<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"><channel><title><![CDATA[Otsuka Pharmaceutical Co., Ltd. 보도자료 - 뉴스와이어]]></title><link>https://www.newswire.co.kr/?md=A10&amp;act=article&amp;no=21001></link><description><![CDATA[Otsuka Pharmaceutical Co., Ltd. 보도자료 - 뉴스와이어 RSS 서비스]]></description><lastBuildDate>Thu, 14 May 2026 02:44:29 +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/2013/11/12_1218276940_20131126090822_1067929226.jpg]]></url></image><language>ko-KR</language><item><title><![CDATA[Efficacy Results of Otsuka’s Delamanid (Deltyba™) for Extensively Drug-Resistant Tuberculosis (XDR-TB) Published in the New England Journal of Medicine]]></title><link>https://www.newswire.co.kr/newsRead.php?no=798000</link><description><![CDATA[TOKYO--(Business Wire/Korea Newswire)--Otsuka Pharmaceutical Co., Ltd. (Otsuka) today announced that data from a post-hoc subset analysis of its Phase IIb clinical trial suggesting potential efficacy of delamanid for the treatment of extensively drug-resistant tuberculosis (XDR-TB) was reported in this week’s New England Journal of Medicine. The analysis found that patients receiving...]]></description><pubDate>Fri, 17 Jul 2015 10:20:00 +0900</pubDate></item><item><title><![CDATA[뉴잉글랜드 의학 저널에 게재된 광범위 내성 결핵(XDR-TB)에 대한 오츠카제약(Otsuka)의 델라마니드(Deltyba®) 효능 결과]]></title><link>https://www.newswire.co.kr/newsRead.php?no=798003</link><description><![CDATA[도쿄--(Business Wire/뉴스와이어)--오츠카 제약(Otsuka)은 광범위 내성 결핵(XDR-TB)에 대한 델라마니드의 효능을 강조하는 2b상 임상 시험에 근거한 사후 하위 분석 데이터가 금주 판 뉴잉글랜드 의학 저널(New England Journal of Medicine)에 보고되었다고 오늘 발표했다. 이 분석에 의하면, 세계보건기구(WHO)에서 권장하는 최적화된 기저 요법(OBR)과 병용하여 델라마니드를 투여한 환자의 경우, 더 이상...]]></description><pubDate>Fri, 17 Jul 2015 10:20:00 +0900</pubDate></item><item><title><![CDATA[Otsuka Pharmaceutical to Acquire Avanir Pharmaceuticals]]></title><link>https://www.newswire.co.kr/newsRead.php?no=776317</link><description><![CDATA[TOKYO--(Business Wire/Korea Newswire)--Otsuka Pharmaceutical Co., Ltd. is pleased to announce an agreement with Avanir Pharmaceuticals, Inc. (“Avanir”) in which Otsuka America, Inc., a US subsidiary, acquires Avanir for USD 3.5 billion in an all-cash tender offer. The contract was signed on December 2, Japan time.  Avanir Pharmaceuticals  Avanir is a biopharmaceutical company special...]]></description><pubDate>Fri, 05 Dec 2014 16:40:00 +0900</pubDate></item><item><title><![CDATA[오츠카제약, 아바니어 파마슈티컬스 인수키로]]></title><link>https://www.newswire.co.kr/newsRead.php?no=776320</link><description><![CDATA[도쿄--(Business Wire/뉴스와이어)--오츠카제약(Otsuka Pharmaceutical Co., Ltd.)은 미국 계열사인 오츠카아메리카(Otsuka America, Inc.)가 아바니어 파마슈티컬스(Avanir Pharmaceuticals, Inc., 이하 아바니어) 주식을 총 35억 달러에 전액 현금으로 공개 매수하기로 아바니어와 합의했다고 발표했다. 이 협약은 12월 2일(일본 시간) 체결됐다.  아바니어 파마슈티컬스(Avanir Pharmaceuticals)  아바니어(...]]