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Payer attitudes to Orphan Drug pricing


Payer Attitudes to Orphan Drug Funding

The explosion of orphan drugs across Europe and the US is pushing healthcare finances towards breaking point according to payers. Requests for orphan drug designation have reached unprecedented levels and the high cost of these specialist treatments is swallowing up a larger and larger share of the drug funding pot. Payers are not happy and clearly something needs to give. But what?

Payer Attitudes to Orphan Drug Funding gives budget-holders a voice. In this report, senior payers from the US and EU5 (France, Germany, Italy, Spain UK) offer insight into the pressures they face and share their ideas about how the current crisis could be addressed.

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The executive summary, taken directly from the report, presents key findings from the research
Research objectives and methodologies employed to produce the report
Detailed report contents
Key themes covered in the report
What you will learn from the report

Executive Summary

Rising interest in orphan drug development
The number of requests for orphan drug designation submitted to the FDA has more than doubled since 2012, and more orphan drugs are reaching the market. Coupled with the trend for high prices, this has led to year-on-year growth in the orphan drugs market outstripping the wider pharmaceutical market. Orphan drug spending now accounts for more than 16 percent of total prescription drug spending.
Pricing is based on what the market will bear
Pharma companies have traditionally justified high prices for orphan drugs because of the cost of development and the need to make a return on investment despite a small number of patients. Payers have tolerated this, but the rising number of treatable rare diseases is placing pressure on resources and the current situation is considered unsustainable.
Payers want fair pricing for orphan drugs
Payers suggest that pharma companies need to more effectively assess the factors dictating the price of orphan drugs. Factors such as the level of innovation and the real cost of development, the size of the patient population that would be eligible for treatment, and the clinical benefits of a drug. Payers indicate a need for a comparative analysis of the overall financial impact of the disease state in terms of the resources used currently, against the resources that will be used with the new drug.
Payers want early engagement from pharma
Payers believe that early engagement with pharma companies regarding orphan drugs in development will help to improve planning, and lower costs as a result. For example, if payers are able to explain their data requirements at a stage when these can influence trial design, this will likely expedite patient access following regulatory approval.
Stakeholder collaboration to increase patient access
Payers highlight several opportunities for collaboration between pharma companies, payers, government, academia, physicians and patients that would be helpful to support patient access. These include information sharing and education, working together to share risk and make orphan drugs more affordable, developing accurate diagnostics to speed reimbursement decisions, and government/university funding for R&D to share the cost of development, thereby reducing pharmas need for high prices.

Doctors Guide Publishing Limited. This executive summary is provided for commercial evaluation purposes only. It can be shared with colleagues for this purpose but cannot be reproduced, extracted or published without the express permission of the publisher.

Research Methodology and Objectives
At a time when payers are questioning the high cost of orphan drugs, expecting more evidence of value, and grappling with tight budgets, this report gives food for thought on how to ensure they are happy and that patients continue to get access to new orphan drugs.

Key questions explored in this report include:

How are pricing decisions made for orphan drugs? Does this differ to non-orphan drugs?
What factors affect how much payers are willing to pay for orphan drugs?
What should pharma consider when pricing orphan drugs?
What key assessment criteria determine funding/reimbursement of an orphan drug?
If the number of eligible patients for an orphan drug increases, should this affect pricing?
Is value-based pricing or conditional reimbursement a way forward for orphan drugs?
When should pharma companies engage with payers on potential new orphan drugs?
How can stakeholders work together to increase patient access to orphan drugs?

Table of Contents

Executive summary

Experts interviewed for this report

Definitions and regulatory environment

Incentives in the US

Incentives in the EU

Market overview

Global Sales of Leading Orphan Drugs, 2014-2016

Payer views on orphan drug pricing

How orphan drugs are priced

United States
United Kingdom
The impact of high prices on the total cost of orphan drugs
Factors pharma should consider when making pricing decisions
Level of innovation and medical need
Patient population and affordability
Pricing implications of an expanded patient population
Level of competition

Payer views on funding and reimbursement

Assessment criteria for reimbursement funding
United States
United Kingdom
Devolved funding and potential inequalities in patient access
US payer views
EU payer views
Limited data available at drug approval
The impact of real-world data post launch

Opportunities for collaboration

Pharma engagement with payers
Stakeholder collaboration to increase patient access
Value-based pricing and conditional reimbursement
Collaboration on orphan drug development funding

More reasons to buy this report
For orphan drugs, the pricing issue isnt new but concern about affordability has reached a whole new level and payers clearly expect the industry to take action. The inexorable tide of big ticket orphan drugs has created an unstainable situation that simply cant be ignored. The development of innovative new orphan drugs has to be paid for somehow; however, there are a host of alternative approaches that could help to address the issues and still give pharma the freedom to continue innovating. Collaboration is the key to a workable solution and that requires all parties to come to the table

This report will enable you to

Understand how orphan drugs are priced in different countries and the cost implications.
Find out why payers believe some high prices are acceptable, and some are not.
Explore the concept of fairness and understand the key factors that prompt concern from payers.
Gain detailed insight into funding and reimbursement decision-making for orphan drugs.
Understand more about the impact of real world data post launch.
Be inspired with new ideas for collaboration and issue resolution across the orphan drugs market.

About FirstWord

FirstWord is an innovative industry intelligence leader serving over 240,000 Pharma and MedTech professionals worldwide. FirstWord offers a range of products and services designed to help your company gain a competitive edge by making key business decisions with speed and confidence.

FirstWord Pharma PLUS is a personalised and comprehensive intelligence service delivering up-to-the-minute pharma news, insight, analysis and expert views of importance to your companys success.
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1. Executive summary
2. Research methodology and objectives
2.1 Experts interviewed for this report
3. Definitions and regulatory environment
3.1 Incentives in the US
3.2 Incentives in the EU
4. Market overview
5. Payer views on orphan drug pricing
5.1 How orphan drugs are priced
5.1.1 United States
5.1.2 France
5.1.3 Germany
5.1.4 Italy
5.1.5 Spain
5.1.6 United Kingdom
5.2 Factors pharma should consider when making pricing decisions
5.2.1 Level of innovation and medical need
5.2.2 Patient population and affordability
5.2.3 Pricing implications of an expanded patient population
5.2.4 Level of competition
6. Payer views on funding and reimbursement
6.1 Assessment criteria for reimbursement funding
6.1.1 United States
6.1.2 France
6.1.3 Germany
6.1.4 Italy
6.1.5 Spain
6.1.6 United Kingdom
6.2 Devolved funding and potential inequalities in patient access
6.2.1 US payer views
6.2.2 EU payer views
6.3 Limited data available at drug approval
6.4 The impact of real-world data post launch
7. Opportunities for collaboration
7.1 Pharma engagement with payers
7.2 Stakeholder collaboration to increase patient access
7.3 Value-based pricing and conditional reimbursement
8. Key takeaways

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Reports Details

Published Date : Aug 2017
Country :Global
Category :Healthcare
Publisher :FirstWord Dossier
Report Delivery By :Email
Report Delivery Time :12 to 24 hours after placing the order.

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