1.28.2009

More Velcade-Style Risk-Sharing in the UK?


via the IN VIVO Blog by Melanie Senior on 21/01/09

It appears that Janssen-Cilag feels a lot better now about its pay-for-performance scheme around multiple myeloma drug bortezemib (Velcade) than it did when the program was introduced in 2007.
The Velcade Response Scheme (VRS) came about out of desperation: cost-effectiveness watchdog NICE had turned down the drug as too expensive, so Janssen-Cilag, to its credit, said to the UK’s state payer, the Department of Health, ok, well if we promise to charge only when the drug is effective (and refund you if not), then will you give this to patients? The answer was yes. And now, not only have all of the UK’s Primary Care Trusts have signed up to the VRS, according to a Janssen spokesperson, but this scheme “may now be a good example of how a performance-based scheme could be structured.” That’s not a statement from Janssen; it’s from a position document issued last year by the British Oncology Pharmacy Association on risk-sharing schemes.
Indeed, such schemes have, perhaps inevitably, become a rather more regular feature of the UK drug landscape—making Janssen feel more pioneering than desperate (though Janssen isn’t the first to guarantee performance; Pfizer tried with Lipitor too).

Most of the other recent flavors of risk-sharing programs around expensive cancer drugs emerged, like VRS did, as a result of a negative NICE appraisal. Merck-Serono offered the Cetuximab Cost-Share Program around Erbitux in metastatic colorectal cancer, which involved refunding primary care trusts the cost of any vials of the drug used for patients that fell into a pre-agreed ‘non-responder’ category at up to 6 weeks. Roche instigated the ‘Tarceva Access Program’ for its NSCLC drug erlotinib, offering a rebate, in the form of a credit note against any future Roche purchase, for the amount that the drug cost over and above the cost of the incumbent NSCLC treatment docetaxel (Sanofi-Aventis' Taxotere) for an average patient duration (with an upper limit on the total number of packs).

Now granted, Roche’s program was initially introduced as a means to claw market share off docetaxel, which it was struggling to do ahead of NICE guidance. But when NICE found Tarceva to be un-cost effective—with questions around the lack of comparative data with docetaxel in particular--the scheme was formally proposed to NICE as part of a re-review. In November 2008, NICE issued positive guidance—but only on condition that the overall treatment cost remained in line with that of docetaxel. Roche had to drop the price by about 7.5%.

Critics say such programs are simply a way for industry to coerce NICE into a ‘yes’. Maybe. But there’s no denying that such schemes represent a logical way to improve patient access without breaking the bank. Indeed, the new UK drug pricing contract, the PPRS, formalizes a bunch of patient access schemes, including risk-sharing programs. And NICE, as we heard from CEO Andrew Dillon last week, would prefer such schemes to be proposed up front, before a drug is submitted for review, rather than as a last-resort of the drug fails the cost-test.

Small wonder, then, that in the last three or four months since the PPRS was published, the department of health has been in contact with various companies about schemes around several “high profile” drugs, according to David Thomson, Lead Pharmacist at the Yorkshire Cancer Network and author of the BOPA position statement.

The big problem is administration. As it is, it’s complex to administer rebates and track outcomes. The more different schemes are available, the harder that becomes. “Anecdotal evidence suggests that the VRS [and a similar scheme around Sutent] aren’t necessarily bringing the expected levels of financial benefit to the National Health Service,” Thomson told The IN VIVO Blog.

Add to this the problem of patchy uptake or availability of some of the existing handful of programs across the country, and the possibility of multiple risk-programs across a single drug for different indications, and it’s easy to see why BOPA's pushing for some sort of risk-sharing plan template....and why we may not, after all, see a flood of VRS-followers soon.

image by flickr user fboosman used under a creative commons license

© Copyright 2008 Windhover Information Inc. www.windhover.com/blog

NICE to put QALY under examination

LONDON, Jan 27 (APM) - NICE on Tuesday announced an arms-length investigation into how it values health technology, potentially putting the quality-adjusted life year (QALY) under the microscope.
In a press release, the cost-effectiveness body said NICE chairman, Professor Mike Rawlins, has written to England's top health minister announcing a "short study of how value is taken into account when looking at new health technologies". The study will involve submissions and the use of a series of workshops involving the healthcare industries, patients and the wider public, together with representatives of the NHS to explore this issue, NICE said.
NICE also said the Professor of health law, ethics and policy at University College London, Ian Kennedy has agreed to lead the study. Quoted in the release, Rawlins said: "This study which will look at whether particular forms of value are more important than others; and will explore factors that should be taken into account in establishing the value of new health technologies."

QALY

No particular mention of the QALY was made in the release but the measure is at the centre of NICE's work and has been doggedly defended by the institute despite increasing hostility from industry. However, a shift may have taken place with the new UK pricing contract which outlined a greater role for NICE, bringing it to the centre of UK drug pricing.

