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Stelfonta - patient leaflet, side effects, dosage

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Patient leaflet - Stelfonta

B. PACKAGE LEAFLET

PACKAGE LEAFLET:

STELFONTA 1 mg/ml solution for injection for dogs

  • 1. NAME AND ADDRESS OF THE MARKETING AUTHORISATION HOLDER AND OF THE MANUFACTURING AUTHORISATION HOLDER RESPONSIBLE FOR BATCH RELEASE, IF DIFFERENT

Marketing authorisation holder :

QBiotics Netherlands B.V.

Prinses Margrietplantsoen 33

2595 AM The Hague

Netherlands

Manufacturer responsible for batch release :

Virbac

1ère avenue

2065m L I D

06516 Carros

France

  • 2. NAME OF THE VETERINARY MEDICINAL PRODUCT

STELFONTA 1 mg/ml solution for injection for dogs

Tigilanol tiglate

  • 3. STATEMENT OF THE ACTIVE SUBSTANCE(S) AND OTHER INGREDIENT(S)

Each ml contains:

Active substance:

Tigilanol tiglate 1 mg

  • 4. INDICATION(S)

For the treatment of non-resectable, non-metastatic (WHO staging) subcutaneous mast cell tumours located at or distal to the elbow or the hock, and non-resectable, non-metastatic cutaneous mast cell tumours in dogs. Tumours must be less than or equal to 8 cm3 in volume, and must be accessible to intratumoral injection.

  • 5. CONTRAINDI­CATIONS

In order to minimise product leakage from the tumour surface upon injection, do not use in mast cell tumours with a broken surface.

Do not administer the product directly into the surgical margins following the surgical removal of a tumour.

  • 6. ADVERSE REACTIONS

Manipulation of mast cell tumours may cause the tumour cells to degranulate. Degranulation can result in swelling and redness at and around the tumour site as well as systemic clinical signs, including stomach ulceration and bleeding and potentially life-threatening complications, including hypovolemic shock and/or a systemic inflammatory response. In order to reduce the occurrence of local and systemic adverse events related to mast cell degranulation and histamine release, all treated dogs must be provided with concomitant supportive therapies, consisting of corticosteroids and H1 and H2 receptor blocking agents, both before and after treatment.

Formation of wounds is an intended reaction to treatment and is expected following the use of this veterinary medicinal product in all cases. In the pivotal field study, a maximum wound surface area was observed at 7 days after treatment for most patients, although in a small number of cases wound size increased up to 14 days post treatment. Most wounds were completely re-epithelised within 28 to 42 days of treatment (with individual cases that healed by day 84. In most cases, the wound area will increase with increasing tumour size.. However, this is not a reliable predictor for wound size or severity and duration of healing. These wounds resolve by second intention healing with minimal intervention. Wound management measures may be required as deemed necessary by the responsible veterinarian. The speed of healing is related to the size of the wound.

Commonly reported local adverse events, such as pain, injection site bruising/eryt­hema/oedema, lameness in a treated limb and wound formation, are related to localised pathology. The wounds may evolve to cover significantly larger areas than the original size of the tumour.

Very common

Mild to moderate:

Pain upon injection.

Wound formation at the injection site, associated with pain and lameness.

Vomiting and tachycardia.

Common

Severe:

Lameness, pain, wound formation at the injection site and scar contraction. Lethargy.

Mild to moderate:

Enlargement of draining lymph node, wound infection, bruising, erythema and oedema.

Diarrhoea, anorexia, weight loss, tachypnoea, lethargy, pyrexia, cystitis, reduced appetite, new neoplastic mass, personality/be­haviour changes, pruritis, tremor and skin ulceration.

Anaemia, neutrophilia, increased band neutrophils, hypoalbuminemia, leucocytosis, monocytosis, and elevated creatine kinase.

Uncommon

Severe:

Infection/cellu­litis, wound slough.

Anorexia, reduced appetite, somnolence, tachycardia, neuropathy and pruritis. Leucocytosis, increased band neutrophils, thrombocytopenia and elevated ALT. Seizures.

Mild to moderate:

Formation of a transient peri-wound nodule.

Dehydration, haemorrhage, cholestasis, polydipsia, polyuria, regurgitation, melaena, flatulence, urinary incontinence, inappropriate defecation, maculopapular rash, abrasion, dermatitis, licking, restlessness.

Proteinuria, thrombocytosis, elevated ALT and ALP, elevated bilirubin, elevated BUN, elevated GGT, elevated triglyceride, and hyperkalaemia.

The frequency of adverse reactions is defined using the following convention: – very common (more than 1 in 10 animals treated displaying adverse reaction(s)) – common (more than 1 but less than 10 animals in 100 animals treated) – uncommon (more than 1 but less than 10 animals in 1,000 animals treated) – rare (more than 1 but less than 10 animals in 10,000 animals treated) – very rare (less than 1 animal in 10,000 animals treated, including isolated reports).

If you notice any side effects, even those not already listed in this package leaflet or you think that the medicine has not worked, please inform your veterinary surgeon.

