<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"><channel><title><![CDATA[Biogen Idec 보도자료 - 뉴스와이어]]></title><link>https://www.newswire.co.kr/?md=A10&amp;act=article&amp;no=20987></link><description><![CDATA[Biogen Idec 보도자료 - 뉴스와이어 RSS 서비스]]></description><lastBuildDate>Thu, 14 May 2026 05:58:49 +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/2014/07/740813719_20140724102353_1178679641.jpg]]></url></image><language>ko-KR</language><item><title><![CDATA[Biogen Idec Presents Positive Interim Results from Phase 1B Study of Investigational Alzheimer’s Disease Treatment Aducanumab (BIIB037) at 2015 AD/PD™ Conference]]></title><link>https://www.newswire.co.kr/newsRead.php?no=786581</link><description><![CDATA[CAMBRIDGE, Mass.--(Business Wire/Korea Newswire)--Today Biogen Idec (NASDAQ:BIIB) announced data from a pre-specified interim analysis of PRIME, the Phase 1b study of aducanumab (BIIB037), in which aducanumab demonstrated an acceptable safety profile and positive results on radiologic and clinical measurements in patients with prodromal or mild Alzheimer’s disease (AD). These data are being pre...]]></description><pubDate>Mon, 23 Mar 2015 11:20:00 +0900</pubDate></item><item><title><![CDATA[PLEGRIDY™ (Peginterferon beta-1a) Approved in the European Union for the Treatment of Multiple Sclerosis]]></title><link>https://www.newswire.co.kr/newsRead.php?no=759785</link><description><![CDATA[CAMBRIDGE, Mass.--(Business Wire/Korea Newswire)--Today Biogen Idec (NASDAQ: BIIB) announced that the European Commission (EC) has granted marketing authorization for PLEGRIDYTM (peginterferon beta-1a) as a treatment for adults with relapsing-remitting multiple sclerosis (RRMS), the most common form of multiple sclerosis (MS). PLEGRIDY is dosed once every two weeks and is administered subcutane...]]></description><pubDate>Thu, 24 Jul 2014 10:20:00 +0900</pubDate></item><item><title><![CDATA[TECFIDERA® (Dimethyl Fumarate) Approved in the European Union as a First-Line Oral Treatment for Multiple Sclerosis]]></title><link>https://www.newswire.co.kr/newsRead.php?no=735633</link><description><![CDATA[CAMBRIDGE, Mass.--(Business Wire/Korea Newswire)--TECFIDERA® (dimethyl fumarate) has been approved by the European Commission (EC) as a first-line oral treatment for people with relapsing-remitting multiple sclerosis (RRMS), the most common form of multiple sclerosis (MS). Biogen Idec (NASDAQ: BIIB) will begin to introduce TECFIDERA in initial European Union (EU) countries in the coming weeks. ...]]></description><pubDate>Wed, 05 Feb 2014 14:10:00 +0900</pubDate></item><item><title><![CDATA[CHMP Determines Dimethyl Fumarate in TECFIDERA® to be a New Active Substance in the European Union]]></title><link>https://www.newswire.co.kr/newsRead.php?no=724820</link><description><![CDATA[CAMBRIDGE, Mass.--(Business Wire/Korea Newswire)--Today Biogen Idec (NASDAQ: BIIB) reported that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has determined that dimethyl fumarate in TECFIDERA qualifies as a new active substance (NAS). This designation will provide 10 years of regulatory exclusivity for TECFIDERA in the European Union (EU).   ...]]></description><pubDate>Mon, 25 Nov 2013 11:08:37 +0900</pubDate></item></channel></rss>