药品
药物开发
抗癌药物
医学
癌症
批准的药物
投资(军事)
新药申请
临床试验
药理学
风险分析(工程)
业务
重症监护医学
内科学
法学
政治
政治学
作者
Ajaikumar B. Kunnumakkara,Devivasha Bordoloi,Bethsebie Lalduhsaki Sailo,Nand Kishor Roy,Krishan Kumar Thakur,Kishore Banik,Mehdi Shakibaei,Subash C. Gupta,Bharat B. Aggarwal
标识
DOI:10.1177/1535370219839163
摘要
The success rate for cancer drugs which enter into phase 1 clinical trials is utterly less. Why the vast majority of drugs fail is not understood but suggests that pre-clinical studies are not adequate for human diseases. In 1975, as per the Tufts Center for the Study of Drug Development, pharmaceutical industries expended 100 million dollars for research and development of the average FDA approved drug. By 2005, this figure had more than quadrupled, to $1.3 billion. In order to recover their high and risky investment cost, pharmaceutical companies charge more for their products. However, there exists no correlation between drug development cost and actual sale of the drug. This high drug development cost could be due to the reason that all patients might not respond to the drug. Hence, a given drug has to be tested in large number of patients to show drug benefits and obtain significant results.
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