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| | Pegvisomant Basic information |
| | Pegvisomant Chemical Properties |
| | Pegvisomant Usage And Synthesis |
| Description | Acromegaly is a rare debilitating endocrine disease caused by the excessive secretion
of growth hormone (GH) and increased production of insulin-like growth factor I(IGF-I) in middle-aged adults. In over 90% of acromegaly patients, excess of GH is
associated with a benign pituitary adenoma. The clinical manifestations of
uncontrolled acromegaly include soft-tissue swelling, joint pain, nerve entrapment,
glucose intolerance, hypertension, and cardiac disease. Patients with acromegaly have
increased morbidity and mortality relative to the general population. The currently
available treatment options for acromegaly are surgical removal of the adenoma,
radiation therapy, and drug therapy with dopamine antagonists or somatostatin
analogues. Pegvisomant, launched as a new treatment for acromegaly, is a
modified form of human GH that acts as a highly selective GH receptor antagonist.
It is a PEGylated form of a recombinant human GH antagonist (B2036).
Pegvisomant selectively binds to GH receptors on cell surfaces, where it blocks
the binding of endogenous GH, and thus interferes with GH signal transduction. This
leads to a decrease in serum concentrations of IGF-I. A 12-week randomized,
double-blind, placebo-controlled clinical study found that daily treatment of
acromegaly patients with 10, 15, and 20 mg of pegvisomant resulted in normalized
IGF-I concentrations in 54, 81, and 89% of patients, respectively, compared to 10%
in the placebo group. An open-label extension study in which pegvisomant was
individually titrated demonstrated that 12-month or longer treatment resulted in
normalized IGF-I concentrations in 97% of patients. The recommended dosage
regimen of pegvisomant consists of a 40 mg loading dose, followed by 10 mg daily
dose, administered subcutaneously. The tmax of pegvisomant following SC administration is 33–77 h, with a bioavailability of 57% and t1/2 of six days.
Pegvisomant is generally well tolerated and the most common side effects include
injection-site reactions, diarrhea, nausea, chest pain and flu-like symptoms. | | Originator | Sensus (Pfizer) (US) | | Uses | Treatment
of acromegaly (competitive inhibition of peripheral growth
hormone receptors to block IFG-I production). | | Brand name | Somavert
(Pharmacia & Upjohn) [Note—The FDA has designated
pegvisomant (B2036-PEG) as an Orphan Drug for the
treatment of acromegaly.]. | | Biological Functions | This product contains 191 amino acid residues (of recombinant origin), the same number as in
GH, but there are substitutions at residues 18, 21, 120, 167, 168, 171, 172, 174, and 179. This
product is then covalently linked to several polyethylene glycol molecules, and this pegylated
protein is a GH-receptor antagonist. Thus, pegvisomant binds to the GH receptor and blocks
endogenous GH from binding. The result is a blocking of the GH-stimulated overproduction of
IGF-I that contributes to the disabling symptoms and long-term health problems associated with
acromegaly. |
| | Pegvisomant Preparation Products And Raw materials |
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