孤儿药认定对制药生物技术公司IPO投资者有价值的无形资产

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引用次数: 0

摘要

实施了孤儿药立法,并提供了监管和财政激励措施,以鼓励治疗罕见病的药物创新。本研究旨在检验美国食品药品监督管理局(FDA)授予制药和生物技术初创公司的OD指定(ODD)是否可以被视为在美国股票市场首次公开发行(IPO)时吸引创业融资和增加投资金额的相关信号。此外,上市前的ODD也可能影响初创公司在IPO前获得其他相关资源,例如风险投资、合作收入和员工。我们发现,对于股票市场的IPO投资者而言,ODD的信号能力具有显著的正统计学意义:IPO前的ODD增加了约37.5%的IPO收益。回归结果还表明,在公司上市前,ODD比其他申请更能吸引IPO投资者和其他有价值的资源。从信号理论和药物开发政策的角度讨论了学者和政策的影响
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Orphan Drug Designations as Valuable Intangible Assets for IPO Investors in Pharma-Biotech Companies
Orphan Drug (OD) legislation has been implemented with regulatory and financial incentives to encourage the drug innovation to treat rare diseases. This study aims to test whether OD Designations (ODD) granted by the Food and Drug Administration (FDA) to pharmaceuticals and biotechnology start-up companies may be considered as relevant signals in, attracting entrepreneurial finance and increasing the amount invested at the time of the Initial Public Offering (IPO) in the US stock markets. Furthermore, ODD before going public may also influence the access to other relevant resources for start-ups companies as for instance venture capital investments, collaborative revenues and employees prior to IPO. We found that the signaling power of ODD is positively and statistically significant for IPO investors in stock markets: an ODD prior to an IPO increase the IPO proceeds by about 37,5%. Regression results also suggest that ODD are stronger than p tents applications to attract IPO investors and other valuable resources before that the company goes public. Scholar and policy implications are discussed in the light of the signaling theory and drug development policies
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