<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"><channel><title><![CDATA[LEO Pharma A/S 보도자료 - 뉴스와이어]]></title><link>https://www.newswire.co.kr/?md=A10&amp;act=article&amp;no=37552></link><description><![CDATA[LEO Pharma A/S 보도자료 - 뉴스와이어 RSS 서비스]]></description><lastBuildDate>Tue, 07 Apr 2026 05:42:06 +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/2021/04/12_3554238800_20210426085749_2064904606.jpg]]></url></image><language>ko-KR</language><item><title><![CDATA[LEO Pharma Announces FDA Approval of ANZUPGO® (delgocitinib) Cream in the U.S.]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1015599</link><description><![CDATA[BALLERUP, Denmark--(Business Wire/Korea Newswire)--LEO Pharma, a global leader in medical dermatology, announced today that the U.S. Food and Drug Administration (FDA) has approved ANZUPGO® (delgocitinib) cream (20 mg/g) for the topical treatment of moderate-to-severe chronic hand eczema (CHE) in adults who have had an inadequate response to, or for whom topical corticosteroids are not advisable...]]></description><pubDate>Fri, 25 Jul 2025 11:30:00 +0900</pubDate></item><item><title><![CDATA[레오 파마 ‘ANZUPGO®’ 크림, 미국 FDA 승인 획득]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1015600</link><description><![CDATA[발레룹, 덴마크--(Business Wire/뉴스와이어)--의료 피부과 분야의 글로벌 리더인 레오 파마(LEO Pharma)는 미국 식품의약국(FDA)이 ‘안줍고(ANZUPGO®, 성분명 델고시티닙(delgocitinib))’ 크림(20mg/g)을 국소 코르티코스테로이드에 반응이 불충분하거나 사용이 권장되지 않는 중등도에서 중증의 만성 손 습진(CHE) 성인 환자의 국소 치료제로 승인했다고 발표했다.[1]  안줍고는 CHE를 앓는 성인 환자를 위한 혁신적인 ...]]></description><pubDate>Fri, 25 Jul 2025 11:30:00 +0900</pubDate></item><item><title><![CDATA[LEO Pharma Announces European Commission Approval of Adtralza® (tralokinumab) for the Treatment of Moderate-to-Severe Atopic Dermatitis in Adolescents]]></title><link>https://www.newswire.co.kr/newsRead.php?no=953923</link><description><![CDATA[Ballerup, Denmark--(Business Wire/Korea Newswire)--NOT FOR DISTRIBUTION IN THE UK OR IRELAND  LEO Pharma A/S, a global leader in medical dermatology, today announced that the European Commission (EC) has extended the marketing authorization for Adtralza® (tralokinumab) to include adolescents aged 12 to 17 with moderate-to-severe atopic dermatitis (AD) who are candidates for systemic therapy.  “S...]]></description><pubDate>Fri, 21 Oct 2022 11:10:00 +0900</pubDate></item><item><title><![CDATA[레오파마의 애드트랄자, EU가 중증도-중증 청소년 아토피 피부염 환자에 사용 승인]]></title><link>https://www.newswire.co.kr/newsRead.php?no=953924</link><description><![CDATA[발러럽, 덴마크--(Business Wire/뉴스와이어)--영국이나 아일랜드서 배포 불가  피부의학 분야의 세계 선도 기업인 레오파마(LEO Pharma A/S)는 유럽연합(EU) 집행위원회(EC)가 애드트랄자(dtralza®)(성분명: 트랄로키누맙(tralokinumab)의 판매 허가를 전신 요법 대상자인 12~17세의 중등도-중증 청소년 아토피 피부염(AD) 환자까지 포함한다고 발표했다.  ECZTRA 6 임상시험 대표 연구자인 독일 뮌헨 루트비히 막시밀리...]]></description><pubDate>Fri, 21 Oct 2022 11:10:00 +0900</pubDate></item><item><title><![CDATA[LEO Pharma Receives Positive CHMP Opinion of Adtralza® (tralokinumab) for the Treatment of Adolescents With Moderate-to-Severe Atopic Dermatitis]]></title><link>https://www.newswire.co.kr/newsRead.php?no=951528</link><description><![CDATA[Ballerup, Denmark--(Business Wire/Korea Newswire)--LEO Pharma A/S, a global leader in medical dermatology, today announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has adopted a positive opinion recommending to extend the approval of Adtralza® (tralokinumab) in the European Union (EU) to include adolescents aged 12 to 17 with moderate-...]]