Acromegaly

Active Ingredient: Pasireotide

Indication for Pasireotide

Population group: only adults (18 years old or older)

Treatment of adult patients with acromegaly for whom surgery is not an option or has not been curative and who are inadequately controlled on treatment with another somatostatin analogue.

For this indication, competent medicine agencies globally authorize below treatments:

40-60 mg once every 4 weeks

Route of admnistration

Subcutaneous

Defined daily dose

40 - 60 mg

Dosage regimen

From 40 To 60 mg once every 28 day(s)

Detailed description

The recommended initial dose for the treatment of acromegaly is 40 mg of pasireotide every 4 weeks.

The dose may be increased to a maximum of 60 mg for patients whose growth hormone (GH) and/or insulin-like growth factor-1 (IGF-1) levels are not fully controlled after 3 months of treatment with pasireotide at 40 mg.

Management of suspected adverse reactions or over-response to treatment (IGF-1 < lower limit of normal) may require temporary dose reduction of pasireotide. The dose may be decreased either temporarily or permanently.

Missed dose

If a dose of pasireotide is missed the missed injection should be administered as soon as possible. The next dose should then be planned for 4 weeks after the injection is administered in order to resume the normal schedule of one dose every 4 weeks.

Dosage considerations

The site of repeat intramuscular injections should be alternated between the left and right gluteal muscle.

Active ingredient

Pasireotide

Pasireotide is a novel cyclohexapeptide, injectable somatostatin analogue. Pasireotide exerts its pharmacological activity via binding to somatostatin receptors. Somatostatin receptors are expressed in many tissues, especially in neuroendocrine tumours in which hormones are excessively secreted, including ACTH in Cushing’s disease.

Read more about Pasireotide

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