  • 7. TARGET SPECIES

Dogs

  • 8. DOSAGE FOR EACH SPECIES, ROUTE(S) AND METHOD OF ADMINISTRATION

STELFONTA is provided as a single use vial for intratumoral (IT) injection.

The surface of the mast cell tumour (MCT) to be treated must be intact, with the expectation of minimal product leakage from the tumour surface after IT injection.

Before administering this veterinary medicinal product, it is essential that concomitant treatments (corticosteroids, H1 and H2 receptor blocking agents) are initiated to address the risk of mast cell degranulation. See ‚concomitant treatment‘ below.

Administer the veterinary medicinal product as a single dose of 0.5 ml per cm3 of tumour volume, as determined on the day of dosing (following initiation of concomitant treatments) by the equations below:

Calculate the tumour size:

Tumour Volume (cm3) = 4 (length (cm) x width (cm) x height (cm))

Calculate the dose:

Dose volume of STELFONTA (ml) to inject = Tumour Volume (cm3) x 0.5

The maximum dose of the veterinary medicinal product is 0.15 ml/kg body weight (corresponding to 0.15 mg tigilanol tiglate/kg bw), with no more than 4 ml administered per dog, regardless of the number of tumours treated, the tumour volume or the dog’s body weight.

The minimum dose of the veterinary medicinal product is 0.1 ml, regardless of the tumour volume or the dog’s body weight.

  • 9. ADVICE ON CORRECT ADMINISTRATION

Appropriate hygienic measures (such as clipping of the treated area) should be performed prior to treatment.

Once the correct dose of the veterinary medicinal product has been determined, draw the required volume into a sterile Luer lock syringe with a 23–27 gauge needle.

Caution should be used to avoid manipulation of the tumour to minimise the risk of degranulation. To inject, insert the needle into the tumour mass through a single injection site. Whilst applying even pressure on the syringe plunger, move the needle back and forth in a fanning manner to inject the veterinary medicinal product into different locations within the tumour. Care should be taken to restrict injections to the tumour mass only (no injection into the margins or beyond the periphery of the tumour).

When the total dose of the veterinary medicinal product has been administered, pause for up to 5 seconds to allow tissue dispersion before removing the needle from the tumour.

The site of application should be covered for the first day after treatment in order to prevent direct contact with residual or leaking product. Handle the cover with gloves to avoid contact with the product. In case of severe leakage of wound debris, which may occur in the first weeks following administration of the product, the wound should be covered.

If tumour tissue remains 4 weeks after the initial treatment and the surface of the residual mass is intact, a second dose may be administered. The size of the residual tumour should be measured and the new dose calculated before the second dose is administered.

Concomitant treatment

The following medications must be given concurrently with each treatment with STELFONTA to address the potential for mast cell degranulation:

Corticosteroids (oral prednisone or prednisolone): start treatment 2 days prior to the treatment with STELFONTA at a total dose of 1 mg/kg, administered at 0.5 mg/kg orally, twice a day (PO BID), and continue daily until 4 days post-treatment (i.e. for 7 days in total). Then reduce the corticosteroid dose to a single dose of 0.5 mg/kg orally, once a day (PO OID) for a further 3 days.

H1 and H2 receptor blocking agents: start treatment on the day of administration of STELFONTA and continue for 8 days.

  • 10. WITHDRAWAL PERIOD(S)

Not applicable.

  • 11. SPECIAL STORAGE PRECAUTIONS

Keep out of sight and reach of children.

Store in a refrigerator (2°C – 8°C).

Do not freeze.

Keep the vial in the outer carton in order to protect from light.

Once broached, use immediately.

Do not use this veterinary medicinal product after the expiry date which is stated on the label or carton after „EXP“. The expiry date refers to the last day of that month.

  • 12. SPECIAL WARNING(S)

Special warnings for each target species:

The effect of STELFONTA on mast cell tumours is restricted to the location of injection, as it is not systemically active. STELFONTA should therefore not be used in case of metastatic disease. Treatment does not prevent the development of de novo mast cell tumours. Treatment causes a change in the tissue architecture. It is therefore unlikely that an accurate histological tumour grading can be obtained after treatment.

Special precautions for use in animals:

The product must strictly be administered intratumorally, as other routes of injections are associated with adverse reactions. Unintentional intravenous (IV) administration should be avoided at all times, since this is expected to cause severe systemic effects.

After injection of tigilanol tiglate into the subcutaneous tissues, even at low concentration­s/doses, treated dogs exhibited restlessness and vocalisation, as well as severe local reactions at the injection sites. Injection into non-neoplastic tissues can cause a transient, local response resulting in localised inflammation, oedema, redness and pain. Cases of wound formation have been observed following subcutaneous injection of tigilanol tiglate.

Treatment induces a substantial local inflammatory reaction, generally lasting up to approximately 7 days. Consideration should be given to providing additional analgesia if required, based on clinical assessment by the veterinarian. Any bandaging used must be loose to allow for anticipated local oedema.

Treating tumours in mucocutaneous locations (eyelids, vulva, preputial opening, anus, mouth) and at the extremities (e.g. paws, tail) could impair functionality due to the loss of tissue associated with the treatment.

