).
Where the required dose is less than 30 mg (3 ml), the following equipment is required to extract and administer the appropriate dose:
Adapter (proximal and/or distal female luer lock connector/coupler)
3 ml (recommended) graduated syringe
The pre-filled icatibant syringe and all other components are for single use only.
Any unused product or waste material should be disposed of in accordance with local requirements.
All needles and syringes should be disposed of in a sharps container.