Active Ingredient: Lanreotide
Lanreotide is indicated for the treatment of grade 1 and a subset of grade 2 (Ki67 index up to 10%) gastroenteropancreatic neuroendocrine tumours (GEP-NETs) of midgut, pancreatic or unknown origin where hindgut sites of origin have been excluded, in adult patients with unresectable locally advanced or metastatic disease.
For this indication, competent medicine agencies globally authorize below treatments:
For:
Subcutaneous, 120 milligrams lanreotide, once every 28 days.
The recommended dose is one injection of lanreotide 120 mg administered every 28 days.
The treatment with lanreotide should be continued for as long as needed for tumour control.
Lanreotide is administered by deep subcutaneous injection in the superior external quadrant of the buttock or in the upper outer thigh.
For patients who receive a stable dose of lanreotide, and after appropriate training, the injection may be administered either by the patient or by a trained person. In case of self-injection, the injection should be given in the upper outer thigh.
The decision regarding administration by the patient or a trained person should be taken by a healthcare professional.
Regardless of the injection site, the skin should not be folded and the needle should be inserted rapidly and to its full length, perpendicularly to the skin.
The injection site should alternate between the right and left side.
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