<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"><channel><title><![CDATA[EUSA Pharma 보도자료 - 뉴스와이어]]></title><link>https://www.newswire.co.kr/?md=A10&amp;act=article&amp;no=31226></link><description><![CDATA[EUSA Pharma 보도자료 - 뉴스와이어 RSS 서비스]]></description><lastBuildDate>Sat, 02 May 2026 20:37:14 +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/2018/07/3698601005_20180712155316_8663944742.jpg]]></url></image><language>ko-KR</language><item><title><![CDATA[EUSA Pharma Announces FDA Approval of Phase 3 Clinical Trial for Siltuximab in Hospitalized Patients With COVID-19 Associated Acute Respiratory Distress Syndrome]]></title><link>https://www.newswire.co.kr/newsRead.php?no=907335</link><description><![CDATA[HEMEL HEMPSTEAD, United Kingdom & BURLINGTON, Mass--(Business Wire/Korea Newswire)--EUSA Pharma, a global biopharmaceutical company focused on oncology and rare disease, today announced that the U.S. Food &amp; Drug Administration (FDA) has approved a randomized, double-blind, placebo-controlled Phase 3 clinical trial protocol to evaluate the safety and efficacy of intravenous siltuximab plus standard of care in hospitalized pa...]]></description><pubDate>Fri, 03 Jul 2020 14:00:00 +0900</pubDate></item><item><title><![CDATA[EUSA 파마, 코비드 19와 관련된 급성호흡곤란증후군 입원환자들에 대해 FDA로부터 실툭시맙 3상 임상시험 승인받아]]></title><link>https://www.newswire.co.kr/newsRead.php?no=907337</link><description><![CDATA[헤멜 헴스테드, 영국/벌링턴, 매사추세츠--(Business Wire/뉴스와이어)--종양학과 희귀질환에 중점을 둔 글로벌 바이오 제약회사 EUSA 파마(EUSA Pharma)가 코비드 19(COVID-19)와 관련된 급성호흡곤란증후군(ARDS)으로 인해 입원한 환자들에 대해 실툭시맙(siltuximab) 플러스 정맥주사 표준치료를 하는 데 대해 미국 식품의약국(FDA)이 무작위배정, 이중맹검, 위약대조 3상 임상시험 프로토콜을 승인했다고 2일 발표했다.  실툭시맙은 코비드 19...]]></description><pubDate>Fri, 03 Jul 2020 14:00:00 +0900</pubDate></item><item><title><![CDATA[EUSA파마와 이탈리아의 파파 지오바니 23 병원, COVID-19 환자를 실툭시맙으로 치료한 SISCO 연구의 중간 분석 데이터 발표]]></title><link>https://www.newswire.co.kr/newsRead.php?no=903305</link><description><![CDATA[헤멜 헴스테드, 영국/베르가모, 이탈리아--(Business Wire/뉴스와이어)--종양학과 희귀질환에 중점을 둔 글로벌 바이오 제약회사인 EUSA파마(EUSA Pharma)가 2020년 3월 24일 미리 계획한 데이터 분석을 바탕으로 파파 지오바니 23 병원(Papa Giovanni XXIII Hospital)이 후원해 실시한 SISCO(Siltuximab In Serious COVID-19, 중증 코로나바이러스 감염증-19에 대한 실툭시맙 사용) 연구[1] 1차 예비 결과를 1일 발표했다.      실툭시맙은 인체 ...]]></description><pubDate>Thu, 02 Apr 2020 14:16:08 +0900</pubDate></item><item><title><![CDATA[EUSA Pharma and Papa Giovanni XXIII Hospital, Italy, Provide Interim Analysis Data for Siltuximab-Treated COVID-19 Patients from the SISCO Study]]></title><link>https://www.newswire.co.kr/newsRead.php?no=903301</link><description><![CDATA[HEMEL HEMPSTEAD, United Kingdom & BERGAMO, Italy--(Business Wire/Korea Newswire)--EUSA Pharma, a global biopharmaceutical company focused on oncology and rare disease, today announced initial preliminary findings from the Papa Giovanni XXIII Hospital sponsored SISCO (Siltuximab In Serious COVID-19) Study,[1] based on a pre-planned data analysis on 24 March 2020.  Siltuximab is an interleukin (IL)-6 targeted monoclonal antibod...]]></description><pubDate>Thu, 02 Apr 2020 14:11:48 +0900</pubDate></item><item><title><![CDATA[EUSA 파마와 이탈리아 베르가모 소재 파파 지오바니 23 병원, 코로나19 환자들 중 심각한 호흡기 합병증을 일으킨 환자들 대상 실툭시맙 환자-대조군 관찰 연구 착수했다고 발표]]></title><link>https://www.newswire.co.kr/newsRead.php?no=902711</link><description><![CDATA[헤멜 헴스테드, 영국/베르가모, 이탈리아--(Business Wire/뉴스와이어)--종양학과 희귀질병에 초점을 맞추는 글로벌 바이오 제약회사인 EUSA 파마(EUSA Pharma)가 파파 지오바니 23 병원(Papa Giovanni XXIII Hospital) 후원하에 실툭시맙(siltuximab) 시험에 착수했다고 18일 발표했다.  실툭시맙은 인터루킨 6(IL-6)를 공격하는 단클론 항체로서 코로나19 환자 중 심각한 호흡기 합병증을 일으킨 환자들의 치료에 시험적으로 사용될 예정(SISCO ...]]