Expert Review of Pharmacoeconomics & Outcomes Research · 2020 · 15 citations · 17 references
PharmacyPharmaceutical PolicyPharmacoeconomicsCost-minimization AnalysisPharmaceutical CompliancePrecision MedicineAccess To MedicinesEssential MedicinesMedication AffordabilityNew Drug ApplicationsPharmaceutical EconomicsPharmaceutical MarketingCoverage For Off-label UseGeneric Drug ApplicationsGeneric Drug PricingIncremental Innovation ManagementMarket Exclusivity PolicyPharmaceutical Innovation StrategyPrescribing PracticesPrice Premium Effects
INTRODUCTION: Pharmaceutical research and development (R&D) is costly and only a minority of patients can access innovative medicines due to affordability constraints. Value-added medicines (VAMs) can offer potential benefits at significantly lower R&D costs. AREAS COVERED: VAMs may address different health care needs and problems, including off-label use of medicines, poor patient adherence, problems related to polypharmacy, need for home and/or personalized health care services. However, several barriers prevent societies from maximizing the benefits of incremental innovation related to VAMs. Generic manufacturers have limited budget and experience to demonstrate the value of new VAMs. Current market exclusivity options do not efficiently exclude freeridership and do not guarantee a return on investment for VAM innovators. Value propositions of VAMs are limitedly consistent with current HTA frameworks, consequently, incremental innovation is not acknowledged, nor rewarded with differential pricing by payers. Moreover, VAMs are often perceived solely as generic medicines by prescribers. EXPERT OPINION: Current practices may need to be reconsidered to exploit the full societal benefit of VAMs, including more efficient policies to guarantee market exclusivity for incremental innovation, acknowledgment of a fair price premium based on a specific value framework and the acceptance of low-cost evidence generation methods.
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