Non-alcoholic steatohepatitis (NASH) is rapidly becoming an important public health issue in the top five European markets (France, Germany, Italy, Spain, UK). High prevalence of this multifaceted disease, coupled with a lack of approved pharmacotherapy and novel diagnostics on the horizon, presents a huge opportunity for drug manufacturers. With five agents currently in Phase III trials, and numerous products undergoing Phase II development, a number of highly anticipated launches are likely in the next decade. However, the potential cost of such a drug market will have a substantial impact on the tight healthcare budgets in Europe, such that payers will have to be convinced of the cost-effectiveness of treatments, and manufacturers may have to consider savvy pricing strategies. This research analyzes payer and prescriber perspectives on near-term emerging therapies for NASH, focusing on HTA considerations, reimbursement drivers, product positioning, and uptake potential.
European Access & Reimbursement provides integrated brand-level and country-specific analysis of primary market research conducted with payers and prescribers examining reimbursement dynamics and evaluating the impact of payer policy on prescribing behavior.
France, Germany, Italy, Spain, UK
KEY DRUGS COVERED
Ocaliva, elafibranor, cenicriviroc, selonsertib, vitamin E, pioglitazone, ursodiol, statins, ezetimibe, metformin, SGLT-2 inhibitors, GLP-1 receptor agonists.