></description><pubDate>Thu, 19 Mar 2020 11:48:57 +0900</pubDate></item><item><title><![CDATA[EUSA Pharma and the Papa Giovanni XXIII Hospital, Bergamo, Italy Announce Initiation of an Observational Case-control Study of Siltuximab in Patients with COVID-19 who have Developed Serious Respiratory Complications]]></title><link>https://www.newswire.co.kr/newsRead.php?no=902707</link><description><![CDATA[HEMEL HEMPSTEAD, England & BERGAMO, Italy--(Business Wire/Korea Newswire)--EUSA Pharma, a global biopharmaceutical company focused on oncology and rare disease, today announced the initiation of the Papa Giovanni XXIII Hospital sponsored study of siltuximab, an interleukin (IL)-6 targeted monoclonal antibody, for the treatment of patients with COVID-19 who have developed serious respiratory complications (Siltuximab In...]]></description><pubDate>Thu, 19 Mar 2020 11:40:52 +0900</pubDate></item><item><title><![CDATA[New ESMO Guidelines Include FOTIVDA®▼(tivozanib) Recommendation for Patients with Advanced Renal Cell Carcinoma]]></title><link>https://www.newswire.co.kr/newsRead.php?no=884666</link><description><![CDATA[HEMEL HEMPSTEAD, England--(Business Wire/Korea Newswire)--HEMEL HEMPSTEAD, England--(BUSINESS WIRE)-- EUSA Pharma (EUSA) welcomes the news that FOTIVDA®▼ (tivozanib) has been included in the new European Society of Medical Oncology (ESMO) clinical practice guidelines for renal cell carcinoma (RCC), published on 21st February 2019.[1]  In the new guidelines tivozanib is included as a first-line treatmen...]]></description><pubDate>Mon, 11 Mar 2019 10:10:00 +0900</pubDate></item><item><title><![CDATA[Outline of New ESMO Guidelines Indicates Inclusion of FOTIVDA®▼ (Tivozanib) for Patients with Advanced Renal Cell Carcinoma]]></title><link>https://www.newswire.co.kr/newsRead.php?no=877522</link><description><![CDATA[HEMEL HEMPSTEAD, England--(Business Wire/Korea Newswire)--EUSA Pharma (EUSA) welcomes the news that FOTIVDA®▼ (tivozanib) is expected to be included in the upcoming European Society of Medical Oncology (ESMO) clinical practice guidelines for advanced renal cell carcinoma (aRCC), anticipated to be published at the end of this year.[1]  The outline of the new proposed guidelines was presented on 19th Oct...]]></description><pubDate>Mon, 22 Oct 2018 18:00:00 +0900</pubDate></item><item><title><![CDATA[EUSA Pharma: NICE Approves the Targeted Cancer Immunotherapy, QARZIBA®▼ (dinutuximab beta) to Treat Children with High-Risk Neuroblastoma]]></title><link>https://www.newswire.co.kr/newsRead.php?no=872329</link><description><![CDATA[HEMEL HEMPSTEAD, England--(Business Wire/Korea Newswire)--EUSA Pharma today welcomed a decision by the National Institute for Health and Care Excellence (NICE) to recommend the use of the targeted cancer immunotherapy, QARZIBA® (dinutuximab beta) to treat children with high-risk neuroblastoma within the NHS in England and Wales.i High-risk neuroblastoma is an aggressive form of neuroblastoma - the most...]]></description><pubDate>Thu, 12 Jul 2018 16:15:00 +0900</pubDate></item><item><title><![CDATA[EUSA 파마: NICE, 고위험군 신경모세포종 어린이 환자 치료에 표적 암 면역치료제 QARZIBA®▼ 승인]]></title><link>https://www.newswire.co.kr/newsRead.php?no=872330</link><description><![CDATA[헤멜 헴스테드, 영국--(Business Wire/뉴스와이어)--EUSA 파마(EUSA Pharma)가 국립보건임상연구소(National Institute for Health and Care Excellence, 이하 NICE) 잉글랜드 및 웨일스의 NHS(영국국가보건서비스) 병원에서 고위험군 신경모세포종(High-risk neuroblastoma) 어린이 환자들을 치료하는 데 표적 암 면역치료제인 QARZIBA®(dinutuximab beta) 사용을 권고하는 결정을 11일 환영했다.i   고위험군 신경모세포종은...]]></description><pubDate>Thu, 12 Jul 2018 16:15:00 +0900</pubDate></item></channel></rss>