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Psoriasis Pricing, Reimbursement, and Access

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    Report

  • 96 Pages
  • March 2019
  • Region: Global
  • Citeline
  • ID: 4846136
Overview
Launch of multiple IL inhibitors with impressive efficacy has significantly reduced unmet need in the disease, and also provided payers with leverage in price negotiations as they seek to control growing treatment cost.

Key Questions Answered
  • What access controls are payers imposing on biologics in psoriasis?
  • How are biosimilar TNFs impacting the current and future market access for branded drugs?
  • In which markets are payers most likely to leverage growing competition to reduce treatment costs?
  • Which attributes will pipeline agents need to demonstrate to gain competitive advantage in a saturated biologics market?
  • What are payer and physician views on the need for further oral therapies?

Table of Contents

OVERVIEW
REGULATORY LABELS
  • Marketed psoriasis products in the US, Japan, and five major EU markets
  • Bibliography

GLOBAL ACCESS LEVERS
  • Spend on psoriasis biologics is a particular concern for payers
  • High prices of biologics are leading to access barriers and pressure to offer discounts
  • Payers use tenders, physician incentives, and formulary exclusions to drive biosimilar uptake
  • Payers prefer straight discounts to outcomes-based risk agreements

EVIDENCE AND VALUE
  • Payers and physicians regard PASI and DLQI as the most important endpoints
  • Limited scope for differentiation of new agents based on PASI or DLQI
  • Providing treatment holidays or drug-free remissions could differentiate future pipeline treatments
  • Head-to-head trials with active comparators are critical in establishing differentiation
  • Minimum efficacy data of six months needed for good formulary access
  • Six-monthly or annual maintenance dosing regimens may be advantageous for pipeline agents
  • Cardioprotective effect of interleukins remains speculative, but data are welcome
  • Real-world evidence could be used to bolster local or regional positioning in the treatment algorithm

ACCESS TO RECENTLY APPROVED AND PIPELINE DRUGS
  • IL-17 and IL-23 inhibitors are viewed as more efficacious drugs, but TNF-alpha inhibitors will remain first-line biologics
  • IL-23 agents exhibit impressive efficacy but struggle to achieve preferred access versus IL-17s
  • Payers plan to leverage growing competition in the interleukin space through local or regional discounts or contracts
  • Tremfya’s superiority results against Cosentyx will drive prescribing but not pricing or formulary access
  • Siliq’s prospects remain poor, despite no correlation to suicide
  • Dosing frequency is not an important point of differentiation
  • Weaker PASI scores dampen Ilumya’s access prospects
  • Risankizumab’s strong efficacy data boost access prospects, but there is limited scope for a price premium
  • Moderate appetite for an oral inhibitor competitor to Otezla in psoriasis

PRICING
US
  • Insights and strategic recommendations

CANADA
  • Insights and strategic recommendations

JAPAN
  • Insights and strategic recommendations
  • Japan’s pricing strategy is reliant on pricing premiums for innovative medicines
  • Bibliography

FRANCE
  • Insights and strategic recommendations
  • ASMR rating has an impact on pricing
  • Bibliography

GERMANY
  • Insights and strategic recommendations
  • Positive assessment from the G-BA will impact price negotiations
  • Bibliography

ITALY
  • Insights and strategic recommendations
  • Bibliography

SPAIN
  • Insights and strategic recommendations
  • National reimbursement decisions are not a major access barrier in Spain
  • Regional access to psoriasis medicines varies in Spain
  • Bibliography

UK
  • Insights and strategic recommendations
  • NICE approval is a key market access barrier
  • Bibliography

METHODOLOGY
  • Primary research
  • Price assumptions
  • Exchange rates
  • Bibliography

LIST OF FIGURES
Figure 1: Price sources and calculations for the US and EU, by country
LIST OF TABLES
Table 1: Marketed products and approved indications for psoriasis in the US, Japan, and five major EU markets
Table 2: Biosimilar access levers in the US and five major EU markets
Table 3: Levers impacting access to psoriasis drugs in the US and five major EU markets
Table 4: Summary of important key endpoints in psoriasis clinical trial design
Table 5: National reimbursement decisions for marketed and assessed ILs
Table 6: Contracting and financial agreements for interleukins
Table 7: Likely reimbursement for Ilumya in psoriasis
Table 8: Likely reimbursement for risankizumab in psoriasis
Table 9: Pricing of key psoriasis drugs in the US, Japan, and five major EU markets, by country, 2019
Table 10: Pricing premiums given to medicines in Japan that can demonstrate benefit over comparators
Table 11: Transparency Committee’s ASMR ratings and pricing implications
Table 12: Transparency Committee's SMR ratings and pricing implications
Table 13: Spanish Society of Hospital Pharmacy ratings
Table 14: Exchange rates used for calculating drug prices