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Economics of New Molecular Targeted Personalized Radiopharmaceuticals

机译:新分子有针对性个性化放射性药物的经济学

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Nuclear medicine has come a long way since 2007 when Adrian Nunn pointed out the approval of radiopharmaceuticals was at an all-time low with all the major radiopharmaceutical agents in use having been approved over 10 years ago. Challenges being the prohibitively high cost of drug development and the large number of drugs failing in clinical trials. Proceed to today where molecular imaging is fast-tracking the drug discovery process by reducing both the time and cost to screen candidates by quantitating the drugs effect on the target and toxicity to normal tissues. Nuclear medicine is now leading medical practice in personalized medicine using the theragnostic approach. Theragnostics is defined as the use of molecular diagnostic techniques in real time to stratify patients to guide treatment decisions such as the choice of drug, the dose of administration, and the timing of drug delivery for a given patient. Enabling visualization and quantitation of in vivo function of the whole body and thus patient heterogeneity and variability informs the physician on how to treat an individual patient. Recent successes such as the Food and Drug Administration approval of Lutathera and NETSPOT have resulted in an increasing number of pharmaceutical companies pursing theragnostics further heightened by the purchase of Advanced Accelerator Applications for 3.9 billion by Novartis and Endocyte, Inc for 2.1 billion. Theragnostics are further aiding drug development by showing which agents are most viable and reducing the overall cost of bringing a drug to clinical trials and regulatory approval. This is indeed a renaissance for nuclear medicine in which the acceptance of imaging to inform and monitor therapy has been embraced and even required by the Food and Drug Administration for the clinical evaluation of targeted therapeutic radiopharmaceuticals showing there is indeed a viable business model for targeted theragnostic radiopharmaceuticals and personalized medicine. (C) 2019 Published by Elsevier Inc.
机译:自2007年以来,当阿德里安·纳尼恩指出放射性药物的批准时,核医学已经存在了很长的路要走,在10年前已经批准的所有主要放射性药物代理商处于历史上。挑战是临床试验中的药物开发和大量药物的挑战。前往今天,通过将药物对靶和毒性对正常组织的毒性作用减少来快速跟踪药物发现过程,通过减少筛选的时间和成本来快速跟踪药物发现过程。核医学现在正在使用Theragnostic方法领先的个性化医学医疗实践。 Theragnostics定义为使用分子诊断技术实时使用,分层患者指导治疗决定,例如药物的选择,给药剂量的给药剂量和药物递送的时序。实现全身体内功能的可视化和定量,因此患者的异质性和可变性通知医生如何治疗个体患者。最近的成功,如食品和药物管理局批准的莱特拉和净标题所导致越来越多的药物公司通过购买先进的加速器应用,通过购买高速加速器39亿,诺特人和内核,公司21亿美元。 Theragnostics进一步促进了药物开发,表明哪种药剂最可行,降低将药物带到临床试验和监管批准的总体成本。这确实是核医学的文艺复兴,其中对靶向治疗放射性药物的临床评价而言,甚至是患有针对性的治疗放射性药物的临床评价所需的成像和监测治疗的临床评价所要求的放射性药物和个性化医学。 (c)2019由elsevier公司出版

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