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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

Resolution Therapeutics宣布AEMPS批准临床试验申请,以将RTX001的1/2期emerald研究扩展到西班牙
PR Newswire ·  11/19 03:30

- EMERALD Study will investigate the safety and efficacy of RTX001, an engineered macrophage cell therapy, in patients with end-stage liver disease

- emerald研究将调查RTX001这一工程化巨噬细胞治疗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

- 在获得最近MHRA批准后,招募工作已在英国展开

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.

苏格兰爱丁堡和伦敦,2024年11月19日 / PRNewswire / -- Resolution Therapeutics Limited("Resolution")是一家临床阶段生物制药公司,致力于在炎症和纤维化疾病中开创再生巨噬细胞疗法,今天宣布已获得西班牙药品和医疗产品管理局(AEMPS)批准,开始在西班牙进行首个阶段1/2 emerald研究,评估其主导候选者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是一个开放标签、首次在人类中进行的阶段1/2研究,将调查RTX001在晚期肝病患者中的安全性和有效性。主要分析将侧重于安全性和重大临床事件,包括死亡。该研究还将评估生物标志物,如用于评估疾病严重程度和优先考虑肝移植患者的晚期肝病模型(MELD)评分。

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研究早在今年年初获得了英国药品和医疗保健产品监管局(MHRA)的首次临床试验授权,并于2024年10月在英国开始招募患者。预计将在2025年第二季度在西班牙开始招募患者。

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的首席医疗官Clifford Brass博士评论道:"我们很高兴获得AEMPS的批准,将我们的阶段1/2 emerald研究扩展至西班牙。这建立在英国已有的临床试验授权之上,目前患者招募正在进行中,进一步展示了Resolution希望在2025年继续保持的势头,我们致力于开发巨噬细胞疗法,以改变炎症和纤维化疾病患者的治疗结果。"

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日于圣地亚哥举行的美国肝病研究协会(AASLD)肝脏会议2024上对RTX001的临床前数据进行展示后获得的,显示IL-10-MMP9工程化巨噬细胞相较于非工程化巨噬细胞具有更优越的抗纤维化和抗炎症效果。这些数据共同强调了工程化巨噬细胞在解决晚期肝病中尚未满足的医疗需求方面的潜力。

About RTX001

关于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是一种工程、自体再生巨噬细胞治疗,具有增强的抗纤维化和抗炎效果。该产品候选者通过IL-10-MMP9 mRNA工程化,以增强巨噬细胞的天然再生特性,实现卓越的疗效和持久性。RTX001正在进行中的EMERALD第1/2期研究中得到评估。

About EMERALD

关于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是一项首次在人类中进行的、开放标签的1/2期干预研究,旨在评估RTX001在经历过近期肝功能失代偿的末期肝病患者中的安全性和有效性。该研究在英国和西班牙进行,并于2024年10月开始招募患者。如需更多信息,请访问。

About Resolution Therapeutics

关于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是一家临床阶段的生物制药公司,致力于在炎症性和纤维化疾病中开创再生巨噬细胞疗法。该公司利用其专有平台开发具有促再生特性的巨噬细胞,以实现优越的患者预后。Resolution最初专注于开发RTX001,其主力产品具有首创潜力,并得到临床前数据的支持,显示相对于非经过工程处理的巨噬细胞具有抗纤维化和抗炎优势,用于治疗晚期肝病患者。该公司还在推进其努力,将其平台拓展到超出肝病范围的炎症性和纤维化指征,包括移植物抗宿主病(GVHD)和肺纤维化。Resolution是从英国爱丁堡大学Stuart Forbes教授实验室分离出来的,总部设在爱丁堡和伦敦。欲了解更多,请访问,也欢迎关注我们的LinkedIn。

SOURCE Resolution Therapeutics

来源:Resolution Therapeutics

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