<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"><channel><title><![CDATA[Janssen 보도자료 - 뉴스와이어]]></title><link>https://www.newswire.co.kr/?md=A10&amp;act=article&amp;no=29201></link><description><![CDATA[Janssen 보도자료 - 뉴스와이어 RSS 서비스]]></description><lastBuildDate>Sat, 25 Apr 2026 19:18:35 +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/2018/03/12_3698601005_20180326112246_1900817475.jpg]]></url></image><language>ko-KR</language><item><title><![CDATA[Janssen Presents Positive Long-Term Efficacy and Safety of SYMTUZA®▼ (D/C/F/TAF) in Treatment-Naïve Adults with HIV-1]]></title><link>https://www.newswire.co.kr/newsRead.php?no=878126</link><description><![CDATA[GLASGOW, Scotland--(Business Wire/Korea Newswire)--The Janssen Pharmaceutical Companies of Johnson &amp; Johnson today unveiled 96-week results from the pivotal Phase 3 AMBER study of SYMTUZA® (darunavir 800 mg, cobicistat 150 mg, emtricitabine 200 mg and tenofovir alafenamide 10 mg (D/C/F/TAF)) at HIV Glasgow in Scotland. D/C/F/TAF is a once-daily darunavir-based single-tablet regimen (STR), fo...]]></description><pubDate>Wed, 31 Oct 2018 11:35:00 +0900</pubDate></item><item><title><![CDATA[Janssen Announces European Commission Approval of JULUCA®▼ (dolutegravir/rilpivirine), the First Two-Drug Regimen, Once-Daily, Single-Pill for the Treatment of HIV-1]]></title><link>https://www.newswire.co.kr/newsRead.php?no=869683</link><description><![CDATA[CORK, Ireland--(Business Wire/Korea Newswire)--The Janssen Pharmaceutical Companies of Johnson &amp; Johnson today announced that the European Commission has granted marketing authorisation for JULUCA® (dolutegravir 50mg [ViiV Healthcare]/rilpivirine 25mg [Janssen Sciences Ireland UC]).[1] ViiV Healthcare, as the marketing authorisation holder, will market dolutegravir/rilpivirine in all cou...]]></description><pubDate>Wed, 23 May 2018 19:20:00 +0900</pubDate></item><item><title><![CDATA[Janssen Announces Positive CHMP Opinion for JULUCA™▼ (dolutegravir/rilpivirine)]]></title><link>https://www.newswire.co.kr/newsRead.php?no=866513</link><description><![CDATA[CORK, Ireland--(Business Wire/Korea Newswire)--The Janssen Pharmaceutical Companies of Johnson &amp; Johnson today announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has issued a Positive Opinion recommending marketing authorisation for JULUCA™ (dolutegravir 50mg [ViiV Healthcare UK Ltd]/rilpivirine 25mg [Janssen Sciences Ireland U...]]></description><pubDate>Mon, 26 Mar 2018 11:30:00 +0900</pubDate></item><item><title><![CDATA[Janssen’s New Darunavir-Based Single Tablet Regimen SYMTUZA® Shows Positive Outcome in Treatment of Antiretroviral-Naïve HIV Patients]]></title><link>https://www.newswire.co.kr/newsRead.php?no=858537</link><description><![CDATA[MILAN--(Business Wire/Korea Newswire)--Janssen’s new once-daily, single tablet combination therapy SYMTUZA® (darunavir/cobicistat/emtricitabine/tenofovir alafenamide [D/C/F/TAF]) has shown to be both highly effective and well-tolerated in treating antiretroviral-naïve HIV-1 patients through 48 weeks in the pivotal phase 3 AMBER study.[1] The results of this study will be presented on...]]