SQUEEZE - Maximising Impact of Prescription Drugs in Rheumatoid Arthritis
SQUEEZE - 最大限度地发挥处方药对类风湿关节炎的作用
基本信息
- 批准号:10055567
- 负责人:
- 金额:$ 177.28万
- 依托单位:
- 依托单位国家:英国
- 项目类别:EU-Funded
- 财政年份:2022
- 资助国家:英国
- 起止时间:2022 至 无数据
- 项目状态:未结题
- 来源:
- 关键词:
项目摘要
The SQUEEZE consortium comprehensively addressed how biomarkers can be used to optimize disease modifying antirheumatic drugs (DMARDs) for rheumatoid arthritis (RA). RA is a chronic immune-mediated disease with enormous health-related quality of life and socioeconomic impact. A broad choice of DMARDs with different targets is up to date available in clinical care, however without sufficient markers indicating the best choice for a particular patient, treatment strategies can be ineffective, cumbersome and expensive. The team of leading academic centres with a first-class record in translational and clinical research, together with patients and small and medium sized enterprises (SMEs) has set out to deliver a collaborative programme to advance the clinical application of biomarkers to improve benefit, safety, and value of approved DMARDs. SQUEEZE utilizes models from data science, clinical trials, translational science, and behavioural science to engage in a complementary, synergistic, and non-overlapping manner addressing the use of biomarkers to improve the ability to select the DMARD with the highest likelihood of fitting the immunophenotypic and clinical profile of the patient, to optimise dose and route of existing DMARDs; and to inform an innovative model of care focusing on patient ´s preferences and needs to increase adherence to prescribed drugs. Through nine dedicated work packages SQUEEZE integrates to validate clinical, laboratory, molecular, digital and behavioural biomarkers to enable the recognition of patients with high likelihood of response to treatment and the selection of the drug with highest chance of benefit for an individual patient; and as such improve efficacy and safety of existing therapies (by squeezing the most out of existing drugs) in synergy with other EU-wide activities.
SQUEEZE联盟全面阐述了生物标志物如何用于优化类风湿关节炎(RA)的疾病缓解抗风湿药物(DMARD)。RA是一种慢性免疫介导的疾病,对健康相关的生活质量和社会经济影响巨大。具有不同靶点的DMARD的广泛选择在临床护理中是最新的,然而,如果没有足够的标志物指示特定患者的最佳选择,治疗策略可能是无效的,繁琐的和昂贵的。在转化和临床研究方面具有一流记录的领先学术中心团队,与患者和中小型企业(SME)一起,已着手提供一项合作计划,以推进生物标志物的临床应用,以提高已批准的DMARD的获益,安全性和价值。SQUEEZE利用来自数据科学、临床试验、转化科学和行为科学的模型,以互补、协同和非重叠的方式解决生物标志物的使用问题,以提高选择最有可能符合患者免疫表型和临床特征的DMARD的能力,优化现有DMARD的剂量和途径;并提供一种创新的护理模式,重点关注患者的偏好和需求,以提高对处方药物的依从性。通过9个专门的工作包,SQUEEZE整合了临床、实验室、分子、数字和行为生物标志物的验证,以识别对治疗有高反应可能性的患者,并选择对个体患者有最大获益机会的药物;因此,与欧盟范围内的其他活动协同,提高现有疗法的疗效和安全性(通过最大限度地利用现有药物)。
项目成果
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其他文献
吉治仁志 他: "トランスジェニックマウスによるTIMP-1の線維化促進機序"最新医学. 55. 1781-1787 (2000)
Hitoshi Yoshiji 等:“转基因小鼠中 TIMP-1 的促纤维化机制”现代医学 55. 1781-1787 (2000)。
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LiDAR Implementations for Autonomous Vehicle Applications
- DOI:
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2021 - 期刊:
- 影响因子:0
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吉治仁志 他: "イラスト医学&サイエンスシリーズ血管の分子医学"羊土社(渋谷正史編). 125 (2000)
Hitoshi Yoshiji 等人:“血管医学与科学系列分子医学图解”Yodosha(涉谷正志编辑)125(2000)。
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Effect of manidipine hydrochloride,a calcium antagonist,on isoproterenol-induced left ventricular hypertrophy: "Yoshiyama,M.,Takeuchi,K.,Kim,S.,Hanatani,A.,Omura,T.,Toda,I.,Akioka,K.,Teragaki,M.,Iwao,H.and Yoshikawa,J." Jpn Circ J. 62(1). 47-52 (1998)
钙拮抗剂盐酸马尼地平对异丙肾上腺素引起的左心室肥厚的影响:“Yoshiyama,M.,Takeuchi,K.,Kim,S.,Hanatani,A.,Omura,T.,Toda,I.,Akioka,
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{{ truncateString('', 18)}}的其他基金
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2901954 - 财政年份:2028
- 资助金额:
$ 177.28万 - 项目类别:
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$ 177.28万 - 项目类别:
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- 批准号:
2908693 - 财政年份:2027
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$ 177.28万 - 项目类别:
Studentship
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2908917 - 财政年份:2027
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$ 177.28万 - 项目类别:
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$ 177.28万 - 项目类别:
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2890513 - 财政年份:2027
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$ 177.28万 - 项目类别:
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$ 177.28万 - 项目类别:
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2876993 - 财政年份:2027
- 资助金额:
$ 177.28万 - 项目类别:
Studentship
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