Incentives for Clinical Trials
نویسندگان
چکیده
Who gains from more information on the quality of pharmaceutical drugs? Are there incentives for voluntary post-approval clinical trials among pharmaceutical companies? Contrary to popular belief, this paper shows that it is not in the consumer interest that clinical evidence establishing the relative e¤ectiveness within a class of drugs are produced. Pharmaceutical companies, on the other hand, do bene t: the elimination of uncertainty regarding quality increases expected product di¤erentiation, thereby raising prices for both high-quality and low-quality drugs, to the disadvantage of consumers. Still there is no unique equilibrium where the market provides clinical trials. If the costs of carrying out clinical trials are small, in relative terms, there will be a coordination problem between rms, as rms will want a rival rm to carry the cost. If the costs are large they will be prohibitive. Legislation that obligates entering rms to carry out post-approval trials is bene cial for rms if it solves the coordination problem, but is otherwise harmful. Legislation is never in the interest of consumers. Key words: Quality uncertainty, Symmetric information, Pharmaceutical market, Clinical trial JEL-codes: D81, D83, I18, L15 Centre for Health Economics, Department of Economics, Stockholm School of Economics, P.O. Box 6501, SE-113 83 Stockholm, Sweden, e-mail: [email protected] Pharmaceutical Bene ts Board, P.O. Box 55, SE-171 11 Solna, Sweden, e-mail: [email protected]
منابع مشابه
مرور ملاحظات اخلاقی و نقد میزان خطر قابل قبول در کارآزمایی بالینی بر داوطلب سالم
Healthy volunteers are the first group who take part in experimental studies on the efficacy of new drugs. Parallel with expanding the boundaries of medical science, medical research has shown rapid growth which has caused new and critical ethical challenges in medical research.A clinical trial is one of the essential methods in clinical research and a very challenging method from the ethical v...
متن کاملClinical Trials: the Effects of Registries and Results Databases∗
We analyze the incentives of pharmaceutical firms to generate scientific knowledge through clinical trials and how these incentives are affected through different regulatory environments. We propose a formal model of a pharmaceutical firm’s investment in clinical trials. Our model can explain why voluntary trial registries could not solve the problem of selective reporting of trial results. We ...
متن کاملCost-effectiveness of health research study participant recruitment strategies: a systematic review.
BACKGROUND A large fraction of the cost of conducting clinical trials is allocated to recruitment of participants. A synthesis of findings from studies that evaluate the cost and effectiveness of different recruitment strategies will inform investigators in designing cost-efficient clinical trials. PURPOSE To systematically identify, assess, and synthesize evidence from published comparisons ...
متن کاملTrials, tricks and transparency: how disclosure rules affect clinical knowledge.
Scandals of selective reporting of clinical trial results by pharmaceutical firms have underlined the need for more transparency in clinical trials. We provide a theoretical framework which reproduces incentives for selective reporting and yields three key implications concerning regulation. First, a compulsory clinical trial registry complemented through a voluntary clinical trial results data...
متن کاملCharacteristics of Clinical Trials in Iran: A Sample of 5000 Trials Registered in IRCT
Background and Objectives: A considerable number of clinical trials are conducted in Iran each year. Not much is known about the characteristics of them, this study aimed to investigate key characteristics of Iranian clinical trials. Methods: All clinical trial protocols registered in IRCT until November 2013 were selected. Text mining techniques were used to extract information from data t...
متن کاملMexican-American perspectives on participation in clinical trials: A qualitative study
Clinical trials are essential to advancing knowledge to reduce disease morbidity and mortality; however, ethnic and racial minorities remain under-represented in those studies. We explored knowledge and perceptions of clinical trials among Mexican-Americans in Texas. We conducted focus groups (N = 128) stratified by gender, language preference, and geographical location. This paper presents fou...
متن کامل