\documentclass[../Main.tex]{subfiles} \graphicspath{{\subfix{Assets/img/}}} \begin{document} This paper sits within an intersection of health and industrial organization economics that is frequently studied. Encouraging a strong supply of novel and generic pharmaceuticals contributes in important ways to both public health and fiscal policy. Not only to the pathway to drug approval long, as many as 90\% of compounds that begin human trials fail to gain approval (\cite{khmelnitskaya_competition_2021}). Complicating this is the complex regulatory and competitive environment in which pharmaceutical companies operate. %%%%%%%%% Why are drugs so expensive? % van der Grond, Uyle-de Groot, Pieters 2017 % - What causes high costs of drugs? % - High level synthesis of discussion regarding causes % - Academic and non-academic sources %%%%%%%%%%%%%%%% What do we know about clinical trials? % Hwang, Carpenter, Lauffenburger, et al (2016) % - Why do investigational new drugs fail during late stage trials? \citeauthor{hwang_failure_2016} (\citeyear{hwang_failure_2016}) investigated causes for which late stage (Phase III) clinical trials fail across the USA, Europe, Japan, Canada, and Australia. They found that for late stage trials that did not go on to recieve approval, 57\% failed on efficacy grounds, 17\% failed on safety grounds, and 22\% failed on commercial or other grounds. For context, this current work hopes to be able to distinguish some of the mechanisms behind those commercial or other failures. % Abrantes-Metz, Adams, Metz (2004) % - What correlates with successfully passing clinical trials and FDA review? % - In \citeyear{abrantes-metz_pharmaceutical_2004}, \citeauthor{abrantes-metz_pharmaceutical_2004} described the relationship between various drug characteristics and how the drug progressed through clinical trials. This non-causal estimate was notable for using a mixed state proportional hazard model and estimating the impact of observed characteristics in each of the three phases. They found that as trials last longer, the rate of failure increases for Phase I \& II trials, while Phase 3 trials generally have a higher rate of success than failure after 91 months. % Ekaterina Khmelnitskaya (2021) % - separates scientific from market failure of the clinical drug pipeline In her doctoral dissertation, Ekaterina Khmelnitskaya studied the transition of drug candidates between clinical trial phases. Her key contribution was to find ways to disentangle strategic exits from the development pipeline and exits due to clinical failures. She found that overall 8.4\% of all pipeline exits are due to strategic terminations and that the rate of new drug production would be about 23\% higher if those strategic terminatations were elimintated (\cite{khmelnitskaya_competition_2021}). % causal separation of strategic exits etc. % Waring, Arrosmith, Leach, et al (2015) % - Atrition of drug candidates from four major pharma companies % - Looked at how phisicochemical properties affected clinical failure due to safety issues %not in this version %%%%%%%%% What do we know about drug development incentives? % Dranov, Garthwaite, and Hermosilla (2022) % - does the demand-pull theory of R&D explain novel compound development? % - no, it is biased towards follow-on drug R&D. % Acemoglu and Linn % - Market size in innovation % - Exogenous demographic trends has a large impact on the entry of non-generic drugs and new molecular entitites. On the side of market analysis, %TODO:remove when other sections are written up. \citeauthor{acemoglu_market_2004} (\citeyear{acemoglu_market_2004}) used exogenous deomographics changes to show that the entry of novel compounds is highly driven by the underlying aged population. They estimate that a 1\% increase in applicable demographics increase the entry of new drugs by 6\%, mostly concentrated among generics. Among non-generics, a 1\% increase in potential market size (as measured by demographic groups) leads to a 4\% increase in novel therapies. % Gupta % - Inperfect intellectual property rights in the pharmaceutical industry %\cite{GupaPhd2023} % Agarwal and Gaule 2022 % - Retrospective on impact from COVID-19 pandemic % Not in this version \end{document}