Elosulfase alfa

DB09051

biotech approved investigational

Deskripsi

Elosulfase alfa is a synthetic version of the enzyme N-acetylgalactosamine-6-sulfatase. It was approved by the FDA in 2014 for the treatment of Morquio syndrome. Elosulfase alfa was developed by BioMarin Pharmaceutical Inc. and is marketed under the brand Vimizim™. The recommended dose is 2 mg per kg given intravenously over a minimum range of 3.5 to 4.5 hours, based on infusion volume, once every week.

Struktur Molekul 2D

Struktur tidak tersedia

Peta Jejaring Molekuler
Legenda: ObatTargetGenEnzim(Panah → menunjukkan arah efek / relasi)TransporterCarrier

Profil Farmakokinetik

Waktu Paruh (Half-Life) week 0: 7.52 min week 22: 35.9 min
Volume Distribusi 396 mL/kg, standard deviation 316.
Klirens (Clearance) 10.0 mL/min/kg. (standard deviation: 3.73).

Absorpsi

Cmax: 1.49 ?g/mL, standard deviation 0.534.

Metabolisme

Data metabolisme tidak tersedia.

Rute Eliminasi

Data eliminasi belum tersedia.

Interaksi Obat

0 Data
Tidak ada data.

Referensi & Sumber

Artikel (PubMed)
  • PMID: 24700469
    Sanford M, Lo JH: Elosulfase alfa: first global approval. Drugs. 2014 Apr;74(6):713-8. doi: 10.1007/s40265-014-0210-z.

Contoh Produk & Brand

Produk: 2 • International brands: 0
Produk
  • Vimizim
    Injection, solution, concentrate • 5 mg/5mL • Intravenous • US • Approved
  • Vimizim
    Solution • 1 mg / mL • Intravenous • Canada • Approved

Sekuens Gen/Protein (FASTA)

Sekuens dimuat saat dibutuhkan agar halaman tetap ringan.
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