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Chong Kun Dang applied for Lucentis biosimilar

By Chon, Seung-Hyun | translator Choi HeeYoung

21.07.28 14:22:20

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Phase III demonstrated equivalence to the original


Chung Kun Dang announced on the 28th that it has applied to the MFDS for permission for the item of the macular denaturation drug CKD-701.

CKD-701(Ranibizumab) is a biosimilar product from Lucentis. Lucentis, sold by Roche and Novartis, is a drug used to treat ophthalmic diseases such as macular degenerative diabetes and macular edema. Lucentis' annual global sales amounted to about ₩4.6 trillion.

Chung Kun Dang confirmed clinical equivalence with Lucentis through phase 3 of CKD-701, which was conducted at 25 hospitals including Seoul National University from September 2018 to March this year for 312 patients with 312 patients with age-related macular degeneration.

Chung

Chon, Seung-Hyun(1000@dailypharm.com)
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