The document discusses approaches to drug pricing and access in various countries. It provides details on Health Canada's proposal for expanded international reference pricing, including the criteria for selecting reference countries. The document also examines the impact of international reference pricing on product introduction delays and launch sequencing. It analyzes mechanisms for price setting and reimbursement across different countries. Finally, it touches on reservation prices in negotiations and Germany's multi-stage process for drug reimbursement decisions.
Listeners participated in a live panel session addressing OHIP+, the recently announced expansion of the Ontario drug program to cover young people who are younger than 25 years-old.
This webinar will introduce you to the Patented Medicine Prices Review Board (PMPRB), how they regulate drug pricing in Canada and the proposed changes that will affect cancer patients.
CAPCA wants to make sure that patients have access to innovative and effective cancer treatments, and Heather Logan, ED of CAPCA, will explain how CAPCA is going to do this and answer your questions about the process. This webinar will introduce you to CAPCA and its mandate and to the new pan-Canadian Cancer Drug Funding Sustainability Initiative (DFSI). The goal of DFSI is to ensure that patients continue to have access to innovative and effective cancer treatments, and that the cancer system is achieving maximum value for money invested.
August 19, 2021 from 1-2 pm
CORD’s LAST SUMMER webinar, Part 1 of our series on “How to Get Back to the PMPRB Original Mandate to prevent excessive drug pricing and support pharma R&D investment.” Learn why responding to the most recent (July 15th) proposed guideline changes is very important.
On August 19, 2021 from 1-2 pm, please JOIN:
When: June 10, 2021
Only 5% of rare diseases have an approved drug therapy. Only 60% of orphan medicines approved by the US FDA or EU EMA are approved in Canada, and often many months or years later. Only 34% of approved orphan medicines are funded by Canadian public drug plans. Under the BEST of circumstances, only 10% of eligible patients get access to an approved medicine. And worldwide, only 1% of rare disease patients will receive an approved drug. Most without treatment are children. How can Canada’s Rare Disease Drug Strategy assure all eligible Canadian patients get access to the most appropriate medicine for their individual needs?
Two panels will be tasked to consider a “Canada Leading the Way” strategic pharmaceutic framework that (1) attracts early investment in R&D; (2) reduces and manages risk for early adoption of innovative therapies; and (3) leads to a sustained culture of collaboration and trust among all stakeholders, including regulators, industry, payers, and patients. In particular, what has Canada learned from addressing COVID, for example, in terms of screening, diagnosis, drug repurposing, vaccine procurement, timely intervention, and monitoring, that can apply directly to rare disease therapies?
Aon Canada Health & Benefits Drug Pricing BulletinAnthony Perlman
A 20 January 2018 joint statement by the pan-Canadian Pharmaceutical Alliance (pCPA) and the Canadian Generic Pharmaceutical Association (CGPA), on behalf of participating federal, provincial, and territorial public drug plans, announced a new five-year initiative that will provide significant drug plan savings to the provinces related to generic drug coverage. Though the primary beneficiary of the savings will be participating public drug plans, the Canadian Life and Health Insurance Association (CLHIA) has confirmed in a public statement that, “these discounts will continue to apply to employer sponsored plans,” thus private drug plan sponsors are likely to see notable financial savings.
The document discusses approaches to drug pricing and access in various countries. It provides details on Health Canada's proposal for expanded international reference pricing, including the criteria for selecting reference countries. The document also examines the impact of international reference pricing on product introduction delays and launch sequencing. It analyzes mechanisms for price setting and reimbursement across different countries. Finally, it touches on reservation prices in negotiations and Germany's multi-stage process for drug reimbursement decisions.
Listeners participated in a live panel session addressing OHIP+, the recently announced expansion of the Ontario drug program to cover young people who are younger than 25 years-old.
This webinar will introduce you to the Patented Medicine Prices Review Board (PMPRB), how they regulate drug pricing in Canada and the proposed changes that will affect cancer patients.
CAPCA wants to make sure that patients have access to innovative and effective cancer treatments, and Heather Logan, ED of CAPCA, will explain how CAPCA is going to do this and answer your questions about the process. This webinar will introduce you to CAPCA and its mandate and to the new pan-Canadian Cancer Drug Funding Sustainability Initiative (DFSI). The goal of DFSI is to ensure that patients continue to have access to innovative and effective cancer treatments, and that the cancer system is achieving maximum value for money invested.
August 19, 2021 from 1-2 pm
CORD’s LAST SUMMER webinar, Part 1 of our series on “How to Get Back to the PMPRB Original Mandate to prevent excessive drug pricing and support pharma R&D investment.” Learn why responding to the most recent (July 15th) proposed guideline changes is very important.
On August 19, 2021 from 1-2 pm, please JOIN:
When: June 10, 2021
Only 5% of rare diseases have an approved drug therapy. Only 60% of orphan medicines approved by the US FDA or EU EMA are approved in Canada, and often many months or years later. Only 34% of approved orphan medicines are funded by Canadian public drug plans. Under the BEST of circumstances, only 10% of eligible patients get access to an approved medicine. And worldwide, only 1% of rare disease patients will receive an approved drug. Most without treatment are children. How can Canada’s Rare Disease Drug Strategy assure all eligible Canadian patients get access to the most appropriate medicine for their individual needs?
Two panels will be tasked to consider a “Canada Leading the Way” strategic pharmaceutic framework that (1) attracts early investment in R&D; (2) reduces and manages risk for early adoption of innovative therapies; and (3) leads to a sustained culture of collaboration and trust among all stakeholders, including regulators, industry, payers, and patients. In particular, what has Canada learned from addressing COVID, for example, in terms of screening, diagnosis, drug repurposing, vaccine procurement, timely intervention, and monitoring, that can apply directly to rare disease therapies?
Aon Canada Health & Benefits Drug Pricing BulletinAnthony Perlman
A 20 January 2018 joint statement by the pan-Canadian Pharmaceutical Alliance (pCPA) and the Canadian Generic Pharmaceutical Association (CGPA), on behalf of participating federal, provincial, and territorial public drug plans, announced a new five-year initiative that will provide significant drug plan savings to the provinces related to generic drug coverage. Though the primary beneficiary of the savings will be participating public drug plans, the Canadian Life and Health Insurance Association (CLHIA) has confirmed in a public statement that, “these discounts will continue to apply to employer sponsored plans,” thus private drug plan sponsors are likely to see notable financial savings.
July 22, 2021 : Aligning on Rare Drug Strategy, PMPRB, and Federal Election
Engage with our Expert Panel in a Townhall style meeting to add your voice on these important issues in preparation for upcoming federal election.
