<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"><channel><title><![CDATA[Merck 보도자료 - 뉴스와이어]]></title><link>https://www.newswire.co.kr/?md=A10&amp;act=article&amp;no=48198></link><description><![CDATA[Merck 보도자료 - 뉴스와이어 RSS 서비스]]></description><lastBuildDate>Wed, 29 Apr 2026 18:13:13 +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/2025/06/12_1028147215_20250610133216_7620378639.jpg]]></url></image><language>ko-KR</language><item><title><![CDATA[FDA Accepts New Drug Application for Pimicotinib for the Treatment of Tenosynovial Giant Cell Tumor]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1026821</link><description><![CDATA[DARMSTADT, Germany--(Business Wire/Korea Newswire)--Merck, a leading science and technology company, announced today that the U.S. Food and Drug Administration (FDA) has accepted the company’s new drug application (NDA) for pimicotinib as a systemic treatment for patients with tenosynovial giant cell tumor (TGCT). The application is based on the primary results and longer-term follow-up of the gl...]]></description><pubDate>Tue, 13 Jan 2026 09:02:34 +0900</pubDate></item><item><title><![CDATA[Pimicotinib Approved as Systemic Treatment in China for Tenosynovial Giant Cell Tumor]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1025903</link><description><![CDATA[DARMSTADT, Germany--(Business Wire/Korea Newswire)--Merck, a leading science and technology company, announced today that following Priority Review, the China National Medical Products Administration (NMPA) has approved pimicotinib for the treatment of adult patients with symptomatic tenosynovial giant cell tumor (TGCT) for which surgical resection will potentially cause functional limitation or ...]]></description><pubDate>Tue, 23 Dec 2025 09:19:27 +0900</pubDate></item><item><title><![CDATA[Merck Takes Patient-Directed Approach to Bring Innovation to the Treatment of Rare Neuromuscular Disorder, Generalized Myasthenia Gravis]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1023820</link><description><![CDATA[DARMSTADT, Germany--(Business Wire/Korea Newswire)--Merck, a leading science and technology company, today announced the U.S. Food and Drug Administration (FDA) has granted Fast Track designation for cladribine capsules for the treatment of the rare, chronic autoimmune neuromuscular disorder, generalized Myasthenia Gravis (gMG). In June 2023, the FDA granted Orphan Drug Designation for cladribine...]]></description><pubDate>Tue, 25 Nov 2025 09:40:27 +0900</pubDate></item><item><title><![CDATA[Pimicotinib Treatment Demonstrates Deep and Durable Tumor Responses and Continued Improvements in Pain and Function for Patients with TGCT]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1020898</link><description><![CDATA[DARMSTADT, Germany--(Business Wire/Korea Newswire)--Merck, a leading science and technology company, today announced the presentation of longer-term results from the global Phase 3 MANEUVER trial evaluating pimicotinib, an investigational colony stimulating factor-1 receptor (CSF-1R) inhibitor in development by Abbisko Therapeutics Co., Ltd., for the treatment of patients with tenosynovial giant ...]]></description><pubDate>Sun, 19 Oct 2025 16:02:01 +0900</pubDate></item><item><title><![CDATA[Merck to Present New Data Highlighting Durable Effects of MAVENCLAD® in Relapsing Multiple Sclerosis (RMS) at ECTRIMS 2025]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1019028</link><description><![CDATA[DARMSTADT, Germany--(Business Wire/Korea Newswire)--Not intended for UK-, US- or Canada-based media  Merck, a leading science and technology company, today announced the presentation of over 30 abstracts from its multiple sclerosis (MS) portfolio. New four-year data from two large Phase 4 studies highlight the long-term efficacy, favorable disability outcomes and durable impact of MAVENCLAD® (cla...]]></description><pubDate>Thu, 18 Sep 2025 13:55:00 +0900</pubDate></item><item><title><![CDATA[Merck Presents Results on Efficacy and Safety of Enpatoran in Systemic Lupus Erythematosus (SLE) at EULAR 2025]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1013017</link><description><![CDATA[DARMSTADT, Germany--(Business Wire/Korea Newswire)--Not intended for UK-, US- or Canada-based media  Merck, a leading science and technology company, today announced the presentation of detailed results from Cohort B of the global Phase 2 WILLOW study (NCT05162586 ) evaluating enpatoran, an investigational, oral, novel TLR7/8 inhibitor in systemic lupus erythematosus (SLE). Although it did not me...]]></description><pubDate>Fri, 13 Jun 2025 08:53:06 +0900</pubDate></item><item><title><![CDATA[China’s Center for Drug Evaluation Accepts Merck’s Application for Marketing Authorization of Pimicotinib for Treatment of Tenosynovial Giant Cell Tumor]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1012803</link><description><![CDATA[DARMSTADT, Germany--(Business Wire/Korea Newswire)--Merck, a leading science and technology company, today announced that the Center for Drug Evaluation (CDE) of the China National Medical Products Administration (NMPA) officially accepted the company’s application for marketing authorization of pimicotinib as a Class 1 innovative drug for adult patients with tenosynovial giant cell tumors (TGCT)...]]></description><pubDate>Tue, 10 Jun 2025 14:10:00 +0900</pubDate></item></channel></rss>