share_log

China Medical System: New Drug Application of Desidustat Tablets Accepted in China

China Medical System: New Drug Application of Desidustat Tablets Accepted in China

中国医疗系统:地舒司他片新药申请在中国受理
GlobeNewswire ·  04/23 09:46

SHENZHEN, CHINA, April 23, 2024 (GLOBE NEWSWIRE) --

中国深圳,2024 年 4 月 23 日(GLOBE NEWSWIRE)—

  • Desidustat Tablets are novel, oral HIF-PHI for treating anaemia in non-dialysis adult chronic kidney disease patients. The Product is administrated orally, thus expecting to improve the treatment compliance of patients and to meet the unmet treatment needs in the field of CKD anaemia, including both dialysis and non-dialysis patients.
  • China Phase III trial of the Product has demonstrated positive results. The primary endpoint has indicated that Desidustat is more effective than placebo in increasing Hb level.
  • Currently, 4 innovative drugs of CMS have entered into commercialization stage. Meanwhile, continuous advance of products' clinical development and registration process such as Desidustat Tablets is expected to enrich the Group's marketed innovative product portfolio, and generate new driving force to the Group's sustainable and healthy development.
  • Desidustat 片剂是一种新型的口服 HIF-PHI,用于治疗非透析的成年慢性肾脏病患者的贫血。该产品采用口服给药,因此有望提高患者的治疗依从性,满足慢性肾病贫血领域未得到满足的治疗需求,包括透析和非透析患者。
  • 该产品的中国三期试验已显示出积极的结果。主要终点表明,Desidustat在提高血红素水平方面比安慰剂更有效。
  • 目前,CMS的4种创新药物已进入商业化阶段。同时,Desidustat Tablets等产品的临床开发和注册流程的持续推进有望丰富集团上市的创新产品组合,并为集团的可持续健康发展带来新的推动力。

China Medical System Holdings Limited ("CMS" or the "Group") is pleased to announce that on 22 April 2024, the New Drug Application (NDA) of Desidustat Tablets ("Desidustat Tablets" or the "Product") has been accepted by the National Medical Products Administration of China (NMPA). The Product is a novel, oral Hypoxia-Inducible Factor-Prolyl Hydroxylase Inhibitor (HIF-PHI) for treating anaemia in non-dialysis adult, Chronic Kidney Disease (CKD) patients.

中国医疗集团控股有限公司(“CMS” 或 “集团”)欣然宣布,2024年4月22日,德西杜司特片剂(“德西杜司特片剂” 或 “产品”)的新药申请(NDA)已获得中国国家药品监督管理局(NMPA)的受理。该产品是一种新型的口服缺氧诱导因子-脯氨酰羟化酶抑制剂(HIF-PHI),用于治疗非透析成人、慢性肾脏病(CKD)患者的贫血。

CKD involves the gradual loss of functioning of kidneys and eventually leads to kidney failure. If kidneys are healthy, they will naturally secrete beneficial levels of a hormone called Erythropoietin (EPO), which encourages red blood cell production. If the kidneys are impaired, they will produce reduced levels or tire of EPO production completely, leading to anaemia. HIF-PHI promotes erythropoiesis through increasing endogenous erythropoietin, improving iron availability and reducing hepcidin.

慢性肾脏病涉及肾脏功能逐渐丧失,最终导致肾功能衰竭。如果肾脏健康,它们会自然分泌一种有益水平的名为促红细胞生成素(EPO)的激素,这种激素可促进红细胞的产生。如果肾脏受损,它们产生的EPO水平会完全降低或减少,从而导致贫血。HIF-PHI 通过增加内源性促红细胞生成素、提高铁利用率和减少铁西汀来促进红细胞生成。

It is estimated that more than 120 million people are living with CKD in China[1]. Anaemia is one of the frequent complications of CKD. A survey in China showed that the prevalence of anaemia in patients at CKD stage 1 to 5 were 22.0%, 37.0%, 45.4%, 85.1%, and 98.2%, respectively[2]. The target-achieving rate (the haemoglobin (Hb) level reaching the target value (110~120g / L)) was only 8.2% for anaemia patients in non-dialysis CKD and 35.2% for haemodialysis CKD, showing a large unmet healthcare need[3].

据估计,中国有超过1.2亿CKD患者[1]。贫血是 CKD 的常见并发症之一。中国的一项调查显示,慢性肾病1至5期患者的贫血患病率分别为22.0%、37.0%、45.4%、85.1%和98.2%[2]。非透析CKD的贫血患者的目标实现率(血红蛋白(Hb)水平达到目标值(110~120g/L))仅为8.2%,血液透析CKD的目标实现率为35.2%,显示出大量未得到满足的医疗需求[3]

China Phase III trial of the Product has demonstrated positive results. The primary endpoint of the Hb mean change from baseline to the period of Week 7-9 has indicated that, Desidustat is more effective than placebo in increasing Hb level. The least squares mean and 95% CI of Hb change from baseline to the period of Week 7-9, using covariance model analysis, has shown an increase of 16.38 g/l [95%CI: 14.50, 18.26] in the Desidustat group and a decrease of 1.13 g/l [95%CI: -3.68, 1.41] in the placebo group, for a between-group difference of 17.52 g/l [95%CI:14.353, 20.681], with the lower limit of 95% CI above 0.

