Replenine-Vf 50 Iu/Ml Human Factor Ix A Powder For Solution
Out of date information, search anotherSUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
REPLENINE ®-VF, 50 IU/ml human factor IX, a powder for solution.
2. QUALITATIVE AND QUANTITATIVE COMPOSITION
Replenine-VF is a high purity factor IX. This product is prepared from plasma from screened donors. Donors are selected from the USA.
Replenine-VF is presented as a sterile powder for solution, containing nominally 250 IU, 500 IU or 1000 IU human coagulation factor IX per vial. The product contains approximately 50 IU/mL when reconstituted with either 5 mL (250 IU vial), 10 mL (500 IU vial) or 20 mL (1000 IU Vial) of Sterilised Water for Injections, (Ph.Eur.).
One mL of Replenine-VF contains approximately 100 IU of human coagulation factor IX after reconstitution at half volume (see 6.6).
The potency (IU) is determined using the European Pharmacopoeia one stage clotting test. The specific activity of Replenine-VF is approximately 100 IU per mg of protein.
For excipients, see section 6.1.
3 PHARMACEUTICAL FORM
REPLENINE®-VF is a powder for solution, it is a freeze-dried concentrate of factor IX for reconstitution with Sterilised Water for Injections, Ph.Eur. After reconstitution with the supplied sterile water diluent the product is administered intravenously.
4 CLINICAL PARTICULARS
4.1 Therapeutic indications
Treatment and prophylaxis of bleeding in patients with haemophilia B (congenital factor IX deficiency).
4.2 Posology and method of administration
Treatment should be initiated under the supervision of a physician experienced in the treatment of haemophilia.
Posology
The dosage and duration of the substitution therapy depend on the severity of the factor IX deficiency, on the location and extent of the bleeding and on the patient’s clinical condition.
On demand treatment
The number of units of factor IX administered is expressed in International Units (IU), which are related to the current WHO standard for factor IX products. Factor IX activity in plasma is expressed either as a percentage (relative to normal human plasma) or in International Units (relative to an international standard for factor IX in plasma).
One International Unit (IU) of factor IX activity is equivalent to that quantity of factor IX in one mL of normal human plasma. The calculation of the required dosage of factor IX is based on the empirical finding that 1 International Unit (IU) Replenine-VF per kg body weight raises the plasma factor IX activity by 1.16% of normal activity. The required dosage is determined using the following formula:
Required units = body weight (kg) x desired factor IX rise (%) (IU/dL) x 0.85
The amount to be administered and the frequency of administration should always be orientated to the clinical effectiveness in the individual case. Factor IX products rarely require to be administered more than once daily.
In the case of the following haemorrhagic events, the factor IX activity should not fall below the given plasma activity level (in IU/dL) in the corresponding period. The following table can be used to guide dosing in bleeding episodes and surgery:
|
Degree of haemorrhage/ Type of surgical procedure |
Factor IX level required (%) (IU/dL) |
Frequency of doses (hours)/ Duration of Therapy (days) |
|
Haemorrhage | ||
|
Early haemarthrosis, muscle bleed or oral bleeding |
20-40 |
Repeat every 24 hours. At least 1 day, until the bleeding episode as indicated by pain is resolved or healing is achieved. |
|
More extensive haemarthrosis, muscle bleeding or haematoma. |
30-60 |
Repeat infusion every 24 hours for 3 to 4 days or more until pain and disability are resolved. |
|
Life threatening haemorrhages. |
60-100 |
Repeat infusion every 8 to 24 hours until threat is resolved. |
|
Surgery | ||
|
Minor surgery Including tooth extraction |
30-60 |
Every 24 hours, at least 1 day, until healing is achieved. |
|
Major surgery |
80-100 (pre- and postoperative) |
Repeat infusion every 8 to 24 hours until adequate wound healing, then therapy for at least another 7 days to maintain a F IX activity of 30% to 60% (IU/dL). |
Prophylaxis
For long term prophylaxis against bleeding in patients with severe haemophilia B, the usual doses are 20 to 40 IU of factor IX per kilogram of body weight at intervals of 3 to 4 days.
