Identifying Industry Margins with Price Constraints: Structural Estimation on Pharmaceuticals
American Economic Review 2018, 108(12): 3685–3724 https://doi.org/10.1257/aer.20140202
with Pierre Dubois
This paper develops a structural model to investigate the effects of pharmaceutical price regulation on demand and on manufacturers' price-setting behavior in France. We estimate price-cost margins in a regulated market with price constraints and infer whether these constraints are binding. Once the shape of demand is recovered, the identification strategy exploits cost restrictions across drugs, which come from observing the same drugs in potentially price-constrained markets (France) and in markets where prices are unregulated (the US and Germany). Using data on the anti-ulcer market from 2003 to 2013, we find that some drugs are significantly constrained by regulation. Counterfactual simulations suggest that price constraints generated some modest savings (approximately 2% of total expenses) and increased consumer surplus, relative to a free pricing scenario. These effects come from shifting consumption towards branded drugs at the expense of generics. However, a policy defining price caps based on prices in other countries (external reference pricing) would increase generic penetration and generate additional savings and consumer surplus by reducing all prices, particularly those of generics.
Delisting of Pharmaceuticals from Insurance Coverage: Effects on Consumption, Pricing and Expenditures in France
Working paper
This work structurally estimates the impact on demand and supply of public insurance coverage of pharmaceuticals and its removal (so-called delisting). The analysis focuses on the 2008 delisting of oral phlebotonics (drugs to treat venous circulation disorders) in France, where insurance coverage is tied to price regulation: when a drug is delisted, its price becomes unregulated and the manufacturer can set it freely. This regulatory change and the fact that some drugs were never covered before 2008 provide the variation needed to identify price-cost margins and simulate the counterfactual pricing equilibrium without coverage and price regulation. Results suggest that insurance coverage with price regulation stabilizes prices and guarantees demand for some drugs, like generics, which would sell much less in the absence of coverage. Without insurance coverage and price regulation, increased competition and higher price elasticity would result in lower average prices and reduce demand for most drugs on the market, in line with what is observed after 2008 at the delisting or oral phlebotonics.
Stigma as a barrier to treatment and adoption of innovation
with Laura Grigolon
Working paper
Diseases such as mental illnesses, HIV, or certain cancer types carry a stigma that may deter patients from seeking treatment and, in turn, hinder the diffusion of innovative therapies. We investigate the link between social stigma as a barrier to access treatment and the adoption of innovation using the population of patients diagnosed with advanced lung cancer in Ontario (Canada) over the last decade: among all cancers, lung cancer suffers most from stigma because of its association with smoking behavior. Thanks to the rich information on patients at the geographic level, we are able to incorporate social stigma in a model of patient's utility for pursuing treatment. We find that patients face significant stigma acting as a barrier to treatment participation, which in turn slows down the adoption of innovative lung cancer treatment. Removing social stigma would increase the use of innovative treatment by 4%, with benefits in survival outweighing the additional treatment costs.
Prescription of Generics: Evidence from France
Working paper
This work investigates the factors that enter the prescription decision between brand-name and generic drugs, to verify whether physicians adjust the choice of the brand type to patients preferences and characteristics. The aim is to shed some light on the still limited generic prescription in France and on the documented increase in sales for brand-name drugs subject to reference pricing. The analysis uses CEGEDIM data on a representative sample of 326 French General Practitioners and up to 7,500 patients, receiving prescriptions between 2000 and 2008 for drugs in five therapeutic classes (anti-ulcer, anti-diabetes, anti-hypertensive, anti-cholesterol and antidepressant drugs). Results suggest that physicians and patients characteristics play a major role in explaining the decision on the brand type: patients that are fully reimbursed show a higher probability of receiving a brand-name prescription. In addition, the probability of generic prescription drops significantly once a drug is subject to reference pricing, but out of pocket expenses for drugs with a price higher than the reference price discourage brand-name prescription.
Geographic disparities in access to cancer treatment and health outcomes in Ontario
with Laura Grigolon and William Evans
Optimal formulary choices in Medicare Part D
with Alessandro Iaria and Léa Bignon
Collusion in the US generic drug market
with Rob Clark and Chris Fabiilli