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  • SCD's Eylea biosimilar was approved for phase III trials
  • by Lee, Tak-Sun | translator Choi HeeYoung | Sep 7, 2020 06:12am
The third domestic approval after Samsung Bioepis and Amgen, target for release in 2023
 ¡ã Eylea by Bayer
SCD Pharm has been approved for a phase III clinical trial of a biosimilar for Eylea (Aflibercept, Bayer), a macular degeneration treatment for the third time in Korea.

In June, it was approved for the third phase III clinical trial following Samsung Bioepis and Amgen. It is noted who will succeed in commercialization first in Korea. On the 2nd, the MFDS approved the multinational phase III clinical trial protocol of 'SCD411' applied by SCD Pharm.

This clinical trial is a phase III randomized, double-blind, parallel group, multicenter trial that compares efficacy, safety, tolerability, pharmacokinetics, and immunogenicity between SCD411 and Eylea in new vascular age-related macular degeneration test subjects.

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