Panelist
Alexandra Chambers (Novartis)
Peter Brenders (BeiGene)
Angela Genge (The Neuro)
Fred Horne (3Sixty Public Affairs)
Leanne Ward (CHEO)
Prescription Medicines Costs in Context April 2022PhRMA
This document discusses the costs of prescription medicines in the United States. It notes that 60 new medicines were approved by the FDA in 2021 for cancer, hemophilia, and COVID treatments. While brand medicine prices declined slightly in 2020, overall medicine spending grew modestly due to rebates and discounts. The majority of medicine spending goes to entities other than the manufacturers, such as insurers, pharmacy benefit managers, and providers. The document argues for reforms that make insurance work better for patients, modernize Medicare drug coverage, protect safety net programs, and end misaligned incentives in the system.
Prescription Medicines - Costs in Context - October 2018PhRMA
This document discusses the costs and context of prescription medicines. It notes that while prescription drug spending is a small percentage of total healthcare costs, certain patients face rising out-of-pocket costs. It also outlines the significant costs and risks of developing new medicines, with the average drug taking over 10 years and $2.6 billion to develop. The document proposes reforms to help lower costs for patients while supporting continued research and development of new treatments.
Prescription Medicines Costs in Context March 2022PhRMA
This document discusses trends in prescription drug costs and spending in the United States. It notes that 60 new medicines were approved by the FDA in 2021 for cancer, hemophilia, and COVID. While brand drug prices declined slightly in 2020, overall drug spending grew modestly. Most drug spending goes to health insurers, pharmacy benefit managers, and other entities rather than drug manufacturers. The majority of drugs dispensed are generics, which provide billions in savings each year. The document argues that while drug spending is projected to increase at a similar rate as overall healthcare costs, patients still face high out-of-pocket costs due to deductibles, coinsurance, and other cost-sharing policies by insurers.
Prescription Medicines Costs in Context November 2019PhRMA
This document discusses the costs and context of prescription medicines. It notes that while prescription drug spending is a small percentage of total healthcare spending, patients often face high out-of-pocket costs. It outlines the significant costs and risks of drug research and development. The document also describes the role of generics in reducing costs over time and how rebates and discounts do not always lower costs for patients.
Prescription Medicines Costs in Context April 2021PhRMA
This document discusses the costs of prescription medicines in the United States. It notes that while brand medicine prices have risen 1.7% in 2019, in line with inflation, many patients still struggle with costs. It also discusses that prescription medicines make up only 14% of total healthcare spending in the US. Finally, it summarizes efforts by PhRMA to make medicines more affordable and accessible for patients.
Prescription Medicines Costs in Context October 2020PhRMA
This document discusses the costs and affordability of prescription medicines in the United States. It notes that while spending on prescription medicines accounts for only 14% of total health care spending, patients face high and rising out-of-pocket costs for medicines. While most medicines sold in the US are generics, brand name medicines face significant price negotiations and rebates paid to insurers and pharmacy benefit managers that often do not lower costs for patients. The document outlines reforms to make medicines more affordable and accessible for patients.
National health accounts - Gerlie Lie, The Global FundOECD Governance
The Global Fund has invested approximately $4.5 million since 2012 to support health accounts through partnerships with WHO and country grants. This funding supports training and capacity building by WHO in shifting over 60 countries to the System of Health Accounts (SHA 2011), allowing distribution of expenditures by disease to be tracked. Over 70 health account exercises have been conducted. Health accounts data help inform grant management, performance indicators, results reporting, replenishment cases, and allocation. Three priority areas are distribution of expenditures by disease, government health expenditures without external resources, and comprehensive pharmaceutical expenditure breakdowns. Examples from Jamaica and Georgia illustrate how this data can be used.
At this webinar, Steve Sampson (Global Public Affairs) discusses how the upcoming federal budget may contain announcements related to the way healthcare is funded in Canada, including changes to the regulation of pharmaceutical prices. Value for taxpayer money should always be the focus for government, but the need for cost-containment needs to be balanced with access to optimal healthcare innovation for patients.
The document summarizes proposed changes to Canada's regulations for pricing patented medicines. It discusses:
- The role of the Patented Medicine Prices Review Board (PMPRB) in regulating drug prices.
- Proposed changes including adding new economic factors, updating comparator countries, and requiring reporting of discounts.
- Potential consequences like reduced drug launches in Canada, delays in drug availability, and price erosion over time.
- Questions around whether the changes will actually lower public drug prices significantly or risk reducing patient access to innovative therapies.
Prescription Medicines Costs in Context January 2020PhRMA
This document discusses the costs and context of prescription medicines. It notes that while prescription drug spending represents 14% of total healthcare spending and a small portion of Medicaid spending, it has enabled breakthrough treatments for chronic diseases. While brand drug prices grew by 0.3% in 2018 after rebates, spending on other healthcare services is projected to grow 5 times faster than prescription drug spending through the next decade. The document also outlines how generics have reduced costs significantly, providing $1.99 trillion in savings over 10 years, and how biosimilars are expected to reduce brand drug sales by $95 billion from 2019-2023 through increased competition.
Webinar 3: (Nov 6 2020). PMPRB: Friend or Foe of Rare Disease Drug Strategy. Webinar 3 in CORD’s Rare Drug Strategy Consultation, a multi-stakeholder panel will consider the potential impact of the PMPRB revised guidelines on entry and access of rare disease therapies, using “real” case examples. Stakeholders will be invited to deliberate on alternatives to the PMPRB guidelines that could better meet the Triple Aim of “timely appropriate patient access”, “optimal, sustainable healthcare expenditure”, and “non-excessive industry compensation that incentivizes launching new therapies and future R&D.”
Presentation:
Kimberly Robinson, Director, Pricing & Market Access, PDCI
Kim Steele, Director, Government and Community Relations, Cystic Fibrosis Canada
Dr. Leanne Ward, Professor, Medical Director of the CHEO Bone Health Clinic, Scientific Director of the Ottawa Pediatric Bone Health Research Group
Fred Horne, Former Alberta Minister of Health and Senior Advisor to 3Sixty Public Affairs
Marissa Poole, Country Lead, Sanofi Canada and General Manager, Sanofi Genzyme Canada
Summer 2020 PMPRB Webinar Series: Webinar 2 (July 16, 2020)
Hearing From Those Who Really Matter. This Webinar will take place after the PMPRB’s promised rescheduled “public forums” and “research webinars.”
Roundtable
Lindy Forte, Principal Consultant, Patient Access Solutions
Dr. Shawn Whatley, family physician, Munk Senior Fellow, Macdonald Laurier Institute and past president of the OMA
Barbara Jaszewski, Advisor Cloud and past global vice president of pricing and market access
Catherine Boivin, SMA Patient
Durhane Wong-Rieger, President & CEO, CORD
Moderator: Bill Dempster, CEO, 3Sixty Public Affairs
Prescription Medicines Costs in Context July 2021PhRMA
This document summarizes information from a report about prescription drug costs and spending in the United States. It notes that 53 new medicines were approved by the FDA in 2020 and discusses trends in drug spending growth rates remaining in line with overall health care spending increases. However, it also outlines challenges patients face in affording medications due to high deductibles, coinsurance, and other out-of-pocket costs not reduced by negotiated rebates and discounts. The report examines spending and policy issues across the entire U.S. health care system that contribute to the complex drug pricing landscape.