In some cases, especially in younger patients, shorter dosage intervals or higher doses may be necessary.
Continuous infusion
Prior to surgery, a pharmacokinetic analysis should be performed to obtain an estimate of clearance. The initial infusion rate can be calculated as follows:
Clearance x Desired steady state level = Infusion rate (IU/kg/h)
After the initial 24 hours of continuous infusion, the clearance should be calculated again every day using the steady state equation with the measured level and the known rate of infusion (see also section 5.2).
During the course of treatment, appropriate determination of factor IX levels is advised to guide the dose to be administered and the frequency of repeated infusions. In the case of major surgical interventions in particular, precise monitoring of the substitution therapy by means of coagulation analysis (plasma factor IX activity) is indispensable. Individual patients may vary in their response to factor IX, achieving different levels of in vivo recovery and demonstrating different half-lives.
In a clinical study in children under six years of age, the median dose of Replenine-VF for prophylaxis was 29.3 IU/kg (95% confidence interval: 25.3 - 33.2 IU/kg) given up to twice weekly; the mean dose to treat a bleed was 26.8 IU/kg (95% confidence interval 15.7 - 37.9 IU/kg).
Patients should be monitored for the development of factor IX inhibitors. If the expected factor IX activity plasma levels are not attained, or if bleeding is not controlled with an appropriate dose, an assay should be performed to determine if a factor IX inhibitor is present. In patients with high levels of inhibitor, factor IX therapy may not be effective and other therapeutic options should be considered. Management of such patients should be directed by physicians with experience in the care of patients with haemophilia.
See also 4.4.
Method of administration
Reconstitute the product as described in 6.6. The product should be administered via the intravenous route. The dose, especially the first dose, should be given slowly (not more than 3 mL per minute).
For continuous infusion during and after major surgery, the product should be given intravenously and undiluted by a syringe driver or syringe pump (see 4.2).
4.3 Contraindications
Hypersensitivity to the active substance or to any of the excipients.
4.4 Special warnings and special precautions for use
As with any intravenous protein product, allergic type hypersensitivity reactions are possible. Replenine-VF contains traces of human proteins other than FIX. Patients should be informed of the early signs of hypersensitivity reactions including hives, generalised urticaria, tightness of the chest, wheezing, hypotension and anaphylaxis. If these symptoms occur, they should be advised to discontinue use of the product immediately and contact their physician. In case of shock, standard treatment for shock-treatment should be observed.
Standard measures to prevent infections resulting from the use of medicinal products prepared from human blood or plasma include selection of donors, screening of individual donations and plasma pools for specific markers of infection and the inclusion of effective manufacturing steps for the inactivation/removal of viruses. Despite this, when medicinal products prepared from human blood or plasma are administered, the possibility of transmitting infective agents cannot be totally excluded. This also applies to unknown or emerging viruses and other pathogens.
The measures taken are considered effective for enveloped viruses such as HIV, HBV and HCV, and for the non-enveloped viruses HAV and parvovirus B19.
It is strongly recommended that every time that Replenine-VF is administered to a patient, the name and batch number of the product are recorded in order to maintain a link between the patient and the batch of the product.
After repeated treatment with human coagulation factor IX products, patients should be monitored for the development of neutralising antibodies (inhibitors) that should be quantified in Bethesda Units (BU) using appropriate biological testing.
There have been reports in the literature showing a correlation between the occurrence of a factor IX inhibitor and allergic reactions. Therefore, patients experiencing allergic reactions should be evaluated for the presence of an inhibitor. It should be noted that patients with factor IX inhibitors may be at an increased risk of anaphylaxis with subsequent challenge with factor IX. Because of the risk of allergic reactions with factor IX concentrates, the initial administrations of factor IX should, according to the treating physician’s judgement, be performed under medical observation where proper medical care for allergic reactions could be provided.
Since the use of factor IX complex concentrates has historically been associated with the development of thromboembolic complications, the risk being higher in low purity preparations, the use of factor IX containing products may be potentially hazardous in patients with signs of fibrinolysis and in patients with disseminated intravascular coagulation (DIC). Because of the potential risk of thrombotic complications, clinical surveillance for early signs of thrombotic and consumptive coagulopathy should be initiated with appropriate biological testing when administering this product to patients with liver disease, to patients post-operatively, to new-born infants, or to patients at risk of thromboembolic phenomena or DIC. In each of these situations, the potential benefit of treatment with Replenine-VF should be weighed against the risk of these complications.
