Valuation implications of pharmaceutical companies' R&D regulatory approval notifications

被引:2
|
作者
Hamill, Philip A. [1 ]
McIlkenny, Philip [2 ]
Opong, Kwaku K. [3 ]
机构
[1] Univ Ulster, Sch Business Retail & Financial Serv, Coleraine BT52 1SA, Londonderry, North Ireland
[2] Univ Ottawa, Telfer Sch Management, Ottawa, ON K1N 6N5, Canada
[3] Univ Glasgow, Sch Business, Glasgow G12 8QQ, Lanark, Scotland
来源
BRITISH ACCOUNTING REVIEW | 2013年 / 45卷 / 02期
关键词
Event study; Food and drug administration (FDA); London stock exchange (LSE); New York stock exchange (NYSE); Pharmaceutical firms; Real-options; Research & development (R&D); COMPLEMENTARY ASSETS; INCUMBENTS ADVANTAGE; CORPORATE DISCLOSURE; BIOTECHNOLOGY; INDUSTRY; RETURNS; EXPLORATION; ALLIANCES; COUNTRY; STOCKS;
D O I
10.1016/j.bar.2013.03.004
中图分类号
F8 [财政、金融];
学科分类号
0202 ;
摘要
This paper examines shareholder wealth effects surrounding applications to, and approvals by, the United States Food and Drug Administration (FDA) for firms listed on the New York (NYSE) and London (LSE) stock exchanges. Applications to the FDA for drug approvals significantly increase shareholder wealth for NYSE firms only. The increase is driven by applications for enhancements to existing drugs, with the market anticipating the application, thus suggesting information leakage. FDA approvals also significantly increase shareholder wealth in both markets. However, there is no evidence of information leakage and the significant post-event abnormal returns support the attention-grabbing hypothesis. Enhanced drug approvals are value-relevant for both markets, which highlights the contribution of real-options to firm value. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:99 / 111
页数:13
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