<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"><channel><title><![CDATA[Celgene Corporation 보도자료 - 뉴스와이어]]></title><link>https://www.newswire.co.kr/?md=A10&amp;act=article&amp;no=21347></link><description><![CDATA[Celgene Corporation 보도자료 - 뉴스와이어 RSS 서비스]]></description><lastBuildDate>Fri, 01 May 2026 07:13:03 +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/2016/10/3554153577_20161014111817_3968656930.jpg]]></url></image><language>ko-KR</language><item><title><![CDATA[Data from Ozanimod Clinical Development Program in Relapsing Forms of Multiple Sclerosis to Be Presented at the 35th Congress of the European Committee for Treatment and Research in Multiple Sclerosis]]></title><link>https://www.newswire.co.kr/newsRead.php?no=893824</link><description><![CDATA[SUMMIT, N.J.--(Business Wire/Korea Newswire)--Celgene Corporation (NASDAQ:CELG) today announced it will present 13 scientific abstracts, including new analyses from the Phase 3 ozanimod clinical development program in adults with relapsing forms of multiple sclerosis (RMS), at the 35th Congress of the European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS) in Stockholm...]]></description><pubDate>Tue, 10 Sep 2019 09:04:48 +0900</pubDate></item><item><title><![CDATA[FDA Approves OTEZLA® (apremilast) for the Treatment of Oral Ulcers Associated with Behçet’s Disease]]></title><link>https://www.newswire.co.kr/newsRead.php?no=891543</link><description><![CDATA[SUMMIT, N.J.--(Business Wire/Korea Newswire)--Celgene Corporation (NASDAQ:CELG) today announced that the U.S. Food and Drug Administration (FDA) has approved OTEZLA® (apremilast) 30 mg twice daily (BID) for the treatment of adult patients with oral ulcers associated with Behçet’s Disease. OTEZLA, an oral, selective inhibitor of phosphodiesterase 4 (PDE4), is the first and only approved trea...]]></description><pubDate>Mon, 22 Jul 2019 14:43:12 +0900</pubDate></item><item><title><![CDATA[US FDA and EMA Accept Applications for Ozanimod for the Treatment of Relapsing Forms of Multiple Sclerosis]]></title><link>https://www.newswire.co.kr/newsRead.php?no=889461</link><description><![CDATA[SUMMIT, N.J.--(Business Wire/Korea Newswire)--Celgene Corporation (NASDAQ:CELG) today announced that the U.S. Food and Drug Administration (FDA) has accepted for review the New Drug Application for ozanimod for the treatment of people with relapsing forms of multiple sclerosis (RMS) in the United States. The European Medicines Agency (EMA) also accepted for review the Marketing Authorizatio...]]></description><pubDate>Mon, 10 Jun 2019 11:57:17 +0900</pubDate></item><item><title><![CDATA[Analysis Showed Oral Ozanimod Reduced Brain Volume Loss Across All Age Subgroups in Adults with Relapsing Multiple Sclerosis]]></title><link>https://www.newswire.co.kr/newsRead.php?no=887773</link><description><![CDATA[SUMMIT, N.J.--(Business Wire/Korea Newswire)--Celgene Corporation (NASDAQ:CELG) today announced the results of a post-hoc analysis of data from the Phase 3 RADIANCE™ Part B trial showing that ozanimod reduced cortical grey matter volume loss versus first-line treatment, Avonex® (interferon beta-1a), in adults with relapsing multiple sclerosis (RMS) across all age groups, including patients ...]]></description><pubDate>Wed, 08 May 2019 09:20:00 +0900</pubDate></item><item><title><![CDATA[Celgene Receives CHMP Positive Opinions for Both REVLIMID® (lenalidomide) and IMNOVID® (pomalidomide)-Based Triplet Combination Regimens for Patients with Multiple Myeloma]]></title><link>https://www.newswire.co.kr/newsRead.php?no=885808</link><description><![CDATA[SUMMIT, N.J.--(Business Wire/Korea Newswire)--Celgene Corporation (NASDAQ:CELG), today announced that the European Medicines Agency's (EMA) Committee for Medicinal Products for Human Use (CHMP) has adopted positive opinions for two triplet regimens based on Celgene’s proprietary IMiD® medications, REVLIMID (lenalidomide) and IMNOVID (pomalidomide).  