The product is an irritant; therefore, use of the product in the proximity of sensitive tissues, in particular the eye, should be avoided.

In order to reduce the occurrence of local and systemic adverse events related to mast cell degranulation and histamine release, all treated dogs must be provided with concomitant supportive therapies, consisting of corticosteroids and H1 and H2 receptor blocking agents, both before and after treatment.

Owners should be advised to check for signs of potential mast cell degranulation reactions. These include vomiting, anorexia, severe pain, lethargy, inappetence or extensive swelling. If signs of degranulation are observed, the treating veterinarian should be contacted straight away, so that appropriate treatment can be started immediately.

Following treatment, drinking water should always be available.

The safety of the product has not been established in dogs that are less than 12 months of age.

Tumours that lie completely in the subcutaneous tissue with no dermal involvement may have difficulty in creating an exit site for necrotic tissue removal. This may necessitate an incision to allow for drainage of necrotic tissue.

The product is to be administered only by a veterinarian.

Special precautions to be taken by the person administering the veterinary medicinal product to animals:

Special precautions to be taken by the professional user (veterinarian):

Veterinarians should inform the pet owner about the special precautions to be taken at home.

People with known hypersensitivity to tigilanol tiglate or to propylene glycol should avoid contact with the product. The product is an irritant and potentially a skin sensitiser.

Accidental self-injection may result in severe local inflammatory reactions, including pain, swelling, redness and potential wound formation/necrosis, which may take several months to resolve. Caution is required during treatment to avoid self-injection. Dogs undergoing treatment with the product should be adequately restrained, including by sedation if necessary. Use a Luer lock syringe to administer the product. In case of accidental self-injection, seek medical advice immediately and show the package insert to the physician.

Accidental exposure to skin, eye, or by ingestion should be avoided. Leakage of the product from the site of injection may occur directly after administration. Personal protective equipment consisting of disposable impervious gloves and protective eye glasses should be worn when handling the product and/or touching the site of injection. In case of dermal or ocular exposure, repeatedly wash the exposed skin or eye with water. If symptoms such as local signs of redness and swelling occur, or if there has been ingestion, seek the advice of a physician and show them the package leaflet.

The safety of the veterinary medicinal product has not been established during pregnancy or lactation. Pregnant women and breastfeeding women should take care to avoid accidental self-injection, contact with the injection site, leaking product and tumour debris.

Special precautions to be taken by the animal owner:

Low levels of tigilanol tiglate residues might be present in the wound debris. In case of severe leakage of wound debris, which may occur in the first weeks following administration of the product, the wound should be covered. If however covering the wound is contraindicated due to its healing, the dog must be kept away from children. Wound debris should only be handled with protective equipment (disposable gloves).

In case of any contact with wound debris, the affected area(s) on the person should be thoroughly washed. Contaminated areas or bedding should be thoroughly cleaned/washed.

The safety of the veterinary medicinal product has not been established during pregnancy or lactation. Pregnant women and breastfeeding women should take care to avoid contact with the injection site, leaking product and tumour debris.

Pregnancy, lactation and fertility :

The safety of the veterinary medicinal product has not been established during pregnancy or lactation or in dogs intended for breeding. The use of the veterinary medicinal product is therefore not recommended in these animals.

Interaction with other medicinal products and other forms of interaction:

None known.

No specific interaction studies have been performed with the veterinary medicinal product, but in field trials no interactions were observed when administered concomitantly with corticosteroids (prednisone / prednisolone) and H1 and H2 receptor blocking agents (e.g. diphenhydramine / chlorpheniramine and famotidine), or with opioid analgesics (e.g. tramadol hydrochloride).

The concomitant use of non-steroidal anti-inflammatory drugs (NSAIDs) has not been investigated in the pivotal clinical trial, as they are not recommended for concomitant use with corticosteroids.

Overdose (symptoms, emergency procedures, antidotes) :

In a laboratory safety study conducted in young healthy male Beagle dogs, overdose signs such as vomiting were observed following a 15 minute intravenous infusion of 0.05 mg tigilanol tiglate/kg b.w. Further signs such as swaying gait, tachypnoea and lateral position occurred following a 15 minute intravenous infusion at a dose rate of 0.10–0.15 mg/kg b.w. These signs were severe, but selflimiting. Apathy, mydriasis, seizures and finally death were seen following a 15 minute intravenous infusion with 0.225 mg/kg b.w.

There is no known antidote for overdosage of STELFONTA. In case of adverse events during or following overdosage, supportive treatment should be administered at the discretion of the attending veterinarian.

  • 13. SPECIAL PRECAUTIONS FOR THE DISPOSAL OF UNUSED PRODUCT OR WASTE MATERIALS, IF ANY

Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal products should be disposed of in accordance with local requirements.

  • 14. DATE ON WHICH THE PACKAGE LEAFLET WAS LAST APPROVED

Detailed information on this veterinary medicinal product is available on the website of the European Medicines Agency.

  • 15. OTHER INFORMATION