<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"><channel><title><![CDATA[Celgene International Sàrl 보도자료 - 뉴스와이어]]></title><link>https://www.newswire.co.kr/?md=A10&amp;act=article&amp;no=23436></link><description><![CDATA[Celgene International Sàrl 보도자료 - 뉴스와이어 RSS 서비스]]></description><lastBuildDate>Mon, 04 May 2026 18:14:31 +0900</lastBuildDate><copyright>Copyright (c) 2004~2026 Korea Newswire All rights reserved</copyright><language>ko-KR</language><item><title><![CDATA[Celgene Receives Positive CHMP Opinion to Expand REVLIMID® (Lenalidomide) Indication as Monotherapy for the Maintenance Treatment of Patients with Newly Diagnosed Multiple Myeloma (MM) after Autologous Stem Cell Transplantation]]></title><link>https://www.newswire.co.kr/newsRead.php?no=844491</link><description><![CDATA[BOUDRY, Switzerland--(Business Wire/Korea Newswire)--Celgene International Sàrl, a wholly owned subsidiary of Celgene Corporation (NASDAQ:CELG), today announced that the European Medicines Agency's (EMA) Committee for Medicinal Products for Human Use (CHMP) has adopted a positive opinion for the use of REVLIMID® as monotherapy for the maintenance treatment of adult patients with newly diagnosed mu...]]></description><pubDate>Fri, 03 Feb 2017 10:10:00 +0900</pubDate></item><item><title><![CDATA[유럽 약물사용자문위원회(CHMP), 자가 조혈모세포이식술 후 다발성 골수종으로 새로 진단된 환자의 유지치료를 위한 단독요법으로 세엘진의 ‘레블리미드’(레날리도마이드)의 적응증을 확대하도록 긍정적 의견 채택]]></title><link>https://www.newswire.co.kr/newsRead.php?no=844492</link><description><![CDATA[부드리, 스위스--(Business Wire/뉴스와이어)--유럽의약청(EMA) 산하 약물사용자문위원회(CHMP)가 ‘레블리미드’(REVLIMID®)를 자가 조혈모세포이식(ASCT)술을 받은 후 다발성 골수종(MM)으로 새로 진단된 성인환자의 유지 치료를 위한 단독요법으로 사용할 수 있다는 긍정적인 의견을 채택했다고 세엘진 코퍼레이션(Celgene Corporation)(나스닥: CELG)의 완전 소유 자회사인 세엘진 인터내셔널(Celgene International Sà...]]></description><pubDate>Fri, 03 Feb 2017 10:10:00 +0900</pubDate></item><item><title><![CDATA[Oral Ozanimod Efficacy and Safety Results at 2 Years from Phase 2 RADIANCE Trial of Patients with Relapsing Multiple Sclerosis Presented at 32nd ECTRIMS]]></title><link>https://www.newswire.co.kr/newsRead.php?no=835410</link><description><![CDATA[BOUDRY, Switzerland--(Business Wire/Korea Newswire)--Celgene International Sàrl, a wholly owned subsidiary of Celgene Corporation (NASDAQ:CELG), today announced results from the 96-week blinded extension period (for a total of up to 120 weeks of exposure on treatment) of the RADIANCE phase 2 trial of ozanimod, an investigational oral, selective S1P 1 and 5 receptor modulator, in patients with rela...]]></description><pubDate>Mon, 19 Sep 2016 10:25:00 +0900</pubDate></item><item><title><![CDATA[Oral REVLIMID® Plus Dexamethasone Granted Approval for Treatment of Patients with Newly Diagnosed Multiple Myeloma in Japan]]></title><link>https://www.newswire.co.kr/newsRead.php?no=813319</link><description><![CDATA[BOUDRY, Switzerland & TOKYO--(Business Wire/Korea Newswire)--Celgene International Sàrl, a wholly-owned subsidiary of Celgene Corporation (NASDAQ:CELG) today announced that REVLIMID® (lenalidomide), a cancer medicine that is administered orally, has been granted full marketing authorization by Japan’s Ministry of Health, Labour and Welfare (MHLW) for use in combination with dexamethasone as a treatment fo...]]></description><pubDate>Mon, 21 Dec 2015 15:45:00 +0900</pubDate></item><item><title><![CDATA[One Year Data from Phase III Study Evaluating Oral OTEZLA® (apremilast) or Injectable etanercept versus Placebo in Patients with Moderate to Severe Plaque Psoriasis Presented at EADV]]></title><link>https://www.newswire.co.kr/newsRead.php?no=806090</link><description><![CDATA[BOUDRY, Switzerland--(Business Wire/Korea Newswire)--Celgene International Sàrl, a wholly owned subsidiary of Celgene Corporation (NASDAQ: CELG), today announced that results from its ongoing phase III LIBERATE™ trial evaluating Otezla® (apremilast), the Company’s oral, selective inhibitor of phosphodiesterase 4 (PDE4), in patients with moderate to severe plaque psoriasis were presented as a late-...]]