The pharma industry is known to have pressed for a much wider examination of the benefits of medicines including keeping people in work, reducing the workload of carers and saving the National Health Service costs in reduced hospital admissions.
Rawlins noted a recent report on the future of the biotechnology industry stressed the importance of NICE and the pharmaceutical industry working towards a shared understanding of how to value innovative new health technologies, adding, "NICE supports that view."

ns/ak

nick.smith@apmnews.com
[14027] 27/01/2009 11:02 GMT - INDUSTRY

1.27.2009

Wales sidesteps NICE recommendation on kidney cancer drug access

Scrip

Welsh patients will be able to receive four kidney cancer drugs that have not been
recommended by the National Institute for health and Clinical Excellence (NICE), the
Welsh health minister Edwina Hart has announced.
The decision will allow greater access to four drugs currently being reviewed by NICE
for advanced renal cancer - Pfizer's Sutent (sunitinib), Genentech's Avastin
(bevacizumab), Bayer's Nexavar (sorafenib) and Wyeth's Torisel (temsirolimus). None
of the drugs was found cost-effective a draft NICE appraisal last August; the assessment
of the treatments has since been extended, with final guidance expected this month
(Scrip Online, October 21st, 2008). However, the health minister has instructed Local Health Boards (LHBs) to provide the drugs to end-of-life patients with kidney cancer, with immediate effect, choosing not to wait for NICE's decision. Although describing the move as a "temporary arrangement", the health minister added it was "unacceptable" for patients to be kept waiting for the treatments.
The decision follows a clinical audit of Sutent issued last December. Originally, NICE
and the All Wales Medicines Strategy Group (AWMSG) issued guidance that the drug
should not be funded by the NHS as it was too expensive (Scrip Online, August 8th,
2008), thus leaving funding decisions to LHBs for individual patients. However, a study undertaken by the Medical Director of NHS Wales Professor Mike Harmer found that of 73 requests for Sutent only 23 received the treatment in 2008, raising questions of consistency; the report revealed that all patients who were recommended the treatment in Neath, Port Talbot and Bridgend received it, while only one of 13 patients received the drug in Cardiff and none of the 14 patients recommended received the drug in Swansea.
The health minister has already shown she is prepared for Wales to make its own
decisions regarding drug availability; in July last year she made Novartis's Lucentis
(ranibizumab) for wet age-related macular degeneration (AMD) in both eyes available
on the Welsh NHS, a month before final guidance for England and Wales was confirmed
by NICE (Scrip Online, July 17th 2008 and August 27th, 2008).
NICE has proposed changing its cost-effectiveness parameters for end-of-life drugs,
partly in response to a public outcry over the initial draft of its assessment of the four
kidney anticancers.

SCRIP - World Pharmaceutical News - www.scrippharma.com
FILED 26 January 2009 COPYRIGHT Informa UK Ltd 2009
PHIND: Pharma & Healthcare Ind News - today only (PHID)

1.20.2009

‘Comparator Report on Patient Access to Cancer Drugs in Europe’ reveals significant inequalities still remain

Brussels, 16th January 2009 – European patients still face unequal access to cancer treatment, depending on where they live. This was confirmed in a report published today by Dr Nils Wilking, clinical oncologist at the Karolinska Institutet in Stockholm, Sweden, and Prof Bengt Jönsson, Professor of Health Economics at the Stockholm School of Economics. These inequalities and gaps in survival of cancer patients are particularly noticeable when comparing Eastern Europe with Northern and Western Europe.

The report, based on findings from the 27 EU Member States (excluding Cyprus and Malta), Iceland, Norway and Switzerland, updates and improves on two earlier reports by the same authors in 2005 and 2007. This most recent report was supported by an unrestricted grant from EFPIA, the Federation of the research-based pharmaceutical industry in Europe. Analyses were conducted by i3 Innovus, a company specializing in health economics and outcomes research. “Appropriate access to new treatments is vital, and examining variations in patient access between countries is a positive way to stimulate discussions on the optimal use of new technologies and treatment,” said Brian Ager, Director General of EFPIA.

The report reveals that whereas cancer incidence is increasing, cancer mortality is decreasing, indicating the positive impact of screening programmes and improvements in treatments. “New treatments have made it possible to target diseases more effectively. For cancer patients, these newer therapies mean an improved quality of life, with less time spent in hospital and the chance to return to their day-to-day activities earlier”, said Dr Wilking.

However the report highlights wide gaps in Europe in relative survival rates. For example, in Sweden 60.3 % of men and 61.7 % of women diagnosed with cancer survive compared to only 37.7 % of men and 49.3 % of women in the Czech Republic. EUROCARE 4 data also shows that for a similar incidence, cancer patients in Sweden have greater chances of survival than those in the UK. Healthcare systems in Europe are spending more on cancer, but this expenditure remains lower than the relative burden of cancer in comparison to other diseases.

Patients in Austria, France and Switzerland have the broadest access to newer cancer treatments while Poland, the Czech Republic and the UK continue to lag behind. Prof Jönsson emphasized “The inequalities –highlighted in our original report in 2005 – still remain. For patients and society this is a real concern, as expectations are that all patients in Europe should have equal opportunity to access these treatments, particularly when evidence shows that access to cancer treatment is linked to an improvement in outcome”.