This document summarizes a presentation on options for a national pharmacare plan in Canada. It outlines the current fragmented system of drug coverage and past recommendations for reform. It notes that Canadians spend more per capita on prescription drugs than other countries, yet access remains unequal. The presentation argues for a universal, public, evidence-based program with first-dollar coverage to improve health equity and access to treatments while generating savings through bulk purchasing and formulary management.
Webinar 8: Laying A Factual Foundation for Canada’s Rare Drug Program
Feb 12 @ 12 PM ET/ 9 AM PT
Separating Fact from Fiction about rare disease drugs in Canada
Aligning on key issues: Single framework, Innovative access models, and Risk management
Charting the course from Rare Drug Strategy to Rare Drug Program Implementation
Please share this slideshow with anyone who may be interested!
In this webinar:
● What has prompted the recent re-emergence of public calls for national pharmacare?
● What are Canadian health ministers doing to address this issue?
● What are some potential models for national pharmacare that are under discussion?
Contact the presenters:
● Bill Dempster - wdempster@3sixtypublicaffairs.com
● Gerry Jeffcott - gjeffcott@3sixtypublicaffairs.com
View the video: https://youtu.be/Eh3593x4aoI
The document provides an overview of the Canadian pharmaceutical market, highlighting several key trends that will affect pharmaceutical manufacturers. The Canadian market, while smaller than some other countries, still ranks among the top 10 globally in drug spending. Launching a drug in Canada can be profitable if manufacturers understand the specific nuances of the market, such as Canada's complex reimbursement system with both public and private insurance. Health technology assessments play an important role in reimbursement decisions. Manufacturers must tailor their reimbursement and launch strategies to the target payer market, whether public or private plans. Health economic evidence is also becoming increasingly important for market access, pricing, and contracting in Canada.
On June 11, CBO will present preliminary findings of a study of specialty drugs to be released by the agency later this year. The presentation provides information on the prices for specialty drugs, net of rebates and discounts, in Medicare Part D and Medicaid over the 2010–2015 period; the increase in net spending on specialty drugs in each program; and total net spending and out-of-pocket costs for specialty drugs among Medicare Part D enrollees who use such drugs.
Presentation by Anna Anderson-Cook, Jared Maeda, and Lyle Nelson (all of CBO’s Health, Retirement, and Long-Term Analysis Division) at the conference of the American Society of Health Economists.
Canada is the only developed nation without universal prescription drug coverage. Currently, medications are covered through a combination of public, private, and out-of-pocket costs, resulting in inconsistent access across provinces. The Canadian Federation of Medical Students recommends convening a task force to develop a universal national Pharmacare program to ensure all Canadians have equal access to necessary medications. A universal Pharmacare program could save up to $11.4 billion annually by eliminating private insurance inefficiencies and increasing purchasing power for lower drug prices. This would improve health outcomes by increasing medication adherence and protecting Canadians from high out-of-pocket costs.
OHE Lecturing for Professional Training at International Centre of Parliament...Office of Health Economics
On 7th November 2018, Bernarda Zamora delivered a pro bono lecture to professionals from diverse countries enrolled at the Professional Certificate in Strategic Planning organised by the International Centre of Parliamentary Studies.
Author(s) and affiliation(s): Bernarda Zamora, Office of Health Economics
Conference/meeting: Professional Certificate in Strategic Planning organised by the International Centre of Parliamentary Studies
Location: Conference Centre, London
Date: Conference Centre, London
July 22, 2021 : Aligning on Rare Drug Strategy, PMPRB, and Federal Election
Engage with our Expert Panel in a Townhall style meeting to add your voice on these important issues in preparation for upcoming federal election.
Panelist
Alexandra Chambers (Novartis)
Peter Brenders (BeiGene)
Angela Genge (The Neuro)
Fred Horne (3Sixty Public Affairs)
Leanne Ward (CHEO)
Prescription Medicines Costs in Context April 2022PhRMA
This document discusses the costs of prescription medicines in the United States. It notes that 60 new medicines were approved by the FDA in 2021 for cancer, hemophilia, and COVID treatments. While brand medicine prices declined slightly in 2020, overall medicine spending grew modestly due to rebates and discounts. The majority of medicine spending goes to entities other than the manufacturers, such as insurers, pharmacy benefit managers, and providers. The document argues for reforms that make insurance work better for patients, modernize Medicare drug coverage, protect safety net programs, and end misaligned incentives in the system.
Prescription Medicines - Costs in Context - October 2018PhRMA
This document discusses the costs and context of prescription medicines. It notes that while prescription drug spending is a small percentage of total healthcare costs, certain patients face rising out-of-pocket costs. It also outlines the significant costs and risks of developing new medicines, with the average drug taking over 10 years and $2.6 billion to develop. The document proposes reforms to help lower costs for patients while supporting continued research and development of new treatments.
Prescription Medicines Costs in Context March 2022PhRMA
This document discusses trends in prescription drug costs and spending in the United States. It notes that 60 new medicines were approved by the FDA in 2021 for cancer, hemophilia, and COVID. While brand drug prices declined slightly in 2020, overall drug spending grew modestly. Most drug spending goes to health insurers, pharmacy benefit managers, and other entities rather than drug manufacturers. The majority of drugs dispensed are generics, which provide billions in savings each year. The document argues that while drug spending is projected to increase at a similar rate as overall healthcare costs, patients still face high out-of-pocket costs due to deductibles, coinsurance, and other cost-sharing policies by insurers.
Prescription Medicines Costs in Context November 2019PhRMA
This document discusses the costs and context of prescription medicines. It notes that while prescription drug spending is a small percentage of total healthcare spending, patients often face high out-of-pocket costs. It outlines the significant costs and risks of drug research and development. The document also describes the role of generics in reducing costs over time and how rebates and discounts do not always lower costs for patients.
Prescription Medicines Costs in Context April 2021PhRMA
This document discusses the costs of prescription medicines in the United States. It notes that while brand medicine prices have risen 1.7% in 2019, in line with inflation, many patients still struggle with costs. It also discusses that prescription medicines make up only 14% of total healthcare spending in the US. Finally, it summarizes efforts by PhRMA to make medicines more affordable and accessible for patients.
Prescription Medicines Costs in Context October 2020PhRMA
This document discusses the costs and affordability of prescription medicines in the United States. It notes that while spending on prescription medicines accounts for only 14% of total health care spending, patients face high and rising out-of-pocket costs for medicines. While most medicines sold in the US are generics, brand name medicines face significant price negotiations and rebates paid to insurers and pharmacy benefit managers that often do not lower costs for patients. The document outlines reforms to make medicines more affordable and accessible for patients.
