Drug Development

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课程主页: https://www.coursera.org/archive/drug-development

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University of California, San Diego

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The University of California San Diego, Skaggs School of Pharmacy and Pharmaceutical Sciences Drug Development course brings you lectures from both faculty and industry experts. With this course, recorded on campus at UCSD, we seek to share our access to top people in the field who bring an unprecedented range of expertise on drug development. In this course you will learn the different stages of clinical development as well as the regulatory including but not limited to, an Investigational New Drug Application (IND), New Drug Application (NDA), and product labeling. Additionally you will learn how to Incorporate study design methods for consideration in the design of clinical protocols to assess safety, tolerability, and efficacy in multiple therapeutic areas. In this course you will learn the different phases of clinical development: * Phase 1 or early stage clinical trial are conducted primar­ily to determine how the new drug works in humans, its safety profile and to predict its dosage range. It typically involves between 30 and 100 healthy volunteers. * Phase 2 or Proof of Concept POC studies test for efficacy as well as safety and side effects in a group of between 30 to 200 hundred patients with the disease for which the new drug is being developed. * Phase 3 or late stage clinical development involve much larger group of patients, between a few hundred to thousands, depending on the indication, which will help determine if the new drug can be considered both safe and effective. It will involve control groups using placebo and/or current treatment as a comparison. * Product registration and approval process after a drug is considered safe and effective from Phase 3 trials, it must be authorized in each individual country before it can be marketed. All data gen­erated about the small molecule or biologic is collected and submitted to the regulatory authorities in the US at the FDA, Food and Drug Administration FDA, in Europe the EMA or European Medicines Agency, Japan Ministry of Health and other countries which may require their own national approvals. This course is intended as part 2 of a series: Drug Discovery (https://www.coursera.org/learn/drug-discovery), Drug Development and Drug Commercialization (https://www.coursera.org/learn/drug-commercialization). We would highly recommend that you take the courses in order since it will give you a better understanding on how a drug is discovered in the lab before being tested in clinical trials and then launched in the market place.

药物开发:加利福尼亚大学圣地亚哥分校的斯卡格斯药学院和药物科学学院药物开发课程为您带来了来自教师和行业专家的演讲。通过本课程,该课程记录在UCSD的校园中,我们力求与那些在药物研发领域拥有空前专业知识的顶尖人才分享我们的访问机会。 在本课程中,您将学习临床开发的不同阶段以及法规,包括但不限于新药研究性新申请(IND),新药应用(NDA)和产品标签。此外,您还将学习如何将研究设计方法纳入临床方案的设计中,以评估多个治疗领域的安全性,耐受性和功效。 在本课程中,您将学习临床开发的不同阶段: *主要进行第一阶段或早期临床试验,以确定新药如何在人体中发挥作用,其安全性并预测其剂量范围。它通常涉及30至100名健康志愿者。 *第2阶段或概念验证POC研究针对30至200例正在开发新药的疾病的患者进行功效,安全性和副作用的测试。 *根据适应症,三期或晚期临床开发涉及的患者群体要大得多,几百到几千之间,这将有助于确定新药是否可以被认为既安全又有效。对照组将使用安慰剂和/或当前治疗作为对照。 *在第三阶段试验中认为某药物安全有效后,产品注册和批准流程必须在每个国家/地区获得授权,然后才能销售。收集有关小分子或生物制剂的所有数据,并提交给美国食品药品管理局(FDA),食品和药物管理局(FDA),欧洲EMA或欧洲药品管理局,日本厚生省和其他可能要求其拥有国家认可。 本课程是该系列课程的第2部分:药物发现(https://www.coursera.org/learn/drug-discovery),药物开发与药物商业化(https://www.coursera.org/learn/drug -商业化)。我们强烈建议您按顺序学习这些课程,因为这样可以使您更好地了解在临床试验中测试药物然后在市场上投放之前如何在实验室发现药物。

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