Insider Trading in the Clinical Trial Setting

A. Horwich, Crista M. Brawley
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引用次数: 0

Abstract

The Securities and Exchange Commission’s enforcement agenda regularly includes charges of trading based on material nonpublic information about a clinical drug trial conducted to obtain FDA approval to market a new drug. Almost half of the recent cases have been accompanied by a criminal indictment. In an academic setting, researchers and those who advise them, unlike employees of public companies, are not generally given training about the risks of securities trading. Recent developments in the law might be applied in connection with clinical trial information in ways that would not have been foreseen until recently. It is time for a comprehensive analysis of how the law of insider trading may be applied to the important endeavor of clinical drug trials. Clinical trials should not be sullied by conflicts created by unlawful trading. This Article begins with the basic principles of insider trading, followed by a summary of how clinical trials are conducted and regulated. It then turns to the ways in which nonpublic information material to the stock price of the sponsor of the trial might be used to trade or tip. The analysis that follows identifies a number of situations where use or disclosure of material nonpublic information about a trial could be unlawful. Employees of sponsors of the trial, clinical investigators, and even the subjectsparticipating in a trial could run afoul of the prohibition on insider trading, such as when information has been used in breach of a confidentiality agreement or exchanged between an investigator and a trial participant, exchanged among trial participants, gleaned from attending medical conferences, and obtained in other settings specific to this industry. Presenting the full potential reach of the law facilitates taking steps to avoid violating the law. The analysis demonstrates that anyone involved in a clinical drug trial must be attuned to the risks of misusing material nonpublic information, including in scenarios not yet pursued by the SEC. By understanding the potential reach of the law, those involved in or who learn information about a specific trial can take steps to avoid or minimize the risk of liability. The Article concludes with recommendations to achieve this end. The Article thus presents a complete case study of an industry-specific application of insider trading law, with recommendations that can be applied to other industries.
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临床试验环境中的内幕交易
美国证券交易委员会(Securities and Exchange Commission)的执法议程经常包括根据有关临床药物试验的重大非公开信息进行交易的指控,该试验旨在获得美国食品药品监督管理局(FDA)的新药上市批准。在最近发生的案件中,几乎有一半附有刑事起诉书。在学术环境中,与上市公司的员工不同,研究人员和顾问通常不会接受有关证券交易风险的培训。法律的最新发展可能会以直到最近才预见到的方式适用于临床试验信息。现在是时候全面分析内幕交易法如何适用于临床药物试验的重要努力了。临床试验不应被非法交易造成的冲突所玷污。本文从内幕交易的基本原则开始,然后总结临床试验是如何进行和监管的。然后,它转向了与试验赞助商股价有关的非公开信息材料可能被用于交易或提示的方式。以下分析确定了使用或披露有关审判的重大非公开信息可能是非法的一些情况。试验发起人、临床研究人员的员工,甚至试验参与者的员工,都可能违反禁止内幕交易的规定,例如当信息被用于违反保密协议,或在研究人员和试验参与者之间交换,在试验参与者之间交流,从参加医学会议中收集,并在该行业特定的其他设置中获得。充分展示法律的潜在影响有助于采取措施避免违法。分析表明,任何参与临床药物试验的人都必须意识到滥用重大非公开信息的风险,包括在美国证券交易委员会尚未采取行动的情况下。通过了解法律的潜在影响范围,参与或了解特定试验信息的人可以采取措施避免或最大限度地降低责任风险。该条最后提出了实现这一目的的建议。因此,本文对内幕交易法在特定行业的适用进行了完整的案例研究,并提出了适用于其他行业的建议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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