></description><pubDate>Tue, 13 Oct 2015 09:50:00 +0900</pubDate></item><item><title><![CDATA[Celgene Announces New Data for OTEZLA® (Apremilast) Will Be Presented at European Academy of Dermatology and Venereology Congress]]></title><link>https://www.newswire.co.kr/newsRead.php?no=805944</link><description><![CDATA[BOUDRY, Switzerland--(Business Wire/Korea Newswire)--Celgene International Sàrl, a wholly-owned subsidiary of Celgene Corporation (NASDAQ:CELG), today announced that the latest research on Otezla® (apremilast), the Company's oral, selective inhibitor of phosphodiesterase 4 (PDE4), will be presented at the 24th European Academy of Dermatology and Venereology (EADV) Congress in Copenhagen, Denmark, ...]]></description><pubDate>Mon, 12 Oct 2015 09:25:00 +0900</pubDate></item><item><title><![CDATA[Celgene’s VIDAZA® (Azacitidine for Injection) Receives Positive CHMP Opinion as New Treatment for Elderly Patients with Acute Myeloid Leukaemia]]></title><link>https://www.newswire.co.kr/newsRead.php?no=804705</link><description><![CDATA[BOUDRY, Switzerland--(Business Wire/Korea Newswire)--Celgene International Sàrl, a wholly owned subsidiary of Celgene Corporation (NASDAQ: CELG) today announced that that the European Medicines Agency's (EMA) Committee for Medicinal Products for Human Use (CHMP) has adopted a positive opinion for an expanded indication of VIDAZA® (azacitidine for injection) for the treatment of adult patients aged...]]></description><pubDate>Fri, 25 Sep 2015 16:40:00 +0900</pubDate></item><item><title><![CDATA[ABRAXANE® Approved by European Commission for First-Line Treatment of Patients with Non-Small Cell Lung Cancer]]></title><link>https://www.newswire.co.kr/newsRead.php?no=784549</link><description><![CDATA[BOUDRY, Switzerland--(Business Wire/Korea Newswire)--Celgene International Sàrl, a wholly owned subsidiary of Celgene Corporation (NASDAQ: CELG), today announced that the European Commission (EC) has approved ABRAXANE® (paclitaxel formulated as albumin-bound nanoparticles, or nab-paclitaxel) in combination with carboplatin for the first-line treatment of non-small cell lung cancer in adult patient...]]></description><pubDate>Tue, 03 Mar 2015 17:00:00 +0900</pubDate></item><item><title><![CDATA[REVLIMID® (Lenalidomide) Approved by the European Commission for the Treatment of Adult Patients with Previously Untreated Multiple Myeloma who are Not Eligible for Transplant]]></title><link>https://www.newswire.co.kr/newsRead.php?no=783487</link><description><![CDATA[BOUDRY, Switzerland--(Business Wire/Korea Newswire)--Celgene International Sàrl, a wholly owned subsidiary of Celgene Corporation (NASDAQ: CELG), today announced that the European Commission (EC) has approved REVLIMID® (lenalidomide) for the treatment of adult patients with previously untreated multiple myeloma who are not eligible for transplant.  The REVLIMID Marketing Authorisation has been upd...]]></description><pubDate>Mon, 23 Feb 2015 11:55:00 +0900</pubDate></item><item><title><![CDATA[Celgene Receives Positive CHMP Opinion for ABRAXANE® for First-Line Treatment of Patients with Non-Small Cell Lung Cancer]]></title><link>https://www.newswire.co.kr/newsRead.php?no=781262</link><description><![CDATA[BOUDRY, Switzerland--(Business Wire/Korea Newswire)--Celgene International Sàrl, a wholly owned subsidiary of Celgene Corporation (NASDAQ: CELG), today announced that the European Medicines Agency's (EMA) Committee for Medicinal Products for Human Use (CHMP) has adopted a positive opinion for ABRAXANE® (paclitaxel formulated as albumin-bound nanoparticles, or nab-paclitaxel) in combination with ca...]]