Resolution Therapeutics Announces Approval of Clinical Trial Application by AEMPS to Expand Phase 1/2 EMERALD Study of RTX001 Into Spain
Resolution Therapeutics Announces Approval of Clinical Trial Application by AEMPS to Expand Phase 1/2 EMERALD Study of RTX001 Into Spain
- EMERALD Study will investigate the safety and efficacy of RTX001, an engineered macrophage cell therapy, in patients with end-stage liver disease
- emerald研究將調查RTX001這一工程化巨噬細胞治療在晚期肝病患者中的安全性和有效性
- Recruitment already underway in the U.K., following recent MHRA approval
- 在獲得最近MHRA批准後,招募工作已在英國展開
EDINBURGH, Scotland and LONDON, Nov. 19, 2024 /PRNewswire/ -- Resolution Therapeutics Limited ("Resolution"), a clinical-stage biopharmaceutical company pioneering regenerative macrophage therapies in inflammatory and fibrotic diseases, today announces it has received approval of a clinical trial application from the Spanish Agency of Medicines and Medical Products (AEMPS) to commence the Phase 1/2 EMERALD Study evaluating its lead candidate RTX001 in Spain.
蘇格蘭愛丁堡和倫敦,2024年11月19日 / PRNewswire / -- Resolution Therapeutics Limited("Resolution")是一家臨床階段生物製藥公司,致力於在炎症和纖維化疾病中開創再生巨噬細胞療法,今天宣佈已獲得西班牙藥品和醫療產品管理局(AEMPS)批准,開始在西班牙進行首個階段1/2 emerald研究,評估其主導候選者RTX001。
EMERALD is an open-label, first-in-human Phase 1/2 study which will investigate the safety and efficacy of RTX001 in patients with end-stage liver disease. The primary analysis will focus on safety and major clinical events, including death. The study will also evaluate biomarkers, such as the Model for End-Stage Liver Disease (MELD) score, which is used to assess disease severity and prioritise patients for a liver transplant.
emerald是一個開放標籤、首次在人類中進行的階段1/2研究,將調查RTX001在晚期肝病患者中的安全性和有效性。主要分析將側重於安全性和重大臨床事件,包括死亡。該研究還將評估生物標誌物,如用於評估疾病嚴重程度和優先考慮肝移植患者的晚期肝病模型(MELD)評分。
The EMERALD study received its first clinical trial authorisation from the U.K. Medicines and Healthcare products Regulatory Agency (MHRA) earlier this year, and started recruiting patients in October 2024 in the U.K. It is expected to start recruiting patients in Spain in the second quarter of 2025.
emerald研究早在今年年初獲得了英國藥品和醫療保健產品監管局(MHRA)的首次臨床試驗授權,並於2024年10月在英國開始招募患者。預計將在2025年第二季度在西班牙開始招募患者。
Dr Clifford Brass, Chief Medical Officer of Resolution Therapeutics, commented: "We are excited to have received approval from the AEMPS to expand our Phase 1/2 EMERALD study for RTX001 into Spain. This builds on the existing clinical trial authorisation in the U.K, where patient recruitment is under way, and further demonstrates the momentum Resolution looks to carry into 2025, as we deliver on our mission of developing macrophage therapies to transform the outcomes of patients with inflammatory and fibrotic diseases."
Resolution Therapeutics的首席醫療官Clifford Brass博士評論道:"我們很高興獲得AEMPS的批准,將我們的階段1/2 emerald研究擴展至西班牙。這建立在英國已有的臨床試驗授權之上,目前患者招募正在進行中,進一步展示了Resolution希望在2025年繼續保持的勢頭,我們致力於開發巨噬細胞療法,以改變炎症和纖維化疾病患者的治療結果。"
The AEMPS approval follows the presentation of preclinical data on RTX001 at the American Association for the Study of Liver Disease (AASLD) The Liver Meeting 2024, held in San Diego from 15-19 November 2024, demonstrating the superior anti-fibrotic and anti-inflammatory effect of IL-10-MMP9 engineered macrophages over non-engineered macrophages. Together, these data underscore the potential of engineered macrophages to address high unmet medical needs in end-stage liver disease.
AEMPS的批准是在2024年11月15日至19日於聖地亞哥舉行的美國肝病研究協會(AASLD)肝臟會議2024上對RTX001的臨床前數據進行展示後獲得的,顯示IL-10-MMP9工程化巨噬細胞相較於非工程化巨噬細胞具有更優越的抗纖維化和抗炎症效果。這些數據共同強調了工程化巨噬細胞在解決晚期肝病中尚未滿足的醫療需求方面的潛力。
About RTX001
關於RTX001
RTX001 is an engineered, autologous regenerative macrophage therapy with enhanced anti-fibrotic and anti-inflammatory effect. The product candidate is engineered with IL-10-MMP9 mRNA to enhance the natural regenerative properties of macrophages for superior efficacy and durability. RTX001 is being evaluated in the ongoing Phase 1/2 EMERALD study.
RTX001是一種工程、自體再生巨噬細胞治療,具有增強的抗纖維化和抗炎效果。該產品候選者通過IL-10-MMP9 mRNA工程化,以增強巨噬細胞的天然再生特性,實現卓越的療效和持久性。RTX001正在進行中的EMERALD第1/2期研究中得到評估。
About EMERALD
關於EMERALD
EMERALD is a first-in-human, open-label Phase 1/2 interventional study assessing the safety and efficacy of RTX001 in patients with end-stage liver disease who have recovered from a recent hepatic decompensation. It is conducted in the UK and Spain and began recruiting patients in October 2024. For more information, please visit .
emerald是一項首次在人類中進行的、開放標籤的1/2期干預研究,旨在評估RTX001在經歷過近期肝功能失代償的末期肝病患者中的安全性和有效性。該研究在英國和西班牙進行,並於2024年10月開始招募患者。如需更多信息,請訪問。
About Resolution Therapeutics
關於Resolution Therapeutics
Resolution Therapeutics is a clinical-stage biopharmaceutical company pioneering regenerative macrophage therapy in inflammatory and fibrotic diseases. The Company leverages its proprietary platform to develop macrophages with pro-regenerative properties for superior patient outcomes. Resolution's initial focus is on developing RTX001, its lead product with first-in-class potential supported by preclinical data demonstrating anti-fibrotic and anti-inflammatory advantages relative to non-engineered macrophages, to treat patients with end-stage liver disease. The Company is also advancing efforts to expand its platform into inflammatory and fibrotic indications beyond liver disease, including graft-vs-host disease (GVHD) and lung fibrosis. Resolution, a spinout from Professor Stuart Forbes's lab at the University of Edinburgh, is based in Edinburgh and London. Learn more by visiting and engage with us on LinkedIn.
Resolution Therapeutics是一家臨床階段的生物製藥公司,致力於在炎症性和纖維化疾病中開創再生巨噬細胞療法。該公司利用其專有平台開發具有促再生特性的巨噬細胞,以實現優越的患者預後。Resolution最初專注於開發RTX001,其主力產品具有首創潛力,並得到臨床前數據的支持,顯示相對於非經過工程處理的巨噬細胞具有抗纖維化和抗炎優勢,用於治療晚期肝病患者。該公司還在推進其努力,將其平台拓展到超出肝病範圍的炎症性和纖維化指徵,包括移植物抗宿主病(GVHD)和肺纖維化。Resolution是從英國愛丁堡大學Stuart Forbes教授實驗室分離出來的,總部設在愛丁堡和倫敦。欲了解更多,請訪問,也歡迎關注我們的LinkedIn。
SOURCE Resolution Therapeutics
來源:Resolution Therapeutics
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