<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"><channel><title><![CDATA[셀트리온헬스케어 보도자료 - 뉴스와이어]]></title><link>https://www.newswire.co.kr/?md=A10&amp;act=article&amp;no=36825></link><description><![CDATA[셀트리온헬스케어 보도자료 - 뉴스와이어 RSS 서비스]]></description><lastBuildDate>Sat, 18 Apr 2026 09:00:15 +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/2024/03/12_1028147215_20240329100700_3636662148.png]]></url></image><language>ko-KR</language><item><title><![CDATA[Celltrion announces positive results for its cocktail therapy candidates including neutralisation data against Omicron variant]]></title><link>https://www.newswire.co.kr/newsRead.php?no=937560</link><description><![CDATA[INCHEON, South Korea--(Business Wire/Korea Newswire)--Celltrion Group announced today results for its cocktail therapy candidates including neutralisation data against the Omicron variant (B.1.1.529).  The Phase I clinical trial is a randomised, double- blind and placebo- controlled trial designed to evaluate the safety, tolerability and pharmacokinetics of CT-P63 in 24 healthy subjects in Poland.[...]]></description><pubDate>Tue, 04 Jan 2022 09:55:56 +0900</pubDate></item><item><title><![CDATA[Celltrion’s COVID-19 Treatment Candidate Receives Korean MFDS Conditional Marketing Authorisation]]></title><link>https://www.newswire.co.kr/newsRead.php?no=918321</link><description><![CDATA[INCHEON, Korea--(Business Wire/Korea Newswire)--Celltrion Group today announced that the Korean Ministry of Food and Drug Safety (MFDS) granted a Conditional Marketing Authorisation (CMA) for the emergency use of Regdanvimab (CT-P59), an anti-COVID-19 monoclonal antibody treatment candidate. The CMA allows for emergency use of CT-P59 in adult patients aged 60 years and over, or with at least ...]]></description><pubDate>Mon, 08 Feb 2021 09:54:59 +0900</pubDate></item><item><title><![CDATA[Celltrion Group announces positive top-line efficacy and safety data from global Phase II/III clinical trial of COVID-19 treatment candidate CT-P59]]></title><link>https://www.newswire.co.kr/newsRead.php?no=917256</link><description><![CDATA[INCHEON, South Korea--(Business Wire/Korea Newswire)--Celltrion Group today announced top-line results from its randomised, double-blind, and placebo controlled global Phase II/III clinical trial of CT-P59, an anti-COVID-19 monoclonal antibody treatment candidate. The Part I of the trial enrolled 327 patients with mild-to-moderate symptoms of COVID-19 across three treatment groups (40mg/kg, 80mg/kg...]]></description><pubDate>Thu, 14 Jan 2021 11:08:06 +0900</pubDate></item></channel></rss>