Abstract

The Canadian system for approval of new cancer drugs is complex with multiple steps. Health Canada grants a license for a drug to be marketed and prescribed. The Canadian Agency for Drugs and Technologies in Health (CADTH) and Institut national d’excellence en santé et services sociaux (INESSS) make recommendations by way of health technology assessments (HTA). If positive, the latter then lead to confidential price negotiations at the pan-Canadian pharmaceutical alliance (pCPA), after which individual provinces and territories make a listing decision. Delays can occur at each stage, but post-HTA delays can be lengthy and unpredictable, denying or impeding access to an effective drug with the potential for devastating clinical outcomes. Conditional funding models have been adopted in a number of European countries with the goal of providing timely access to new medications in areas of unmet need, in advance of further steps in the reimbursement process. This manuscript discusses different stakeholder perspectives on conditional funding agreements—including a recent successful example of such a process in the UK—based on a panel discussion at the 2021 Canadian Association of Population Therapeutics (CAPT) Conference.

Highlights

  • The following summary is based on a panel session delivered at the Canadian Association of Population Therapeutics (CAPT) Conference on 25 October 2021 and is derived from information and insights shared by the presenters

  • Conference topics typically include the disciplines of epidemiology, economics, and policy decision making and beyond; and, the overall 2021 meeting theme was “Evidence in a Time of Crisis”

  • The session’s objective was to discuss how stakeholders can work together to create a system that enables timelier patient access to medications funded by public drug plans, with a specific focus on how a conditional listing mechanism might be a useful tool in promoting patient access in certain instances

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Summary

Introduction

The following summary is based on a panel session delivered at the Canadian Association of Population Therapeutics (CAPT) Conference on 25 October 2021 and is derived from information and insights shared by the presenters. CAPT (https://www.capt-actp.ca/; accessed on 30 December 2021) is a not-for-profit member-driven organization whose participants include scientists and researchers, government, industry and consulting, academia, and the patient community. Conference topics typically include the disciplines of epidemiology, economics, and policy decision making and beyond; and, the overall 2021 meeting theme was “Evidence in a Time of Crisis”. The panel members provided patient, clinician, and industry perspectives on real-world examples and/or the potential value of such a mechanism in the Canadian environment

Background
The UK Experience
Findings
Limitations
Conclusions
Full Text
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