></description><pubDate>Mon, 19 Sep 2022 14:10:00 +0900</pubDate></item><item><title><![CDATA[레오파마의 애드트랄자, 유럽서 중등도 이상의 청소년 AD 환자 치료제로 허가 권고]]></title><link>https://www.newswire.co.kr/newsRead.php?no=951529</link><description><![CDATA[발러럽, 덴마크--(Business Wire/뉴스와이어)--유럽의약청(EMA)의 약물사용자문위원회(CHMP)가 애드트랄자(Adtralza®)(성분명 트랄로키누맙[tralokinumab])의 유럽연합(EU) 사용 연령대를 전신 요법 후보군인 중등도 이상의 아토피성 피부염(AD) 청소년(12~17세)으로 확대하는 내용을 권고하는 긍정적인 의견을 채택했다고 피부과학 분야의 글로벌 선도기업인 레오파마(LEO Pharma A/S)가 16일 발표했다.   CHMP가 권고한...]]></description><pubDate>Mon, 19 Sep 2022 14:10:00 +0900</pubDate></item><item><title><![CDATA[LEO Pharma Announces FDA Approval of Adbry™ (tralokinumab) as the First and Only Treatment Specifically Targeting IL-13 for Adults With Moderate-to-Severe Atopic Dermatitis]]></title><link>https://www.newswire.co.kr/newsRead.php?no=937476</link><description><![CDATA[Ballerup, Denmark--(Business Wire/Korea Newswire)--LEO Pharma A/S, a global leader in medical dermatology, announced today that the U.S. Food and Drug Administration (FDA) has approved Adbry™ (tralokinumab) for the treatment of moderate-to-severe atopic dermatitis in adults 18 years or older whose disease is not adequately controlled with topical prescription therapies or when those therapies ar...]]></description><pubDate>Fri, 31 Dec 2021 14:10:00 +0900</pubDate></item><item><title><![CDATA[레오파마, 중증도-중증 성인 아토피 피부염 환자 위한 최초의 IL-13 표적 치료제 애드브리(트랄로키누맙) FDA 승인]]></title><link>https://www.newswire.co.kr/newsRead.php?no=937477</link><description><![CDATA[발러럽, 덴마크--(Business Wire/뉴스와이어)--피부과학 분야의 글로벌 선도기업인 레오파마(LEO Pharma A/S)는 자사의 성인 아토피 피부염 치료제인 애드브리(Adbry™)가 미국 식품의약국(FDA)의 승인을 받았다고 28일 발표했다.  애드브리는 국소 치료제로 적절히 조절되지 않거나 이러한 치료제가 권장되지 않는 중증도-중증 아토피 피부염을 가진 18세 이상 성인 환자를 대상으로 한 치료제로, 국소 코르티코스테로이...]]></description><pubDate>Fri, 31 Dec 2021 14:10:00 +0900</pubDate></item><item><title><![CDATA[LEO Pharma Presents Long-Term Safety and Efficacy Data for Tralokinumab in Adults With Moderate-to-Severe Atopic Dermatitis at AAD VMX 2021]]></title><link>https://www.newswire.co.kr/newsRead.php?no=922213</link><description><![CDATA[BALLERUP, Denmark, & MADISON, N.J.--(Business Wire/Korea Newswire)--LEO Pharma A/S, a global leader in medical dermatology, today announced results on the long-term safety and efficacy profile of tralokinumab in adult patients with moderate-to-severe atopic dermatitis. Results were shared as an oral presentation during the American Academy of Dermatology Virtual Meeting Experience (AAD VMX) 2021.  Tralokinumab i...]]></description><pubDate>Mon, 26 Apr 2021 10:10:00 +0900</pubDate></item><item><title><![CDATA[LEO Pharma Receives Positive CHMP Opinion of Adtralza® (tralokinumab) for the Treatment of Adults With Moderate-to-Severe Atopic Dermatitis]]></title><link>https://www.newswire.co.kr/newsRead.php?no=922208</link><description><![CDATA[BALLERUP, Denmark--(Business Wire/Korea Newswire)--LEO Pharma A/S, a global leader in medical dermatology, today announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has adopted a positive opinion and recommended granting a marketing authorization of Adtralza® (tralokinumab) for the treatment of moderate-to-severe atopic dermatitis in ad...]]></description><pubDate>Mon, 26 Apr 2021 09:20:00 +0900</pubDate></item></channel></rss>