4.5 Interaction with other medicinal products and other forms of interaction
No interactions of human coagulation factor IX products with other medicinal products are known.
4.6 Pregnancy and lactation
Animal reproduction studies have not been conducted with factor IX. Based on the rare occurrence of haemophilia B in women, experience regarding the use of factor IX during pregnancy and breast-feeding is not available. Therefore, REPLENINE®-VF should be used during pregnancy and lactation only if clearly indicated.
4.7 Effects on ability to drive and use machines
Replenine-VF has no influence on the ability to drive and use machines.
4.8 Undesirable effects
The following adverse reactions have been reported from patients in clinical studies and from post-marketing experience (common > 1/100 to <1/10).
|
MedDRA Standard System Organ Class |
Adverse reactions |
Frequency |
|
Nervous system disorders |
Headache |
common |
|
General disorders and injection site changes |
injection site reaction |
common |
Hypersensitivity or allergic reactions (which may include angioedema, burning and stinging at the infusion site, chills, flushing, generalised urticaria, headache, hives, hypotension, lethargy, nausea, restlessness, tachycardia, tightness of the chest, tingling, vomiting, wheezing) have been observed infrequently in patients treated with factor IX containing products. In some cases, these reactions have progressed to severe anaphylaxis, and they have occurred in close temporal association with development of factor IX inhibitors (see also 4.4).
Nephrotic syndrome has been reported following attempted immune tolerance induction in haemophilia B patients with factor IX inhibitors and a history of allergic reaction.
On rare occasions, fever has been observed.
Patients with haemophilia B may develop antibodies (inhibitors) to factor IX. If such inhibitors occur, the condition will manifest as an insufficient clinical response. In such cases, it is recommended that a specialised haemophilia centre be contacted. In a clinical study in children aged less than six years, three previously untreated patients were enrolled and remained inhibitor negative after treatment with Replenine-VF for six months. Of the 67 previously tested patients in clinical studies, one young child developed an inhibitor with a titre of 3.6 Bethesda Units.
There is a potential risk of thromboembolic episodes following the administration of factor IX products, with a higher risk for low purity preparations. The use of low purity factor IX products has been associated with instances of myocardial infarction, disseminated intravascular coagulation, venous thrombosis and pulmonary embolism. The use of high purity factor IX is rarely associated with such side effects.
For information on viral safety see 4.4
4.9 Overdose
No-case of overdose with human factor IX has been reported.
5.1 Pharmacodynamic properties
Pharmacotherapeutic group: Antihaemorrhagics: blood coagulation factor IX. ATC code: B02B D04
Factor IX is a single chain glycoprotein with a molecular mass of about 68,000 Daltons. It is a vitamin K-dependent coagulation factor and it is synthesised in the liver.
Factor IX is activated by factor XIa in the intrinsic coagulation pathway and by the factor VII/tissue factor complex in the extrinsic pathway. Activated factor IX, in combination with activated factor VIII, activates factor X. Activated factor X converts prothrombin into thrombin. Thrombin then converts fibrinogen into fibrin and a clot is formed.
Haemophilia B is a sex-linked hereditary disorder of blood coagulation due to decreased levels of factor IX and results in profuse bleeding into joints, muscles or internal organs, either spontaneously or as a result of accidental or surgical trauma. By replacement therapy the plasma level of factor IX is increased, thereby enabling a temporary correction of the factor deficiency and correction of the bleeding tendencies.
From clinical trial experience, young children using prophylactic Replenine-VF experienced less bleeds than those only using it on demand. For doses in children see 4.2.
