HighTide Therapeutics Announces First Patient Dosed in Phase 2b Clinical Study Evaluating HTD1801 in NASH (the CENTRICITY study) ACN Newswire

HighTide Therapeutics Announces First Patient Dosed in Phase 2b Clinical Study Evaluating HTD1801 in NASH (the CENTRICITY study)

ROCKVILLE, MD and SHENZHEN, CHINA, Jan 11, 2023 - (ACN Newswire via SEAPRWire.com) - HighTide Therapeutics Inc. ("HighTide"), a globally integrated clinical-stage biopharmaceutical company developing novel multifunctional therapies for metabolic and digestive diseases, today announced the dosing of the first patient in a Phase 2b clinical study evaluating HTD1801 for the treatment of nonalcoholic steatohepatitis ("NASH").This double-blind, randomized, placebo-controlled, multicentre Phase 2b study will evaluate the effect of HTD1801, 1250 mg twice daily (BID), compared to placebo BID on histologic improvement in adult subjects with NASH and liver fibrosis who also have type 2 diabetes mellitus ("T2DM") or pre-diabetes. The study will enroll approximately 210 subjects with biopsy-confirmed NASH and evidence of stage 2 or stage 3 liver fibrosis. Subjects will receive HTD1801 for up to 60 weeks."Nonalcoholic fatty liver disease ("NAFLD") is the most prevalent chronic liver disease worldwide with a global prevalence of 25.2% to 29.8%. Of those with NAFLD, about 20% have NASH. Patients with NASH and T2DM or prediabetes are at increased risk of progressive liver disease and cardiometabolic complications," said Dr. Liping Liu, founder and Chief Executive Officer of HighTide. "This first patient dosing marks a key milestone for the development of HTD1801 for the treatment of patients with NASH, building on data from our Phase 2a study which showed HTD1801 was associated with meaningful improvements in liver fat, markers of liver Injury and fibrosis as well as cardiometabolic factors (HbA1c, lipids, and weight) after 18 weeks." About NASHNASH, a severe form of nonalcoholic fatty liver disease (NAFLD), is a chronic, complex liver disease characterized by hepatitis - inflammation of the liver - and liver cell damage, which can lead to fibrosis of the liver. NASH can also lead to cirrhosis and liver cancer. NASH patients with T2DM or impaired glucose tolerance are more likely to progress to more severe disease and to develop complications that lead to increased mortality. Prevalence of NASH is on the rise and may soon surpass hepatitis C as a cause for liver transplant in the U.S. and Europe. Currently, there are no approved therapies for NASH.About HighTide TherapeuticsHighTide is a globally integrated clinical-stage biopharmaceutical company focusing on the discovery and development of novel multifunctional therapies for metabolic and digestive diseases with significant unmet medical needs. The company's lead drug candidate, HTD1801, is a first-in-class new molecular entity, currently in clinical development for the treatment of type 2 diabetes (T2DM), nonalcoholic steatohepatitis (NASH), severe hypertriglyceridemia (SHTG), and primary sclerosing cholangitis (PSC). HTD1801 has received Fast Track designation from the U.S. FDA for both NASH and PSC, as well as Orphan Drug designation for PSC. In China, HTD1801 has been included in the National Major New Drug Innovation Program. For more information, please visit www.hightidetx.com.ContactsNadia Gaoir@hightidetx.com Copyright 2023 ACN Newswire. All rights reserved. (via SEAPRWire)
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君圣泰HTD1801治疗非酒精性脂肪性肝炎(NASH)的临床IIb 期研究(CENTRICITY研究)完成首例患者给药 ACN Newswire

君圣泰HTD1801治疗非酒精性脂肪性肝炎(NASH)的临床IIb 期研究(CENTRICITY研究)完成首例患者给药

ROCKVILLE, MD and SHENZHEN, CHINA, Jan 11, 2023 - (亚太商讯 via SEAPRWire.com) - 君圣泰(HighTide Therapeutics Inc.) 宣布,HTD1801治疗非酒精性脂肪性肝炎(NASH)的 临床IIb 期研究完成首例患者给药。本项随机、双盲、安慰剂对照的临床IIb 期多中心研究旨在评估与安慰剂相比,HTD1801对患有 NASH 和肝纤维化且合并 2 型糖尿病(T2DM)或前期糖尿病的受试者的组织学改善程度。本研究将入组约 210 名经活检确诊NASH且肝纤维化处于2 期或 3 期的成年受试者。受试者将接受HTD1801治疗至多 60 周。“非酒精性脂肪性肝病(NAFLD)是全世界最普遍的慢性肝病之一。全球患病率高达25.2%至29.8%。NAFLD 患者中约 20% 患有 NASH。NASH 合并 T2DM 或前期糖尿病将增加肝病恶化和心血管代谢并发症的风险,” 君圣泰创始人、首席执行官刘利平博士说,“本次首例患者给药标志着HTD1801开发NASH适应症的一个重要里程碑。之前完成的IIa 期研究表明,HTD1801给药18周后,肝脂肪、肝损伤和纤维化的标志物以及心血管代谢指标(HbA1c、血脂及体重)均呈现积极改善。这为本次IIb期研究奠定了坚实的基础。”关于非酒精性脂肪性肝炎(NASH)NASH是非酒精性脂肪性肝病(NAFLD)的重症形式,是一种慢性、复杂的肝病。其特征是肝脏炎症和肝细胞损伤,可导致肝脏纤维化、肝硬化和肝癌。合并T2DM或糖耐量受损的NASH患者进展到重症的风险更高,也更可能出现并发症,导致死亡率上升。NASH的患病率正在上升,预计即将超越丙型肝炎成为欧、美肝移植的首要病因。目前,中、美、欧、日等主流医药市场均尚无获批的 NASH 疗法。关于君圣泰(HighTide Therapeutics Inc.)君圣泰是一家全球一体化的临床阶段生物技术公司,专注代谢性疾病、消化系统疾病等领域的重大未满足临床需求。在经验丰富的国际化高管团队和世界一流的科学顾问委员会的领导下,公司立足源头创新,以患者的综合临床获益和整体健康改善为目标,开发“First-in-Class”多靶点原创新药。基于自主知识产权,公司已构建丰富的产品管线,在全球推进多项中、后期临床试验,开发2型糖尿病(T2DM)、非酒精性脂肪性肝炎(NASH)、严重高甘油三酯血症(SHTG)、原发性硬化性胆管炎(PSC)等适应症。作为同类首创的多靶点新分子实体,HTD1801被美国FDA授予2项“快速通道资格认定”、1项“孤儿药资格认定”,并获得国家“十三五”“重大新药创制”科技重大专项支持。欲知更多资讯或沟通潜在合作,敬请访问 https://hightidetx.com 或垂询 pr@hightidetx.com、ir@hightidetx.com。 Copyright 2023 亚太商讯. All rights reserved. (via SEAPRWire)
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