该产品的中国三期试验已显示出积极的结果。从基线到第7-9周Hb平均值变化的主要终点表明,Desidustat在提高血红蛋白水平方面比安慰剂更有效。使用协方差模型分析,从基线到第7-9周期间,Hb的最小二乘均值和95%置信区间变化显示,Desidustat组增加了16.38 g/l [95% CI:14.50,18.26],安慰剂组下降了1.13 g/l [95% CI: -3.68,1.41],组间差为17.52 g/l [95% CI: 14.353,20.681],95% 置信区间的下限高于 0。

The Product is administrated orally, thus expecting to improve the treatment compliance of patients and to meet the unmet treatment needs in the field of CKD anaemia, including both dialysis and non-dialysis patients. Desidustat Tablets have been approved for marketing in India.

该产品采用口服给药,因此有望提高患者的治疗依从性,满足慢性肾病贫血领域未得到满足的治疗需求,包括透析和非透析患者。Desidustat平板电脑已获准在印度上市。

CMS INTERNATIONAL DEVELOPMENT AND MANAGEMENT LIMITED, a wholly-owned subsidiary of the Group, obtained an exclusive license for the Product from Zydus Lifesciences Limited (earlier known as Cadila Healthcare Limited) on 20 January 2020.

集团的全资子公司CMS国际开发与管理有限公司于2020年1月20日从Zydus Lifesciences Limited(前身为卡迪拉医疗有限公司)获得该产品的独家许可。

Reference:

参考文献:

  1. ZhangL, WangF, WangL, et al. Prevalence of chronic kidney disease in China: a cross-sectional survey[J]. Lancet, 2012, 379(9818):815-822. DOI: 10.1016/S0140-6736(12)60033-6
  2. Chinese expert consensus on diagnosis and therapy of renal anaemia (the 2014 revised edition), Chinese Journal of Nephrology, 2014;30:712-716
  3. Chinese expert consensus on diagnosis and therapy of renal anaemia (the 2018 revised edition), Chinese Journal of Nephrology, 2018, 34(11): 860-866
  1. 张L,王夫,王L,等中国慢性肾脏病患病率:横断面调查 [J].柳叶刀,2012,379(9818):815-822。DOI:10.1016/S0140-6736 (12) 60033-6
  2. 中国肾脏贫血诊断与治疗专家共识(2014 年修订版),《中国肾脏病杂志》,2014;30:712-716
  3. 中国肾贫血诊断和治疗专家共识(2018年修订版), 《中国肾脏病杂志》,2018, 34 (11): 860-866

CMS Disclaimer and Forward-Looking Statements
This press release is not intended to promote any products to you and is not for advertising purposes. This press release does not recommend any drugs, medical devices and/or indications. If you want to know more about the diagnosis and treatment of specific diseases, please follow the opinions or guidance of your doctor or other medical and health professionals. Any treatment-related decisions made by healthcare professionals should be based on the patient's specific circumstances and in accordance with the drug package insert.

CMS 免责声明和前瞻性声明
本新闻稿无意向您推广任何产品,也不用于广告目的。本新闻稿不推荐任何药物、医疗器械和/或适应症。如果您想进一步了解特定疾病的诊断和治疗,请遵循您的医生或其他医疗和卫生专业人员的意见或指导。医疗保健专业人员做出的任何与治疗相关的决定都应基于患者的具体情况并符合药物包装说明书。

This press release which has been prepared by CMS does not constitute any offer or invitation to purchase or subscribe for any securities, and shall not form the basis for or be relied on in connection with any contract or binding commitment whatsoever.

本新闻稿由CMS编写,不构成购买或认购任何证券的任何要约或邀请,不得构成任何合同或具有约束力的承诺的基础或依据。

Media Contact

媒体联系人

Brand: China Medical System Holdings Ltd.

品牌:中国医疗系统控股有限公司

Contact: CMS Investor Relations

联系人:CMS 投资者关系部

Email: ir@cms.net.cn

电子邮件:ir@cms.net.cn

Website:

网站:

Source: China Medical System Holdings Ltd.

来源:中国医疗系统控股有限公司


声明:本内容仅用作提供资讯及教育之目的,不构成对任何特定投资或投资策略的推荐或认可。 更多信息
    抢沙发