></description><pubDate>Thu, 26 Oct 2017 09:15:00 +0900</pubDate></item><item><title><![CDATA[Janssen Receives Positive CHMP Opinion for SYMTUZA™ The First Darunavir-Based Single-Tablet Regimen for the Treatment of HIV]]></title><link>https://www.newswire.co.kr/newsRead.php?no=853801</link><description><![CDATA[BEERSE, Belgium--(Business Wire/Korea Newswire)--Janssen-Cilag International NV (Janssen) today announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has issued a Positive Opinion recommending marketing authorisation for SYMTUZA™ (darunavir/cobicistat/emtricitabine/tenofovir alafenamide [D/C/F/TAF]), a once-daily darunavir-based single ...]]></description><pubDate>Fri, 28 Jul 2017 09:40:00 +0900</pubDate></item><item><title><![CDATA[얀센 ‘심투자’, CHMP ‘긍정 의견’ 받아… HIV 치료를 위한 최초의 다루나비르 기반 단일복합정]]></title><link>https://www.newswire.co.kr/newsRead.php?no=853802</link><description><![CDATA[비어스, 벨기에--(Business Wire/뉴스와이어)--얀센-실락 인터내셔널(Janssen-Clog International NV, 이하 얀센)이 유럽의약품청(European Medicines Agency, 약칭 EMA) 산하 약물사용자문위원회(Committee for Medicinal Products for Human Use, 약칭 CHMP)가 ‘심투자’(SYMTUZA™:  다루나비르(darunavir)/코비시스타트(cobicistat)/엠트리시타빈(emtricitabine)/테노포비르 알라페나미드(tenofovir alafenamide), 약칭...]]></description><pubDate>Fri, 28 Jul 2017 09:40:00 +0900</pubDate></item><item><title><![CDATA[Janssen Announces Phase 3 Pivotal Study Results for Darunavir-Based Complete Treatment Regimen]]></title><link>https://www.newswire.co.kr/newsRead.php?no=853698</link><description><![CDATA[PARIS--(Business Wire/뉴스와이어)--Janssen-Cilag International NV (Janssen) today announced that an investigational single-tablet regimen (STR) containing darunavir is effective and well tolerated. Results from the pivotal Phase 3 EMERALD study showed that a once-daily STR containing darunavir 800 mg, cobicistat 150 mg, emtricitabine 200 mg and tenofovir alafenamide 10 mg [D/C/F/...]]></description><pubDate>Wed, 26 Jul 2017 13:50:00 +0900</pubDate></item><item><title><![CDATA[Data Published in The Lancet Shows High Efficacy at 96 Weeks for First Investigational Two-Drug, Long-Acting Injectable HIV Regimen]]></title><link>https://www.newswire.co.kr/newsRead.php?no=853586</link><description><![CDATA[CORK, Ireland--(Business Wire/Korea Newswire)--Janssen Sciences Ireland UC, one of the Janssen Pharmaceutical Companies of Johnson &amp; Johnson (Janssen) today announced that a regimen of two investigational long-acting, injectable formulations of HIV medicines —Janssen’s rilpivirine and ViiV Healthcare’s cabotegravir — given together every 4 or 8 weeks was as effective as 3-drug oral antir...]]></description><pubDate>Mon, 24 Jul 2017 18:10:00 +0900</pubDate></item><item><title><![CDATA[Pimodivir Alone or in Combination with Oseltamivir Demonstrated a Significant Reduction in Viral Load in Adults with Influenza A]]></title><link>https://www.newswire.co.kr/newsRead.php?no=851583</link><description><![CDATA[SHANGHAI--(Business Wire/Korea Newswire)--Janssen Pharmaceuticals, Inc. (Janssen) today announced results from the Phase 2b Topaz Trial which demonstrated that treatment with pimodivir (JNJ-63623872) significantly decreased viral load over seven days versus placebo, in adult patients with acute, uncomplicated seasonal influenza A. Patients treated with pimodivir and oseltamivir (OST) al...]]></description><pubDate>Thu, 15 Jun 2017 11:15:00 +0900</pubDate></item></channel></rss>