National health accounts - Gerlie Lie, The Global FundOECD Governance
The Global Fund has invested approximately $4.5 million since 2012 to support health accounts through partnerships with WHO and country grants. This funding supports training and capacity building by WHO in shifting over 60 countries to the System of Health Accounts (SHA 2011), allowing distribution of expenditures by disease to be tracked. Over 70 health account exercises have been conducted. Health accounts data help inform grant management, performance indicators, results reporting, replenishment cases, and allocation. Three priority areas are distribution of expenditures by disease, government health expenditures without external resources, and comprehensive pharmaceutical expenditure breakdowns. Examples from Jamaica and Georgia illustrate how this data can be used.
At this webinar, Steve Sampson (Global Public Affairs) discusses how the upcoming federal budget may contain announcements related to the way healthcare is funded in Canada, including changes to the regulation of pharmaceutical prices. Value for taxpayer money should always be the focus for government, but the need for cost-containment needs to be balanced with access to optimal healthcare innovation for patients.
The document summarizes proposed changes to Canada's regulations for pricing patented medicines. It discusses:
- The role of the Patented Medicine Prices Review Board (PMPRB) in regulating drug prices.
- Proposed changes including adding new economic factors, updating comparator countries, and requiring reporting of discounts.
- Potential consequences like reduced drug launches in Canada, delays in drug availability, and price erosion over time.
- Questions around whether the changes will actually lower public drug prices significantly or risk reducing patient access to innovative therapies.
Prescription Medicines Costs in Context January 2020PhRMA
This document discusses the costs and context of prescription medicines. It notes that while prescription drug spending represents 14% of total healthcare spending and a small portion of Medicaid spending, it has enabled breakthrough treatments for chronic diseases. While brand drug prices grew by 0.3% in 2018 after rebates, spending on other healthcare services is projected to grow 5 times faster than prescription drug spending through the next decade. The document also outlines how generics have reduced costs significantly, providing $1.99 trillion in savings over 10 years, and how biosimilars are expected to reduce brand drug sales by $95 billion from 2019-2023 through increased competition.
Webinar 3: (Nov 6 2020). PMPRB: Friend or Foe of Rare Disease Drug Strategy. Webinar 3 in CORD’s Rare Drug Strategy Consultation, a multi-stakeholder panel will consider the potential impact of the PMPRB revised guidelines on entry and access of rare disease therapies, using “real” case examples. Stakeholders will be invited to deliberate on alternatives to the PMPRB guidelines that could better meet the Triple Aim of “timely appropriate patient access”, “optimal, sustainable healthcare expenditure”, and “non-excessive industry compensation that incentivizes launching new therapies and future R&D.”
Presentation:
Kimberly Robinson, Director, Pricing & Market Access, PDCI
Kim Steele, Director, Government and Community Relations, Cystic Fibrosis Canada
Dr. Leanne Ward, Professor, Medical Director of the CHEO Bone Health Clinic, Scientific Director of the Ottawa Pediatric Bone Health Research Group
Fred Horne, Former Alberta Minister of Health and Senior Advisor to 3Sixty Public Affairs
Marissa Poole, Country Lead, Sanofi Canada and General Manager, Sanofi Genzyme Canada
Summer 2020 PMPRB Webinar Series: Webinar 2 (July 16, 2020)
Hearing From Those Who Really Matter. This Webinar will take place after the PMPRB’s promised rescheduled “public forums” and “research webinars.”
Roundtable
Lindy Forte, Principal Consultant, Patient Access Solutions
Dr. Shawn Whatley, family physician, Munk Senior Fellow, Macdonald Laurier Institute and past president of the OMA
Barbara Jaszewski, Advisor Cloud and past global vice president of pricing and market access
Catherine Boivin, SMA Patient
Durhane Wong-Rieger, President & CEO, CORD
Moderator: Bill Dempster, CEO, 3Sixty Public Affairs
Prescription Medicines Costs in Context July 2021PhRMA
This document summarizes information from a report about prescription drug costs and spending in the United States. It notes that 53 new medicines were approved by the FDA in 2020 and discusses trends in drug spending growth rates remaining in line with overall health care spending increases. However, it also outlines challenges patients face in affording medications due to high deductibles, coinsurance, and other out-of-pocket costs not reduced by negotiated rebates and discounts. The report examines spending and policy issues across the entire U.S. health care system that contribute to the complex drug pricing landscape.
This document summarizes a presentation on options for a national pharmacare plan in Canada. It outlines the current fragmented system of drug coverage and past recommendations for reform. It notes that Canadians spend more per capita on prescription drugs than other countries, yet access remains unequal. The presentation argues for a universal, public, evidence-based program with first-dollar coverage to improve health equity and access to treatments while generating savings through bulk purchasing and formulary management.
Webinar 8: Laying A Factual Foundation for Canada’s Rare Drug Program
Feb 12 @ 12 PM ET/ 9 AM PT
Separating Fact from Fiction about rare disease drugs in Canada
Aligning on key issues: Single framework, Innovative access models, and Risk management
Charting the course from Rare Drug Strategy to Rare Drug Program Implementation
Please share this slideshow with anyone who may be interested!
In this webinar:
● What has prompted the recent re-emergence of public calls for national pharmacare?
● What are Canadian health ministers doing to address this issue?
● What are some potential models for national pharmacare that are under discussion?
Contact the presenters:
● Bill Dempster - wdempster@3sixtypublicaffairs.com
● Gerry Jeffcott - gjeffcott@3sixtypublicaffairs.com
View the video: https://youtu.be/Eh3593x4aoI
The document provides an overview of the Canadian pharmaceutical market, highlighting several key trends that will affect pharmaceutical manufacturers. The Canadian market, while smaller than some other countries, still ranks among the top 10 globally in drug spending. Launching a drug in Canada can be profitable if manufacturers understand the specific nuances of the market, such as Canada's complex reimbursement system with both public and private insurance. Health technology assessments play an important role in reimbursement decisions. Manufacturers must tailor their reimbursement and launch strategies to the target payer market, whether public or private plans. Health economic evidence is also becoming increasingly important for market access, pricing, and contracting in Canada.
On June 11, CBO will present preliminary findings of a study of specialty drugs to be released by the agency later this year. The presentation provides information on the prices for specialty drugs, net of rebates and discounts, in Medicare Part D and Medicaid over the 2010–2015 period; the increase in net spending on specialty drugs in each program; and total net spending and out-of-pocket costs for specialty drugs among Medicare Part D enrollees who use such drugs.
Presentation by Anna Anderson-Cook, Jared Maeda, and Lyle Nelson (all of CBO’s Health, Retirement, and Long-Term Analysis Division) at the conference of the American Society of Health Economists.