5.2 Pharmacokinetic properties
In a clinical study of 15 adult patients with haemophilia B, the mean pharmacokinetic properties of Replenine-VF were as follows:
Incremental Recovery: AUC0-56 h:
Terminal Half-life: Alpha Half-life: Beta-Half-life:
Mean Residence Time: Clearance:
Volume of Distribution: 1.16 IU/dL per IU/kg
15.2 IU.mL/hour 19.0 hours 4.8 hours
20.9 hours
24.9 hours
4.52 mL/hour/kg 122.1 mL/kg
From clinical studies in 48 adult patients with haemophilia B, most of whom had several assessments of incremental recovery, all based on the maximum FIX:C in the first 1 hour (ISTH, 2001), the overall results were as follows:
In a clinical trial, of Replenine-VF-given by continuous infusion to cover for major surgery, an initial bolus dose was given to raise the factor IX activity to about 100 IU/dL. Continuous infusion was then started at 6 IU/kg/hour (given undiluted by syringe pump or syringe driver). Subsequently, the rate of infusion was adjusted according to the following formula:
New rate = Latest rate x_Target FIX level (IU/mL)
(IU/kg/hour) (IU/kg/hour) Recently recorded FIX
level (IU/mL)
The median clearance was fastest during the first 24 hours peri-operatively (Day 1). Thereafter, median clearance declined as follows: Day 1, 7.3 mL/kg/h; Day 2, 4.2 mL/kg/h; Day 3, 4.4 mL/kg/h; Day 4, 3.4 mL/kg/h; Day 5, 3.2 mL/kg/h; Day 6, 1.3 mL/kg/h. The formula describing the reduction in clearance from post-operative Days 2 to 8 was as follows:
Factor IX clearance (mL/h/kg) = 5.05 - (0.36 x day)
There was inter-patient variability in clearance so, when covering surgery by continuous infusion, monitoring of plasma factor IX activity is required (see section 4.2).
Additional data from the study of continuous infusion in major surgery provided the following mean pharmacokinetic values for the period on continuous infusion (by one-compartment multidose analysis):
|
Half-life: |
14.8 |
hours |
|
Mean Residence Time: |
31.3 |
hours |
|
Clearance: |
3.8 |
mL/hour/kg |
|
Volume of Distribution: |
107.0 |
mL/kg |
5.3 Preclinical safety data
Human plasma coagulation factor IX (as contained in REPLENINE®-VF) is a normal constituent of the human plasma and acts like the endogenous factor IX.
Repeated dose toxicity testing in animals is impracticable due to interference with developing antibodies to heterologous protein. Since clinical experience provides no evidence for tumourigenic and mutagenic effects of human plasma coagulation factor IX, experimental studies, particularly in heterologous species, are not considered necessary.
Single dose toxicity studies in rats and mice have established greater than a 20 fold safety margin. Thrombogenicity testing in rabbits and rats showed no evidence of thrombogenicity at doses of 200-300 IU/kg body weight.
6.1 List of excipients
REPLENINE®-VF solution contains the following excipients :
glycine
lysine
sodium citrate sodium phosphate sodium chloride polysorbate 80 tri-n-butyl phosphate.
6.2 Incompatibilities
This medicinal product must not be mixed with other medicinal products.
Only approved injection/infusion sets should be used with the reconstituted product because treatment failure may occur as a consequence of human factor IX adsorption to the internal surface of some unapproved infusion equipment.
6.3 Shelf life
When unopened, shelf-life is 36 months at 2°C to 8°C, up to 3 months at normal ambient temperature (25°C) within this period is not detrimental to the product. The expiry date is printed on the label.
When opened, store at 2°C to 25°C and use within one hour. Warm to ambient temperature (25°C) before injection.
Sterilised Water for Injections, Ph.Eur., should be stored between 2°C and 25°C.
The Transfer Device (Mix2VialTM) can be stored in the original carton with Replenine-VF at 2°C to 8°C.
6.4 Special precautions for storage
Store Replenine-VF in its carton to protect from light at the temperature specified on the packaging. DO NOT FREEZE. Do not use beyond the expiry date on the label. When the product is for home use a domestic refrigerator is suitable for storage.
6.5 Nature and contents of container
Replenine-VF is a freeze-dried plug of high purity factor IX supplied in a single dose vial of either 250 IU, 500 IU or 1000 IU (nominal). The product is contained in glass (type I Ph.Eur.), bottles stoppered with a halobutyl stopper. The bung is over-sealed with a snap-off polypropylene cap and a clear lacquered aluminium skirt.