The CHMP recommended approval of an expan...]]></description><pubDate>Mon, 01 Apr 2019 12:00:00 +0900</pubDate></item><item><title><![CDATA[Celgene Submits Application to FDA for Ozanimod for the Treatment of Relapsing Forms of Multiple Sclerosis]]></title><link>https://www.newswire.co.kr/newsRead.php?no=885444</link><description><![CDATA[SUMMIT, N.J.--(Business Wire/Korea Newswire)--Celgene Corporation (NASDAQ:CELG) today announced that the Company has submitted a New Drug Application to the U.S. Food and Drug Administration (FDA) for ozanimod for the treatment of adults with relapsing forms of multiple sclerosis (RMS). Ozanimod is an oral, sphingosine 1-phosphate (S1P) receptor modulator, which binds with high affinity sel...]]></description><pubDate>Tue, 26 Mar 2019 10:00:00 +0900</pubDate></item><item><title><![CDATA[Celgene Submits Application to EMA for Ozanimod for the Treatment of Relapsing-Remitting Multiple Sclerosis]]></title><link>https://www.newswire.co.kr/newsRead.php?no=884737</link><description><![CDATA[SUMMIT, N.J.--(Business Wire/Korea Newswire)--Celgene Corporation (NASDAQ:CELG) today announced that the Company has submitted a Marketing Authorization Application to the European Medicines Agency (EMA) for ozanimod for the treatment of adults with relapsing-remitting multiple sclerosis (RRMS). Ozanimod is an oral, sphingosine 1-phosphate (S1P) receptor modulator, which binds with high aff...]]></description><pubDate>Tue, 12 Mar 2019 10:40:00 +0900</pubDate></item><item><title><![CDATA[Celgene Corporation Announces Celgene Cancer Care Links™ Program Grant Recipients]]></title><link>https://www.newswire.co.kr/newsRead.php?no=880890</link><description><![CDATA[SUMMIT, N.J.--(Business Wire/Korea Newswire)--Celgene Corporation (NASDAQ:CELG) today announced ten programs selected for funding under its Celgene Cancer Care Links™ program, an initiative designed to support cancer healthcare capacity building in resource-constrained countries around the world.  The programs selected are expected to support established institutions partnering with in-coun...]]></description><pubDate>Tue, 18 Dec 2018 11:10:00 +0900</pubDate></item><item><title><![CDATA[Celgene Corporation Announces Initial Clinical Data from Ongoing Phase 1/2 Evolve Trial with Anti-BCMA CAR T Therapy JCARH125 in Relapsed/Refractory Multiple Myeloma at ASH 2018]]></title><link>https://www.newswire.co.kr/newsRead.php?no=880031</link><description><![CDATA[SUMMIT, N.J.--(Business Wire/Korea Newswire)--Celgene Corporation (NASDAQ:CELG) today announced initial safety data from its ongoing proof-of-concept trial of JCARH125 in patients with relapsed/refractory multiple myeloma. JCARH125 is an investigational BCMA-targeting CAR T cell therapy being developed by Juno Therapeutics, A Celgene Company. Results were presented by Sham Mailankody, MBBS,...]]></description><pubDate>Tue, 04 Dec 2018 10:35:00 +0900</pubDate></item><item><title><![CDATA[Celgene Corporation Announces Results of AUGMENT Evaluating REVLIMID® In Combination with Rituximab (R2) In Patients with Relapsed/Refractory Indolent Lymphoma At ASH 2018]]></title><link>https://www.newswire.co.kr/newsRead.php?no=879966</link><description><![CDATA[SUMMIT, N.J.--(Business Wire/Korea Newswire)--Celgene Corporation (NASDAQ: CELG) today announced results of the phase 3 AUGMENT study, which showed that REVLIMID® (lenalidomide) in combination with rituximab (R2) demonstrated superior progression-free survival (PFS) in patients with relapsed/refractory indolent lymphoma compared to patients who received rituximab plus placebo (R-placebo). T...]]