Canada is the only developed nation without universal prescription drug coverage. Currently, medications are covered through a combination of public, private, and out-of-pocket costs, resulting in inconsistent access across provinces. The Canadian Federation of Medical Students recommends convening a task force to develop a universal national Pharmacare program to ensure all Canadians have equal access to necessary medications. A universal Pharmacare program could save up to $11.4 billion annually by eliminating private insurance inefficiencies and increasing purchasing power for lower drug prices. This would improve health outcomes by increasing medication adherence and protecting Canadians from high out-of-pocket costs.
OHE Lecturing for Professional Training at International Centre of Parliament...Office of Health Economics
On 7th November 2018, Bernarda Zamora delivered a pro bono lecture to professionals from diverse countries enrolled at the Professional Certificate in Strategic Planning organised by the International Centre of Parliamentary Studies.
Author(s) and affiliation(s): Bernarda Zamora, Office of Health Economics
Conference/meeting: Professional Certificate in Strategic Planning organised by the International Centre of Parliamentary Studies
Location: Conference Centre, London
Date: Conference Centre, London
This document summarizes a panel discussion on bringing rare disease drugs to Canada. The panel discussed opportunities and challenges, including having the National Pharmacare Council focus on rare disorders, implementing an orphan drug framework, and adopting managed access programs. Panelists represented patients, industry, and government perspectives on issues like national pharmacare and harmonizing provincial formularies. The discussion focused on improving access to treatments for rare diseases in Canada's universal healthcare system.
This presentation discusses innovative pathways to drug access in private drug coverage plans. It notes that many players are involved in private drug plans, including insurers, plan members, plan sponsors, advisors, insurance carriers, pharmacy benefit managers, and pharmacies. It also discusses some of the cost containment measures commonly used by private drug plans, such as generic substitution, tiered formularies, therapeutic substitution, prior authorization, and case management. In closing, it emphasizes getting to know your private drug plan and how plan design can impact access to medications, as well as noting the complexity of coordinating benefits between different plans.
This document discusses workplace wellness programs and their potential to reduce workers' compensation costs by addressing employees' overall health issues. It also provides examples of strategies that have been shown to successfully contain health care costs for public sector employers. Key points include the importance of integrating efforts to manage medical and workers' compensation costs, and examples from Indiana of savings achieved through consumer-driven health plans that encourage preventive care and cost-conscious decision making.
Peter L. Slavin, M.D., 2015 Leadership in Academic Medicine Lectureuabsom
Peter L. Slavin, M.D., president of Massachusetts General Hospital, presented “The Future of Academic Medicine” on Thursday, Aug. 6 as the featured speaker for the 2015 Leadership in Academic Medicine Lecture, sponsored by UAB Medicine.
How to fix the Healthcare Delivery Model around the Globe.pptxpaul young cpa, cga
Blog – How to address issues with the Healthcare Delivery Model – Canada and the World
Healthcare continues to be one of the largest expenses for provinces and territories across Canada - https://nationalpost.com/news/politics/health-care-funding-deadlocked-as-trudeau-says-provinces-wont-get-more-money-without-system-reforms
Healthcare needs to move to homecare model as part of managing beds across the healthcare system - https://www.marketwatch.com/press-release/home-care-services-market-size-in-global-survey-2023-with-risk-analysis-by-company-profiles-forecast-timeframe-2026-2022-12-12
Digital healthcare needs to be embrace by all levels of government as part of managing healthcare including improving outcomes - https://www.mckinsey.com/industries/life-sciences/our-insights/german-e-health-offerings-expand-but-adoption-remains-uneven
Technology continues to evolve with healthcare. More needs to be done to embrace technology as part of improving patient outcomes. https://www.forbes.com/sites/forbesbusinesscouncil/2022/12/09/future-of-health-top-five-digital-health-innovations-for-2023/?sh=21184fab1e5e or https://www.beckershospitalreview.com/innovation/the-top-innovation-trends-of-2022-according-to-health-system-execs.html
Health and wellness programs need to be expanded through tax credits and other policy changes - https://www.shopify.com/ca/enterprise/health-wellness-trends
More needs to be done to address seniors living in poverty including adjusting GIS to a new threshold of 40K - https://www.springfinancial.ca/blog/boost-your-income/guaranteed-income-supplement-gis
More needs to be done with hiring practices of healthcare professional including expanding the nurses, doctors, and other healthcare spots at colleges and universities - https://www.immigration.ca/canadas-lack-of-residencies-for-foreign-trained-doctors-fuelling-healthcare-labour-shortage/
Pharma and drug companies need to work with all levels of government to curb the high costs of drugs - https://www.slideshare.net/secret/iXrYNeBocHT51
Opening spots for more assisted living needs to forge ahead - https://www.slideshare.net/paulyoungcga/policy-analysis-seniors-assisted-living-and-longterm-carepptx
Healthcare needs to look at privatization options as part of managing the delivery healthcare to patients https://www.expatriatehealthcare.com/the-top-10-healthcare-systems-in-the-world-2022/
The United States spends more on healthcare than any other country but has poor health outcomes. Money influences the healthcare system in several ways. The system is fragmented with different providers and payers not sharing information, leading to duplicate tests and costs. A fee-for-service payment model incentivizes providers to see more patients and perform more procedures to increase payments. Lobbying by the pharmaceutical and insurance industries shapes healthcare policies and regulations in ways that prioritize profits over public health. Transforming how care is delivered, such as emphasizing prevention and plant-based diets, could reduce costs and improve health.
This document discusses how employers are changing the healthcare landscape by addressing chronic conditions and improving population health. It notes that chronic conditions drive 86% of healthcare costs and are caused by behaviors like poor diet, smoking, and lack of physical activity. Employer-sponsored primary care clinics and health coaching programs can help improve health outcomes like lowering cholesterol and A1C levels. Engaged patients have lower costs, with actual costs being 1-7% lower than expected. Analysis of three employers found engaged patients saved over $2.6 million compared to non-engaged patients.
MediMeals Investor Presentation - February 2017Cory Glazier
Clinical trials have proven irrevocably that heart disease and diabetes can be reversed through deliberate nutritional therapy with a shift to consuming a whole food, plant-based diet.
MediMeals is an evolutionary health service that makes it as easy for doctors to prescribe scientifically proven meal regimens as it has been to prescribe pharmaceuticals and surgery in the past.
We get nutritionally precise, delicious meals to our patients nationwide, on doctor's orders.
We have reduced the learning curve and time constraints to upgrading diet. Healing the body with food has never been as accessible.
Presentation given by Eric C. Schneider, MD, Senior Vice President for Policy and Research of The Commonwealth Fund at the University of Michigan Institute for Healthcare Policy and Innovation in Ann Arbor, MI on December 7, 2017.