></description><image><url><![CDATA[https://file.newswire.co.kr/data/datafile2/thumb/2014/12/20141205163635_2100146848.jpg]]></url></image><pubDate>Fri, 05 Dec 2014 16:40:00 +0900</pubDate></item><item><title><![CDATA[Otsuka Wins European Marketing Authorization for Deltyba™ (delamanid)]]></title><link>https://www.newswire.co.kr/newsRead.php?no=749224</link><description><![CDATA[TOKYO--(Business Wire/Korea Newswire)--Otsuka Pharmaceutical Co., Ltd. (Otsuka) today announced that the European Commission has granted a marketing authorization for Deltyba™ (delamanid) for use as part of an appropriate combination regimen for pulmonary multidrug-resistant tuberculosis (MDR-TB) in adult patients when an effective treatment regimen cannot otherwise be composed for r...]]></description><image><url><![CDATA[https://file.newswire.co.kr/data/datafile2/thumb/2014/05/20140507174047_2047257663.jpg]]></url></image><pubDate>Wed, 07 May 2014 18:05:00 +0900</pubDate></item><item><title><![CDATA[오츠카제약의 신약 델티바(Deltyba®, 델라마니드), 유럽 시장 판매 승인 획득]]></title><link>https://www.newswire.co.kr/newsRead.php?no=749225</link><description><![CDATA[도쿄--(Business Wire/뉴스와이어)--오츠카제약(Otsuka Pharmaceutical Co., Ltd.)이 새로 개발한 델티바(델라마니드[Deltyba™, delamanid])가 내성이나 내약성으로 인해 유효한 치료요법이 구성되지 않는 성인 다제내성 결핵(MDR-TB) 환자를 치료할 수 있는 병용요법의 하나로 유럽위원회(EC)로부터 판매 승인을 받았다.[3]  델티바는 결핵균 (Mycobacterium tuberculosis, MTB) 세포벽의 신진대사를 억제하는...]]></description><image><url><![CDATA[https://file.newswire.co.kr/data/datafile2/thumb/2014/05/20140507175111_3576604742.jpg]]></url></image><pubDate>Wed, 07 May 2014 18:05:00 +0900</pubDate></item><item><title><![CDATA[Otsuka Pharmaceutical‘s Samsca® Approved in Japan as the World’s First Drug Therapy for ADPKD, a Rare Kidney Disease]]></title><link>https://www.newswire.co.kr/newsRead.php?no=743413</link><description><![CDATA[TOKYO--(Business Wire/Korea Newswire)--Otsuka Pharmaceutical Co., Ltd. (Otsuka) today announced it has become the first company in the world to obtain regulatory approval for a pharmacological treatment of autosomal dominant polycystic kidney disease (ADPKD).   Samsca® (generic name: tolvaptan) has been approved in Japan in 7.5-mg and 15-mg tablet forms for extended use for the addit...]]></description><pubDate>Tue, 25 Mar 2014 17:00:00 +0900</pubDate></item><item><title><![CDATA[오츠카제약 ‘삼스카’(Samsca®), 일본에서 희귀 신장 질환 ADPKD의 세계 첫 치료제로 승인]]></title><link>https://www.newswire.co.kr/newsRead.php?no=743414</link><description><![CDATA[도쿄--(Business Wire/뉴스와이어)--오츠카제약주식회사(Otsuka Pharmaceutical Co., Ltd., 이하 오츠카)는 세계 제약 업계 최초로 상염색체우성 다낭성신종(ADPKD)의 약물 치료에 대한 규제 당국의 승인을 획득했다고 오늘 발표했다.   ‘삼스카’(Samsca®)(성분명: 톨밥탄)는 일본에서 7.5mg 및 15mg정의 2가지 제형으로 ADPKD 적응증 추가에 대한 확장 사용을 승인 받았다. 신제형인 삼스카정 30mg도 ADPKD 적...]]></description><pubDate>Tue, 25 Mar 2014 17:00:00 +0900</pubDate></item><item><title><![CDATA[CHMP Recommends Otsuka&#039;s Deltyba™ (delamanid) for EU Approval for Treatment of Multidrug-Resistant Tuberculosis (MDR-TB) in Combination with Optimized Background Regimen (OBR)]]></title><link>https://www.newswire.co.kr/newsRead.php?no=724986</link><description><![CDATA[TOKYO--(Business Wire/Korea Newswire)--Otsuka Pharmaceutical Co., Ltd. (Otsuka) today announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency has recommended approval of DeltybaTM (delamanid) in combination with a WHO recommended optimized background regimen (OBR)1 for the treatment of pulmonary multidrug-resistant tuberculosis (MDR-T...]]></description><pubDate>Tue, 26 Nov 2013 09:00:00 +0900</pubDate></item></channel></rss>