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Registration Date 23 Aug 2022
Revision Date 23 Aug 2022
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Mircera

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Medicine Pharmaceuticals

Anemia Drug

Drug Information

Generic
Methoxy polyethylene glycol-epoetin beta
Drug Class
Erythropoietin Receptor Activator
Therapeutic Class
Blood Modifiers
Dosage form
Solution
Route of Administration
SUBCUTANEOUS
Therapeutic Area
1.Anemia

Nanomaterials

Manufacturer Asserted

Polymeric Nanoparticle

Nanoparticle /Nanopowder

Benefit

Mircera or epoetin β (EPO) conjugated to methoxy-PEG is a drug formulation utilized in treatment of anemia. Mircera received its approval in 2007 by both European commission and the FDA. EPO is a genetically recombinant form of erythropoietin, which is capable of stimulating erythropoiesis by acting on the erythropoietin receptors of bone marrow progenitor cells. In Mircera, the PEG moiety (∼ 60 kD) is first linked with butanoic acid and the NHS modified structure is linked to the lysine moiety of the EPO structure via amide bonds. This formulation provides a controlled release system with a half-life of 135 h, in comparison with naked EPO with a half-life of 7–20 h. The main benefit is the less frequent administration when using Mircera. Administration of Mircera is through intravenous or subcutaneous injection of 0.6 μg/kg every 2 weeks.