></description><pubDate>Wed, 28 Jan 2015 10:45:00 +0900</pubDate></item><item><title><![CDATA[Oral OTEZLA® (apremilast) Approved by the European Commission for the Treatment of both Patients with Psoriasis and Psoriatic Arthritis]]></title><link>https://www.newswire.co.kr/newsRead.php?no=780396</link><description><![CDATA[BOUDRY, Switzerland--(Business Wire/Korea Newswire)--Celgene International Sàrl (NASDAQ: CELG), a wholly-owned subsidiary of Celgene Corporation, today announced that the European Commission (EC) has granted marketing authorisation for OTEZLA® (apremilast), the company’s oral selective inhibitor of phosphodiesterase 4 (PDE4), in two therapeutic indications:[1]  · For the treatment of moderate-to-s...]]></description><pubDate>Mon, 19 Jan 2015 11:00:00 +0900</pubDate></item><item><title><![CDATA[Celgene Receives Positive CHMP Opinion to Extend REVLIMID® (Lenalidomide) for Continuous Use in Patients with Newly Diagnosed Multiple Myeloma and Ineligible for Transplant]]></title><link>https://www.newswire.co.kr/newsRead.php?no=778132</link><description><![CDATA[BOUDRY, Switzerland--(Business Wire/Korea Newswire)--Celgene International Sàrl, a wholly owned subsidiary of Celgene Corporation (NASDAQ: CELG), today announced that the European Medicines Agency's (EMA) Committee for Medicinal Products for Human Use (CHMP) has adopted a positive opinion for continuous oral treatment with REVLIMID® in adult patients with previously untreated multiple myeloma who ...]]></description><pubDate>Mon, 22 Dec 2014 13:35:00 +0900</pubDate></item><item><title><![CDATA[Phase II Data in Crohn’s Disease for Celgene’s Oral Antisense Therapy GED-0301 to Be Presented at UEG Week 2014]]></title><link>https://www.newswire.co.kr/newsRead.php?no=770606</link><description><![CDATA[BOUDRY, Switzerland--(Business Wire/Korea Newswire)--Celgene International Sàrl, a wholly-owned subsidiary of Celgene Corporation (NASDAQ:CELG), today announced that results from a double-blind, placebo-controlled, multicenter phase II trial of GED-0301 in 166 patients with active Crohn's disease will be presented at the United European Gastroenterology Week in Vienna, Austria.  The abstract title...]]></description><pubDate>Tue, 21 Oct 2014 13:05:00 +0900</pubDate></item><item><title><![CDATA[New Analyses of Oral OTEZLA® (Apremilast) Presented at EADV Show Efficacy in Difficult-to-Treat Areas of Moderate to Severe Plaque Psoriasis]]></title><link>https://www.newswire.co.kr/newsRead.php?no=769579</link><description><![CDATA[BOUDRY, Switzerland--(Business Wire/Korea Newswire)--Celgene International Sàrl, a wholly-owned subsidiary of Celgene Corporation (NASDAQ:CELG), today announced that results from additional efficacy and safety analyses of OTEZLA® (apremilast) from the ESTEEM phase III clinical trial program were released at the 23rd European Academy of Dermatology and Venereology (EADV) Congress in Amsterdam. Apre...]]></description><pubDate>Mon, 13 Oct 2014 11:40:00 +0900</pubDate></item><item><title><![CDATA[Oral OTEZLA® (apremilast) Data Presented at EADV Show Improved Measures of Health-Related Quality of Life and Work Productivity in Patients with Moderate to Severe Plaque Psoriasis]]></title><link>https://www.newswire.co.kr/newsRead.php?no=769577</link><description><![CDATA[BOUDRY, Switzerland--(Business Wire/Korea Newswire)--Celgene International Sàrl, a wholly-owned subsidiary of Celgene Corporation (NASDAQ: CELG) today announced that patient-reported health outcomes data for OTEZLA® (apremilast) were presented at the 23rd European Academy of Dermatology and Venereology (EADV) Congress in Amsterdam. The analyses from the phase III ESTEEM clinical trial program asse...]]></description><pubDate>Mon, 13 Oct 2014 11:35:00 +0900</pubDate></item></channel></rss>