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Bayer/RegeneronÀÇ Eylea¿¡ ´ëÇ×ÇÑ Roche VabysmoÀÇ µµÀÔ¿¡ ÀÇÇØ Á¦ÀÏ ¼±ÅþàÀÇ ¼¼·Âµµ´Â ¹Ù²î°í ÀÖ½À´Ï´Ù. ÇÑÆí, ÀûÀÀ¿Ü ¾Æ¹Ù½ºÆ¾Àº ¿©ÀüÈ÷ ºñ¿ë È¿°ú°¡ ³ôÀº ¿É¼ÇÀ̳ª, »õ·Î¿î Áøº¸¿¡ ÀÇÇØ »ç¿ëÀº °¨¼ÒÇÒÁöµµ ¸ð¸¨´Ï´Ù. ¹Ì·¡¸¦ Àü¸ÁÇϸé Ä¡·á °£°ÝÀÇ ¿¬Àå, ½Ã·ÂÀÇ °³¼±, ħ½ÀÀÌ ÀûÀº ¿É¼Ç¿¡ ÃÊÁ¡À» ¸ÂÃâ ¼ö ÀÖÀ¸¸ç, À¯ÀüÀÚ Ä¡·á, Ƽ·Î½Å Å°³ª¾ÆÁ¦ ÀúÇØÁ¦, D 4517.2 ¹× Axpaxli¿Í °°Àº Çõ½ÅÀûÀÎ ¾àÁ¦ÀÇ °¡´É¼ºÀÌ °Á¶µÇ°í ÀÖ½À´Ï´Ù. ¹ÌÃæÁ· ¿ä±¸¿¡ ´ëÇÑ ´ëÀÀ°ú ½Å±Ô Ä¡·á °æ·ÎÀÇ Ã¤ÅÃÀ» ÇâÇÑ Àü·«Àû ÃàÀÌ wAMD Ä¡·á¿¡¼ ÀÌ ¸Å¿ì Áß¿äÇÑ ½Ã±â¿¡ ¿ä±¸µÇ°í ÀÖ½À´Ï´Ù.
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With the introduction of Roche's Vabysmo challenging Bayer/Regeneron's Eylea, the dynamics of first-line choices are shifting. Meanwhile, off-label Avastin remains a cost-effective option, though its usage may wane with new advancements. As we look to the future, the focus sharpens on longer treatment intervals, improved visual acuity, and less invasive options, highlighting the potential of gene therapies, tyrosine kinase inhibitors, and innovative drugs like D 4517.2 and Axpaxli. This pivotal moment in wAMD treatment calls for a strategic pivot towards addressing unmet needs and embracing novel therapeutic pathways.