></description><pubDate>Mon, 03 Dec 2018 14:25:00 +0900</pubDate></item><item><title><![CDATA[Celgene Corporation and Acceleron Pharma Announce Results of the Phase 3 MEDALIST Trial Evaluating Luspatercept in Patients with Myelodysplastic Syndromes at the ASH 2018 Plenary Session]]></title><link>https://www.newswire.co.kr/newsRead.php?no=879964</link><description><![CDATA[SUMMIT, N.J. & CAMBRIDGE, Mass.--(Business Wire/Korea Newswire)--Celgene Corporation (NASDAQ: CELG) and Acceleron Pharma Inc. (NASDAQ: XLRN) today announced results from the pivotal, phase 3 MEDALIST trial evaluating the efficacy and safety of investigational luspatercept to treat patients with ring sideroblast (RS+) myelodysplastic syndromes (MDS)-associated anemia who require red blood cell transfusions and...]]></description><pubDate>Mon, 03 Dec 2018 13:55:00 +0900</pubDate></item><item><title><![CDATA[Celgene Corporation Announces Initial Phase 1/2 Liso-cel Data in Patients with Relapsed/Refractory CLL, Including Those with High-Risk Disease, Previously Treated with Ibrutinib, at ASH 2018]]></title><link>https://www.newswire.co.kr/newsRead.php?no=879957</link><description><![CDATA[SUMMIT, N.J.--(Business Wire/Korea Newswire)--Celgene Corporation (NASDAQ: CELG) today announced initial data from the dose-escalation part of an ongoing, open-label multicenter phase 1/2 study of investigational lisocabtagene maraleucel (liso-cel; JCAR017) in patients with relapsed/refractory chronic lymphocytic leukemia (CLL) and small lymphocytic lymphoma (SLL), including patients with c...]]></description><pubDate>Mon, 03 Dec 2018 13:05:00 +0900</pubDate></item><item><title><![CDATA[Celgene Corporation and Acceleron Pharma Announce Results of the Phase 3 BELIEVE Trial Evaluating Luspatercept in Adult Patients with Beta-Thalassemia at ASH 2018]]></title><link>https://www.newswire.co.kr/newsRead.php?no=879956</link><description><![CDATA[SUMMIT, N.J. & CAMBRIDGE, Mass.--(Business Wire/Korea Newswire)--Celgene Corporation (NASDAQ: CELG) and Acceleron Pharma Inc. (NASDAQ: XLRN) today announced results from a pivotal, phase 3 trial (BELIEVE) evaluating the safety and efficacy of luspatercept for the treatment of adults with beta-thalassemia-associated anemia who require regular red blood cell (RBC) transfusions. The data were presented by Maria ...]]></description><pubDate>Mon, 03 Dec 2018 11:55:00 +0900</pubDate></item><item><title><![CDATA[New Analyses from Pivotal Phase 3 Trials of Oral Ozanimod to Be Presented at ECTRIMS 2018]]></title><link>https://www.newswire.co.kr/newsRead.php?no=876856</link><description><![CDATA[SUMMIT, N.J.--(Business Wire/Korea Newswire)--Celgene Corporation (NASDAQ:CELG) today announced the results of two post hoc analyses of data from the phase 3 SUNBEAM™ and RADIANCE™ Part B trials, which evaluated the efficacy and safety of ozanimod, a novel, oral, selective sphingosine 1-phosphate 1 (S1P1) and 5 (S1P5) receptor modulator, versus a first-line treatment, Avonex® (interferon be...]]></description><pubDate>Thu, 11 Oct 2018 15:50:00 +0900</pubDate></item><item><title><![CDATA[Celgene Announces Phase 3 STYLE Study of OTEZLA® (apremilast) in Moderate to Severe Scalp Psoriasis Met Primary Endpoint]]></title><link>https://www.newswire.co.kr/newsRead.php?no=876689</link><description><![CDATA[SUMMIT, N.J.--(Business Wire/Korea Newswire)--Celgene Corporation (NASDAQ:CELG) today announced results from the phase 3 STYLE study, which showed that OTEZLA® (apremilast) 30 mg twice daily achieved a highly statistically significant improvement in the primary endpoint of the Scalp Physician’s Global Assessment (ScPGA) response [defined as ScPGA score of clear (0) or almost clear (1) with ...]]