Supplied with the product is a Transfer Device called Mix2VialTM to allow needle free, easy and safe reconstitution of the product with the Sterilised Water for Injections, Ph.Eur.
6.6 Instructions for use and handling and disposal
Reconstitute the product with the Sterilised Water for Injections, Ph.Eur., supplied (2.5 mL or 5 mL for 250 IU, 5 mL or 10 mL for 500 IU and 10 mL or 20 mL for 1000 IU). Do not use the water if beyond the expiry date or if signs of particulate matter are visible. Do not inject Sterilised Water for Injections, (Ph.Eur.), on its own.
The container of concentrate and the Sterilised Water for Injections, (Ph. Eur.), should be brought to between 20°C and 30°C, prior to the removal of the 'flip-off closures.
You can dissolve your product in two ways using the Transfer Device called Mix2Vial™:
(A) Dissolving in Full Volume or
(B) Dissolving with Half Volume
A) Dissolving in Full Volume
The Mix2VialTM Transfer Device is provided with the product for needle-free, easy and safe use.
Step 1: Remove the cap from the product vial and clean the top of the stopper with an alcohol swab. Repeat this step with the sterile water vial. Peel back the top of the Transfer Device package but leave the device in the package.
Step 2: Place the blue end of the Transfer Device on the water vial and push straight down until the spike penetrates the rubber stopper and snaps into place.
Remove the plastic outer packaging from the Transfer Device and discard it, taking care not to touch the exposed end of the device. Step 3: Turn the water vial upside down with the Transfer Device still attached.
Place the clear end of the Transfer Device on the product vial and push straight down until the spike penetrates the rubber stopper and snaps into place.
Step 4: The sterile water will be pulled into the product vial by the vacuum contained within it. Gently swirl the vial to make sure the product is thoroughly mixed. Do not shake the vial. A clear or slightly pearl-like solution should be obtained, usually in about 2 to 2 V minutes (5 minutes maximum).
Step 5: Separate the empty water vial and blue part from the clear part by
unscrewing anti-clockwise. Draw air into the syringe by pulling the plunger to the volume of water added. Connect the syringe to the white filter and push the air into the vial.
Step 6: Immediately invert the vial of solution which will be drawn into the syringe. Disconnect the filled syringe from the device. Follow normal safety practices to administer your medicine.
Note: If you have more than one vial to make up your dose, repeat Steps 1 through 6 withdrawing the solution in the vial into the same syringe.
The Transfer Device supplied with the product is sterile and cannot be used more than once. When the reconstitution process is complete dispose of in the ‘sharps box’.
B) Dissolving with Half Volume
This Transfer Device is provided with the product for easy and safe reconstitution.
• Firstly remove the cap from the Replenine-VF product vial and clean the top of the stopper with an alcohol swab. Repeat this step with the sterile water vial.
To use the Transfer Device for dissolving Replenine-VF in half volumes, it is first necessary to remove and discard half the water volume from the sterile water vial.
• Pierce the stopper of the sterile water vial with a needle and syringe and draw up half the volume of sterile water.
• Check that the correct amount is withdrawn, the needle and syringe can now be safely disposed of (in the ‘sharps box’).
• The remaining sterile water in the vial will be used for reconstitution (half the original volume).
• To complete the dissolving process, follow steps 1 to 6 in Section A above.
• The product is then ready for administration.
Any unused product or waste material should be disposed of in accordance with local requirements.
The solution should be clear or slightly opalescent. Do not use solutions that are cloudy or have deposits. Reconstituted products should be inspected visually for particulate matter and discolouration prior to administration.
7. MARKETING AUTHORISATION HOLDER
Bio Products Laboratory Limited
Dagger Lane
Elstree
Hertfordshire
WD6 3BX
United Kingdom.
8 MARKETING AUTHORISATION NUMBER(S)
PL 08801/0028
9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE
AUTHORISATION 9th August 1999
10 DATE OF REVISION OF THE TEXT
07/11/2012