Managing National Health: An Overview of Metrics & OptionsDale Sanders
This is a presentation that I gave at the annual international healthcare conference hosted by the Cayman Islands government. It summarizes the international standards and frameworks for planning and managing the health of a nation. One of the most fun parts of a very fun career was the time that I spent working and living in the Cayman Islands and serving as the CIO of the national health system. The Cayman Islands national health system sat at the intersection of three very influential healthcare ecosystems-- the United States, United Kingdom, and the Pan-American Healthcare Organization. As a result, I was fortunate enough to learn from these international settings and contrast that to the US healthcare system. Other healthcare systems tend to benchmark themselves internationally more so than the United States, where we tend to benchmark ourselves internally. Unfortunately, those internal US benchmarks are the lowest in the developed world by almost every measure of national health.
A new study adds further evidence to suggest that opioid prescribing in the U.S. is skewed and concentrated among a few providers. Researchers looked at prescribing patterns in data from an unspecified national private insurer between 2003-2017.
Around 670,000 providers prescribed more than 8 million standard doses of opioid prescriptions — but more than a quarter of these prescriptions were written by only 1% of physicians. And in 2017, these physicians prescribed nearly half of all the dispensed opioids. This small group of doctors also prescribed higher doses than recommended, and for longer durations than guidelines allow.
What’s encouraging, the authors suggest, is that the vast majority of physicians do seem to follow guidelines. Some caveats: The study was based on one company’s data, and didn’t look at medical reasons behind prescriptions.
The document provides an overview of treatment programs operated by the Ohio Department of Health (ODH) and analyzes how the Affordable Care Act and other changes have impacted these programs. It finds that some programs have seen decreased demand for services while others have increased. It identifies opportunities to better integrate ODH programs into the formal healthcare system to improve care, health outcomes, and lower costs. The report recommends ODH reassess its programs and consider using federal funding more flexibly and creatively to address the state's leading health issues.
The document summarizes the future of America's health care system based on a presentation given to the Ventura Rotary Meeting. It discusses key aspects of health care reform including reducing the uninsured, expanding Medicaid, establishing health insurance exchanges, individual and employer mandates, and revenue generation strategies. Implementation will occur between 2010-2020 with the goals of increasing access to insurance and reducing costs over time. Concerns were raised about the increased costs and bureaucracy that employers and those with current coverage may face during the transition.
The Canadian Hemophilia Society advocated for access to the innovative drug emicizumab (Hemlibra) for Canadians with hemophilia A between 2018-2021. After initial delays, the drug was approved for patients with inhibitors in May 2019 but advocacy continued for broader access. Health technology assessments recommended against funding due to perceived lack of evidence, though patients reported a high disease burden. Advocacy efforts included surveys, letters, media stories, and behind-the-scenes discussions. In August 2021, Quebec partially approved funding while the rest of Canada approved broader public funding in September 2021.
Similar to Roadmap to Optimal Drug Access (Chris Bonnett, H3 Consulting) June 14, 2017 (20)
This document discusses strategies to improve access to drugs for rare diseases in Canada. It proposes establishing Centres of Expertise across the country to provide coordinated rare disease services. It also recommends creating a national rare disease research network and an accelerated drug access pathway. This would involve concurrent regulatory review and managed access programs to provide early access to drugs while collecting additional evidence. The goal is to deliver on the promise of value-based access to rare disease treatments for Canadians.
The document summarizes a webinar on rare diseases held on June 9th, 2023. It discusses the mandate of CORD-RQMO, which is a network of over 100 patient groups that aims to improve the lives of those with rare diseases. It outlines some of the services provided through IRARE, including information sharing and awareness raising. It also discusses challenges with drug access for rare diseases in Canada, including slow reimbursement processes and limited access and treatment for eligible patients. Finally, it announces that the federal government will invest up to $1.5 billion over 3 years in a new Rare Disease Drug Strategy to improve access to drugs and support for patients.
On this webinar, we’ll hear from experts on the issue and invite an open conversation with stakeholders. We need discussion, shared questions and answers and a review of case studies, which is why we are hosting this session.
Panelist:
Neil Palmer, Principal Consultant, WN Palmer & Co. and former PMPRB staff
Michael Dietrich, Executive Director, Policy, Innovative Medicines Canada
Laurene Redding, Global Head, Strategic Pricing (ex-China), BeiGene
Durhane Wong-Rieger, President & CEO, CORD
Moderator: Bill Dempster, CEO, 3Sixty Public Affairs
Rare Disease Drug Access within Rare Disease System
This document discusses challenges with rare disease drug access and proposes frameworks to address barriers. It summarizes an operational description of rare diseases developed by experts that includes a core definition and descriptive framework. The frameworks recognize challenges from a disease's rarity, the need for greater recognition of rare disease burden, and that addressing unmet needs requires coordinated action. The document also outlines health system pathways to treatment access and frameworks for mapping the drug journey and identifying barriers. It proposes three pillars - financing, health services, and governance - for optimal rare disease drug programs.
1) The document outlines Canada's strategy for rare diseases and rare drug access. It discusses the need for improved coordination between patients, healthcare providers, regulators, insurers, and industry.
2) A key focus is on patient engagement and empowerment throughout the process, from diagnosis to treatment to ongoing care. The roles and advocacy of patient groups have changed over time.
3) The strategy proposes several pillars to guide improvement, including increasing access to rare disease treatments consistently across Canada, optimizing evidence collection to inform decisions, supporting optimal patient outcomes and healthcare sustainability, and strengthening alignment between research and innovation systems and access objectives.
This document summarizes a presentation about creating Canada's rare disease network. It discusses barriers to accessing treatments, the role of physician advocacy, and an approach taken in Manitoba and Saskatchewan to build capacity for diagnosing hereditary metabolic disorders. A key part of this approach is the "OMICS First" strategy of starting with comprehensive DNA testing rather than traditional testing. This aims to improve timelines, reduce hospital stays and tests, and lower costs while maintaining quality of care. The presentation also discusses challenges of pricing for rare disease treatments and the need for real-world evidence to be incorporated into decision making.
CORD Rare Drug Conference: June 8-9, 2022
Registries and Real-World Data
INFORM RARE: Beth Potter, Alexandra Wyatt, Pranesh Chakraborty,
Monica Lamoureux, John Adams, Kim Angel
Orion Buske, CEO of Phenotypes, gave a presentation at the CORD Spring Conference in June 2022 about using patient phenotypes to drive genomic diagnostics for rare diseases. He explained that while genome sequencing can diagnose thousands of genetic conditions at once, clinicians need detailed phenotypic information to determine which are relevant to each patient's condition. PhenoTips is a digital platform that uses structured phenotypic data from sources like the Human Phenotype Ontology to help match patients to potential diagnoses, genes, and other related information to support precision medicine. It allows data sharing between hospitals, clinics, and research initiatives to help solve more rare disease cases.
This document summarizes a presentation by Dr. Kym Boycott on clinical genome-wide sequencing. The key points are:
- Genome-wide sequencing (GWS) can diagnose 25-60% of rare genetic diseases, improving patient care and reducing misdiagnoses. However, it requires specialized interpretation and many patients see multiple specialists over 3-6 years before receiving a diagnosis.