></description><pubDate>Tue, 09 Oct 2018 10:35:00 +0900</pubDate></item><item><title><![CDATA[OTEZLA® (Apremilast) Showed Meaningful Improvements in Clinical and Quality-of-Life Measures of Psoriasis Beyond Those Captured by Assessing Skin Alone]]></title><link>https://www.newswire.co.kr/newsRead.php?no=875503</link><description><![CDATA[SUMMIT, N.J.--(Business Wire/Korea Newswire)--Celgene Corporation (NASDAQ:CELG) today announced the results of two post hoc sub-analyses of clinical trials for OTEZLA® (apremilast) at the 27th European Academy of Dermatology and Venereology (EADV) Congress in Paris, France. Findings suggest OTEZLA offered meaningful improvements in outcomes important to patients with moderate to severe plaq...]]></description><pubDate>Thu, 13 Sep 2018 10:10:00 +0900</pubDate></item><item><title><![CDATA[Celgene and Acceleron Announce Luspatercept Achieved Primary and All Key Secondary Endpoints in Phase III ‘BELIEVE’ Study in Adults with Transfusion-Dependent Beta-Thalassemia]]></title><link>https://www.newswire.co.kr/newsRead.php?no=872145</link><description><![CDATA[SUMMIT, N.J. & CAMBRIDGE, Mass.--(Business Wire/Korea Newswire)--Celgene Corporation (NASDAQ: CELG) and Acceleron Pharma Inc. (NASDAQ: XLRN) today announced results from a phase III, randomized, double-blind, multi-center clinical study (BELIEVE). Luspatercept achieved a highly statistically significant improvement in the primary endpoint of erythroid response, which was defined as at least a 33 percent reduc...]]></description><pubDate>Tue, 10 Jul 2018 11:05:00 +0900</pubDate></item><item><title><![CDATA[Results of Phase III RELEVANCE Study Comparing REVLIMID plus Rituximab (R2) Versus Rituximab Plus Chemotherapy in Patients with Previously Untreated Follicular Lymphoma to be Presented at ASCO 2018]]></title><link>https://www.newswire.co.kr/newsRead.php?no=870278</link><description><![CDATA[SUMMIT, N.J.--(Business Wire/Korea Newswire)--Celgene Corporation (NASDAQ:CELG) today announced additional results from RELEVANCE, a phase III, randomized, open-label, international clinical study conducted in partnership with the Lymphoma Academic Research Organisation (LYSARC), were presented at the 54th Annual American Society of Clinical Oncology Scientific Sessions (ASCO) in Chicago, I...]]></description><pubDate>Mon, 04 Jun 2018 14:00:00 +0900</pubDate></item><item><title><![CDATA[Results of Phase III OPTIMISMM Study Presented at ASCO 2018 Showed the PVd Triplet Improved PFS in Early Lines of Relapsed or Refractory Multiple Myeloma]]></title><link>https://www.newswire.co.kr/newsRead.php?no=870262</link><description><![CDATA[SUMMIT, N.J.--(Business Wire/Korea Newswire)--Celgene Corporation (NASDAQ:CELG) today announced results from the OPTIMISMM study, a phase III, randomized, open-label, international clinical study of the investigational combination regimen of POMALYST® (pomalidomide), bortezomib and dexamethasone in patients with relapsed or refractory multiple myeloma (RRMM) who had received at least one pr...]]></description><pubDate>Mon, 04 Jun 2018 11:50:00 +0900</pubDate></item><item><title><![CDATA[New Analyses from Pivotal Phase III Trials of Oral Ozanimod in Relapsing Multiple Sclerosis To Be Presented at the 2018 American Academy of Neurology Annual Meeting]]></title><link>https://www.newswire.co.kr/newsRead.php?no=868261</link><description><![CDATA[SUMMIT, N.J.--(Business Wire/Korea Newswire)--Celgene Corporation (NASDAQ:CELG) today announced additional phase III data analyses evaluating the efficacy and safety of ozanimod, a novel, oral, selective sphingosine 1-phosphate 1 (S1P1) and 5 (S1P5) receptor modulator, versus interferon beta-1a (IFN β-1a) (Avonex®) in patients with relapsing multiple sclerosis (RMS). These additional data a...]]