<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"><channel><title><![CDATA[Amylyx Pharmaceuticals, Inc. 보도자료 - 뉴스와이어]]></title><link>https://www.newswire.co.kr/?md=A10&amp;act=article&amp;no=44176></link><description><![CDATA[Amylyx Pharmaceuticals, Inc. 보도자료 - 뉴스와이어 RSS 서비스]]></description><lastBuildDate>Mon, 04 May 2026 05:11:34 +0900</lastBuildDate><copyright>Copyright (c) 2004~2026 Korea Newswire All rights reserved</copyright><image><url><![CDATA[https://file.newswire.co.kr/data/upfile/company_img/2023/10/12_31017998_20231015111340_7529221869.jpg]]></url></image><language>ko-KR</language><item><title><![CDATA[Amylyx Pharmaceuticals Receives Negative CHMP Opinion on its Marketing Authorisation Application for AMX0035 for the Treatment of ALS in the European Union Following Re-Examination Process]]></title><link>https://www.newswire.co.kr/newsRead.php?no=976291</link><description><![CDATA[CAMBRIDGE, Mass--(Business Wire/Korea Newswire)--Amylyx Pharmaceuticals, Inc. (NASDAQ: AMLX) (“Amylyx” or the “Company”) today announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) confirmed its initial negative opinion on the Marketing Authorisation Application (MAA) for AMX0035 (sodium phenylbutyrate and ursodoxicoltaurine [also known...]]></description><pubDate>Sun, 15 Oct 2023 11:32:07 +0900</pubDate></item></channel></rss>