- Over 200,000 rare disease patients have been clinically sequenced worldwide. Guidelines developed in Canada recommend GWS for diagnostic evaluation.
- Projects in several Canadian provinces are working to implement clinical GWS, but a national data solution is needed to realize the promise of precision medicine for rare diseases in Canada.
- The proposed
CORD Rare Drug Conference: June 8-9, 2022
Registries and Real-World Data
INFORM RARE: Beth Potter, Alexandra Wyatt, Pranesh Chakraborty,
Monica Lamoureux, John Adams, Kim Angel Opportunities and Challenges for Data Management
CORD Rare Drug Conference June 8-9, 2022
Global, International, and National Rare Disease Networks
Rare Disease Research Network and National Children’s Hospital - Marshall
Summar, Rare Disease Institute
CORD Rare Drug Conference: June 8-9, 2022
Global, International, and National Rare Disease Networks
WHO-RDI Global Rare Disease Network - Matt Bolz-Johnson, EURORDIS
CORD Rare Drug Conference: June 8-9, 2022
Global, International, and National Rare Disease Networks
Canadian Network of Rare Disease Centres of Excellence - Paula Robeson, Children’s Healthcare Canada
Bonescanada.org aims to empower healthcare professionals and patients dealing with childhood-onset rare bone disorders through collaboration, a multidisciplinary team of experts, and overcoming challenges like limited resources, integrating research and care, and facilitating technology and regulatory processes. They have enrolled over 400 children in their research program on conditions like Duchenne muscular dystrophy and osteogenesis imperfecta, using centralized imaging to support international clinical trials. Lessons from research also inform their clinical program and advocacy efforts.
More from Canadian Organization for Rare Disorders (20)
At Malayali Kerala Spa Ajman, Full Service includes individualized care for every client. We specifically design each massage session for the individual needs of the client. Our therapists are always willing to adjust the treatments based on the client's instruction and feedback. This guarantees that every client receives the treatment they expect.
By offering a variety of massage services, our Ajman Spa Massage Center can tackle physical, mental, and emotional illnesses. In addition, efficient identification of specific health conditions and designing treatment plans accordingly can significantly enhance the quality of massaging.
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TEST BANK FOR Health Assessment in Nursing 7th Edition by Weber Chapters 1 - ...rightmanforbloodline
TEST BANK FOR Health Assessment in Nursing 7th Edition by Weber Chapters 1 - 34.
TEST BANK FOR Health Assessment in Nursing 7th Edition by Weber Chapters 1 - 34.
TEST BANK FOR Health Assessment in Nursing 7th Edition by Weber Chapters 1 - 34.
The facial nerve, also known as cranial nerve VII, is one of the 12 cranial nerves originating from the brain. It's a mixed nerve, meaning it contains both sensory and motor fibres, and it plays a crucial role in controlling various facial muscles, as well as conveying sensory information from the taste buds on the anterior two-thirds of the tongue.
End-tidal carbon dioxide (ETCO2) is the level of carbon dioxide that is released at the end of an exhaled breath. ETCO2 levels reflect the adequacy with which carbon dioxide (CO2) is carried in the blood back to the lungs and exhaled.
Non-invasive methods for ETCO2 measurement include capnometry and capnography. Capnometry provides a numerical value for ETCO2. In contrast, capnography delivers a more comprehensive measurement that is displayed in both graphical (waveform) and numerical form.
Sidestream devices can monitor both intubated and non-intubated patients, while mainstream devices are most often limited to intubated patients.
Hypertension and it's role of physiotherapy in it.Vishal kr Thakur
This particular slides consist of- what is hypertension,what are it's causes and it's effect on body, risk factors, symptoms,complications, diagnosis and role of physiotherapy in it.
This slide is very helpful for physiotherapy students and also for other medical and healthcare students.
Here is summary of hypertension -
Hypertension, also known as high blood pressure, is a serious medical condition that occurs when blood pressure in the body's arteries is consistently too high. Blood pressure is the force of blood pushing against the walls of blood vessels as the heart pumps it. Hypertension can increase the risk of heart disease, brain disease, kidney disease, and premature death.
Michigan HealthTech Market Map 2024. Includes 7 categories: Policy Makers, Academic Innovation Centers, Digital Health Providers, Healthcare Providers, Payers / Insurance, Device Companies, Life Science Companies, Innovation Accelerators. Developed by the Michigan-Israel Business Accelerator
R3 Stem Cell Therapy: A New Hope for Women with Ovarian FailureR3 Stem Cell
Discover the groundbreaking advancements in stem cell therapy by R3 Stem Cell, offering new hope for women with ovarian failure. This innovative treatment aims to restore ovarian function, improve fertility, and enhance overall well-being, revolutionizing reproductive health for women worldwide.
VEDANTA AIR AMBULANCE SERVICES IN REWA AT A COST-EFFECTIVE PRICE.pdfVedanta A
Air Ambulance Services In Rewa works in close coordination with ground-based emergency services, including local Emergency Medical Services, fire departments, and law enforcement agencies.
More@: https://tinyurl.com/2shrryhx
More@: https://tinyurl.com/5n8h3wp8
English Drug and Alcohol Commissioners June 2024.pptxMatSouthwell1
Presentation made by Mat Southwell to the Harm Reduction Working Group of the English Drug and Alcohol Commissioners. Discuss stimulants, OAMT, NSP coverage and community-led approach to DCRs. Focussing on active drug user perspectives and interests
CHAPTER 1 SEMESTER V COMMUNICATION TECHNIQUES FOR CHILDREN.pdfSachin Sharma
Here are some key objectives of communication with children:
Build Trust and Security:
Establish a safe and supportive environment where children feel comfortable expressing themselves.
Encourage Expression:
Enable children to articulate their thoughts, feelings, and experiences.
Promote Emotional Understanding:
Help children identify and understand their own emotions and the emotions of others.
Enhance Listening Skills:
Develop children’s ability to listen attentively and respond appropriately.
Foster Positive Relationships:
Strengthen the bond between children and caregivers, peers, and other adults.
Support Learning and Development:
Aid cognitive and language development through engaging and meaningful conversations.
Teach Social Skills:
Encourage polite, respectful, and empathetic interactions with others.
Resolve Conflicts:
Provide tools and guidance for children to handle disagreements constructively.
Encourage Independence:
Support children in making decisions and solving problems on their own.
Provide Reassurance and Comfort:
Offer comfort and understanding during times of distress or uncertainty.
Reinforce Positive Behavior:
Acknowledge and encourage positive actions and behaviors.
Guide and Educate:
Offer clear instructions and explanations to help children understand expectations and learn new concepts.
By focusing on these objectives, communication with children can be both effective and nurturing, supporting their overall growth and well-being.