></description><pubDate>Wed, 25 Apr 2018 11:20:00 +0900</pubDate></item><item><title><![CDATA[OTEZLA® (Apremilast) Phase III Data Showed Significant Improvements in Patients with Active Behçet’s Disease with Oral Ulcers]]></title><link>https://www.newswire.co.kr/newsRead.php?no=864710</link><description><![CDATA[SUMMIT, N.J.--(Business Wire/Korea Newswire)--Celgene Corporation (NASDAQ:CELG) today announced that data from the phase III RELIEF™ clinical trial of OTEZLA® (apremilast) in patients with active Behçet’s Disease with oral ulcers were presented in a late-breaking oral presentation at the 2018 American Academy of Dermatology (AAD) Annual Meeting. The results showed statistically significant ...]]></description><pubDate>Mon, 19 Feb 2018 11:20:00 +0900</pubDate></item><item><title><![CDATA[OTEZLA® (Apremilast) Phase II Data Showed Clinically Meaningful Improvements in Patients with Active Ulcerative Colitis]]></title><link>https://www.newswire.co.kr/newsRead.php?no=864706</link><description><![CDATA[SUMMIT, N.J.--(Business Wire/Korea Newswire)--Celgene Corporation (NASDAQ:CELG) announced that data from a randomized, placebo-controlled, multi-center, phase II clinical trial of apremilast in patients with active ulcerative colitis who had failed at least one conventional therapy but were naïve to biologic therapy were presented in an oral session today at the 13th Congress of ECCO in Vie...]]></description><pubDate>Mon, 19 Feb 2018 11:15:00 +0900</pubDate></item><item><title><![CDATA[Celgene Corporation and bluebird bio Announce Updated Results from Ongoing Multicenter Phase 1 Study of bb2121 Anti-BCMA CAR T Cell Therapy in Patients with Late Stage Relapsed/Refractory Multiple Myeloma at ASH Annual Meeting]]></title><link>https://www.newswire.co.kr/newsRead.php?no=861304</link><description><![CDATA[SUMMIT, N.J. & CAMBRIDGE, Mass.--(Business Wire/Korea Newswire)--Celgene Corporation (NASDAQ: CELG) and bluebird bio, Inc. (Nasdaq: BLUE) today announced that updated results from the ongoing CRB-401 Phase 1 clinical study of bb2121, an investigational anti-B-cell maturation antigen (BCMA) CAR T cell therapy, in 21 patients with late-stage relapsed/refractory multiple myeloma will be presented in an oral pres...]]></description><pubDate>Mon, 11 Dec 2017 09:20:00 +0900</pubDate></item><item><title><![CDATA[Celgene Corporation and bluebird bio Announce bb2121 Anti-BCMA CAR-T Cell Therapy Has Been Granted Breakthrough Therapy Designation from FDA and Prime Eligibility from EMA for Relapsed and Refractory Multiple Myeloma]]></title><link>https://www.newswire.co.kr/newsRead.php?no=859960</link><description><![CDATA[SUMMIT, N.J. & CAMBRIDGE, Mass.--(Business Wire/Korea Newswire)--Celgene Corporation (NASDAQ:CELG) and bluebird bio, Inc. (NASDAQ:BLUE) today announced that bb2121, a chimeric antigen receptor T-cell (CAR-T) therapy targeting b-cell maturation antigen (BCMA) in previously treated patients with multiple myeloma, has been granted Breakthrough Therapy Designation (BTD) by the U.S. Food and Drug Administration (F...]]></description><pubDate>Fri, 17 Nov 2017 09:55:00 +0900</pubDate></item><item><title><![CDATA[Efficacy and Safety Results from Second Phase III Trial (RADIANCE™ Part B) of Oral Ozanimod Versus an Active Comparator in Relapsing Multiple Sclerosis Presented at MSParis2017 - 7th Joint ECTRIMS - ACTRIMS Meeting]]></title><link>https://www.newswire.co.kr/newsRead.php?no=858730</link><description><![CDATA[SUMMIT, N.J.--(Business Wire/Korea Newswire)--Celgene Corporation (NASDAQ:CELG) today announced detailed results from the phase III RADIANCE™ Part B trial evaluating the efficacy and safety of ozanimod, a novel, oral, selective sphingosine 1-phosphate 1 (S1PR1) and 5 (S1PR5) receptor modulator, versus a first-line treatment, Avonex® (interferon beta-1a) (IFN), in patients with relapsing mul...]]></description><pubDate>Mon, 30 Oct 2017 10:00:00 +0900</pubDate></item></channel></rss>