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'Vabysmo¡¯s 4mth dosing interval may reduce patient burden'

By Jung, Sae-Im | translator Kim, Jung-Ju

23.03.07 16:23:01

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Roche Korea holds press conference to celebrate Vabysmo¡¯s approval in Korea

First bispecific antibody in ophthalmology...only drug that inhibits the disease factor angiopoietin-2

¡°Patients experience high burden due to every 4-8 week administration...Vabysmo will offer an alternative for these patients¡±

A new drug for Neovascular (Wet) Age-Related Macular Degeneration (nAMD) that offers treatment effect with once every 4-month administration has landed in Korea. The new option is expected to greatly improve the convenience of administration in domestic patients whose number has been increasing with Korea¡¯s aging population.

Roche Korea held a press conference on the 7th to celebrate the approval of Vabysmo (faricimab) at its headquarters in Seocho-gu, Seoul.

Vabysmo is the first bispecific antibody that targets both the VEGF that is commonly targeted by existing ocular disease treatments as well as angiopoietin-2 (Ang-2) that are considered to be the cause of retinal disease to block both

Jung, Sae-Im (same@dailypharm.com)
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