CHAPTER 1 SEMESTER V COMMUNICATION TECHNIQUES FOR CHILDREN.pdf
Roadmap to Optimal Drug Access (Chris Bonnett, H3 Consulting) June 14, 2017
1. How do Ontario children and young
adults access prescription drugs?
Chris Bonnett, MHSc, PhD (Cand.)
H3 Consulting / hthree.ca
CORD / Toronto / June 14, 2017
2. In ten minutes…
1. Special drug coverage for children and young adults across Canada
2. Estimates of coverage in Ontario: provincial and private drug plans
3. Potential therapeutic classes relevant to children and young adults
4. Considerations and questions
5. Paying for drugs: OHIP+ conclusions
3. Provincial Special Drug Coverage
Children and Young Adults
Prov Special
Drug
Programs Eligibility
Notes
BC None
AB Child
Health
Benefit Low
income
(<
$26,023,
+);
<
age
19/21
SK Children’s
Drug
Plan,
Insulin
Pump
(IP)
CDP:
$25 per
drug;
<
age
15.
IP:
<
age
26.
MB Insulin
Pump <
age
18.
ON OHIP+
(proposed) Universal
<
age
25;
ODB+EAP
drugs;
no
cost
QC None
NB Growth
Hormone
Deficiency
(GHD) <
age
19;
20%
up
to
$20/drug,
up
to
$500/family/yr.
NS Insulin
Pump <
age
25
PEI GHD;
Immunization; IP GHD,
Imm:
<
age
18.
IP:
<
age
19.
NL Select
Needs
Plan;
IP SN:
GHD
up
to
18.
IP:
<
age
25.
Sources: (1) Clement FM, et al., 2016. Canadian Publicly Funded Prescription Drug Plans, Expenditures and an Overview of
Patient Impacts. University of Calgary, School of Public Policy. https://obrieniph.ucalgary.ca/system/files/comparison-‐of-‐
canadian-‐publicly-‐funded-‐drug-‐plans-‐for-‐alberta-‐health-‐feb-‐1-‐2016.pdf. (2) Provincial government websites.
4. Public: Unclear
Government
drug
spending
(2014,
ages
0
– 24):
$146,005,000
1
Incremental provincial
drug
spending:
$319,000,000
Proposed
annual
drug
spending
(2018): $465,000,000
2
Total
ON
Beneficiaries
(ages
0
– 24): 3,914,000
3
Percent
of
total
population
(13,448,000): 29
3
Per
capita
(ages
0
– 24): $119
(2018,
implied)
OPDP
Coverage
Estimates
4
ODB
Programs 3.94
mm
(28%)
• Beneficiaries
(ages
0
– 19) 400,000
eligible
• Beneficiaries
(ages
0
– 24) 244,000
(60%)
claim
Other
public 0.24
mm
(2%)
Private
insurers
7.74
mm
(55%)
Uninsured 2.24
mm
(16%)
Total 14.16
mm
(105%
of
population)
Sources: (1) CIHI NHEX 1975-‐2016 Open Data. (2) Ontario government News Release, May 23, 2017. (3) Statistics Canada,
2016 Census. (4) 2015/16 Report Card for the Ontario Drug Benefit Program. Private insurance coverage is unreliable.
5. Private: We know even less
• Typical private drug plan prescription drug coverage is for children to
age 18, except age 23 or 25 if a full time student, or if physically or
mentally incapable of self-‐support. 1
• Most plans reimburse 100%, 80% or 90% of a much broad(er) formulary,2
though few have limits on out-‐of-‐pocket spending.
• Current private drug spending for ages 0 to 24: unknown.
• Telus Health, ages 0 – 29: 3
• 30.7% of claimants account for 12.4% of total eligible costs.
• OHIP+ may save 8% to 11% of drug claims, defer other cost controls. 4
Notes: (1) There are over 100,000 private health plans, and many variations on eligibility for both members and drugs.
(2) PDCI Market Access reported that their database of private drug plans reimbursed 3,300 more DINs than the ODB
formulary. See Pharmacare Costing in Canada, March 2016, p.21. (3) Telus Health, 2016 Data Trends. (4) M. Sullivan,
Cubic Health, LinkedIn blog May 1, 2017; F. Naranjo, Collins Barrow, quoted in Cdn HR Reporter, May 23, 2017
6. Top 10 Therapeutic Classes
Children and Young Adults
Class
Rank
/
Name
Avg.
Cost
$
per
script
Notes
2 Diabetes 80 Metformin
only
generic
in
top
10;
14%
trend
4 Depression 41 Higher
use
offset
by
lower
cost
generics
5 Asthma 73 Most
products
brand
only;
generic
fill
35%
6 Infections 33 Rank
3rd in
utilization;
-‐8%
trend
9 Cancer 503 Biggest
pipeline;
12%
trend
10 ADHD 96 Mostly
generic,
but
14%
trend
11 Multiple
sclerosis 1,847 Most
often
diagnosed
in
young adults
41 Rare
diseases 4,686 Few
products
currently,
but
42% trend
48 Cystic
fibrosis 3,216 Orkambi®
could
benefit
50%
@
$260,000/yr
Source: Express Scripts Canada, 2016 Drug Trend Report. http://www.express-‐scripts.ca/knowledge-‐centre/drug-‐trend-‐
reports. Rank is by annual claim cost.
7. Considerations and Questions
General
1. Who are “most in need and least able to pay”? 1
2. No detail / certainty on estimated cost. What assumptions?
3. Will impacts (intended and not) of new drug coverage be measured?
Private Drug Plans
1. Insured plans will not see immediate cost reductions; ASO will. 2
2. Young plan members are usually low cost; rates may increase for others.
3. Will some employers exclude members under age 25, even though the
OPDP formulary provides less extensive coverage?
4. Unknown future costs: Could Employer Health Tax be increased? 3
Notes: (1) 2017 Ontario Budget. http://www.fin.gov.on.ca/en/budget/ontariobudgets/2017/. (2) Insured plans (pooled or
experience-‐rated) are typical for smaller employers (<50 to 100 employees). ASO (Administrative Services Only) plans
are self-‐insured by larger employers. (3) 2017 Budget (Table 6.14) estimates EHT revenue at $5.9 billion for 2016-‐17.
8. OHIP+ Conclusions
1. OHIP+ coverage is unique in Canada. Other provinces have specific
targets: low income families or certain diagnoses. Some have co-‐pays.
Quebec offers consolidated, consistent universal coverage model.
2. Budget speaks of those in need, but message then changes to equity
and supporting notion of universal pharmacare. Immediate purpose
and longer-‐term goals are unclear.
3. Quick implementation means consultation may be welcomed…or
discouraged so that Ministry can meet its deadline…but something
will have to be implemented before the 2018 election.
4. A welcome surprise to employers. Biggest impact will be on ASO plans
with large, recurring claims…but smaller employers could choose to
eliminate all coverage for Ontario plan members under age 25.