The report authors urged policy-makers to take action - 1.2 million deaths were caused by cancer in Europe in 2006 - and proposed new policies to improve treatment access for patients in Europe:

- Adapt healthcare budgets generally and hospital budgets specifically to incorporate the introduction of new cancer drugs;
- Introduce separate funding for cancer drugs, with or without requirements of an additional gathering of data;
- Expedite (regulatory and economic) review times for innovative cancer drugs
- Promote a European collaborative approach to collecting available scientific information for Health Technology Assessment (HTA)

The report is available for download on www.comparatorreports.se

1.13.2009

Oncology Market Access Conference, April 22nd-23rd Zurich

eyeforpharma hosts the 2009 Oncology Market Access conference on 22nd-23rd April in Zurich. I have been told by the organizer that the conference is looking to be very popular. The website and brochure for the conference have been updated, please take a look.

New rules on drugs will not increase access for terminally ill: expert


New rules issued by the NHS drugs rationing body to increase access to drugs for terminally ill people will not work, an expert has said.
 
by Rebecca Smith, Medical Editor, Telegraph

The National Institute for health and Clinical Excellence (Nice) has told its drugs appraisals committees to be more flexible and approve drugs that would not normally be considered cost effective because they are expensive and only extend life by a short period.
The new rules were praised by charities and patient groups who felt that, for some patients with rare terminal illnesses, it could mean they would get drugs that would otherwise be denied them.
But James Raftery, Professor of Health Technology Assessment at Southampton University, says that the new arrangements will do little to improve availability of expensive drugs and may result in other patient groups being denied treatment.
Writing in the British Medical Journal online he said during 1999-2008, NICE rejected 11 drugs on the grounds of cost effectiveness.
The new advice applies to treatments that affect small numbers of patients who are not expected to live more than 24 months, and that offer demonstrable survival benefits, at least an extra three months of life, compared with current NHS practice.
Professor Raftery examined the effect the new arrangements would have had on all cancer drugs that NICE has refused or proposed to refuse because of cost effectiveness.
He found that few of the rejected drugs would qualify under the new criteria, with most failing to meet the criterion that no alternative treatment with comparable benefits existed.
He also warns that making an exception for any group sets a precedent for other groups, and that allowing more expensive treatments for a small group of patients within a fixed overall budget would result in other patient groups being denied treatment.
Prof Raftery said: "My analysis suggests that NICE's new arrangements for appraising end of life drugs may do little to improve availability of expensive cancer treatments. Few of the rejected drugs would qualify under the new criteria, with much depending on the interpretation of the criterion that no alternative treatment with comparable benefit is available through the NHS.
"NICE will celebrate its 10th birthday in 2009 having had to make a major change in its methods. Its attempt to minimise the effects of these changes will no doubt be tested in future appeals against its findings."
A spokesman for Nice said: "The supplementary advice we are now providing our Independent Committees with enables them to explore the perception that society may place greater value on extensions to life in circumstances where life expectancy is shortened. We think it likely that some treatments will be recommended where in the past they might not. We can't predict which ones will be or how many, perhaps no more than a one or two a year, but it depends to a great extent of what treatments get licensed in the future.
"We recognise that the supplementary advice is controversial and acknowledge there could be concerns that other, equally deserving, patient groups could lose out. We will therefore be ensuring an evaluation is undertaken to investigate whether the scheme is achieving its intended purpose."

1.12.2009

France to increase cost benefit assessments of new medicines


France's HAS three-year plan includes economic assessment

Scrip

France's HAS, an agency set up three years ago to advise the government on healthcare
issues, has set out a three-year work programme for 2009-11 that emphasises its dual
economic and scientific roles. The agency was reorganised last year and set up a new medico-economic committee that is charged with devising rational reimbursement policies and otherwise guiding public spending on healthcare. HAS's aim is to have systems in place by 2011 that will provide a functioning, interdisciplinary evaluation service for the government and healthcare professionals.
Until now, the agency has limited its assessments to the medical benefits of different treatments, but its 2009-11 strategy puts the cost of treatments into the equation. It expects to conduct more postmarketing studies and to develop methods for comparing the relative effectiveness of different products and practices.
The government criticised the agency last year for working too slowly. It was struggling to cut costs from the national healthcare budget and was looking to the HAS for costeffectiveness guidance on several classes of drugs. Perhaps stung by this public rebuke,the agency has set a 2011 target of completing its evaluation of newly licensed drugs within 90 days, and a 12-month timeframe for any re-evaluation of an entire class of drugs, which might be extended to 18 months for particularly complex assessments.
The HAS also plans to examine how to set up a short-response procedure and to
determine the circumstances in which an accelerated assessment might be appropriate.
Improving the quality of the information given to healthcare professionals is also among the agency's objectives for the next three years. It notes that its responsibility to inform patients and prescribers about medicines is duplicated by Afssaps, the medicines regulator, and it hopes that the two agencies can work together. Both agencies publish guidance on the use of medicines.
The HAS is also looking at the way the industry communicates with doctors and it plans to publish a report later this year on the way doctors perceive the information they get from sales reps. It plans to establish best-practice guidance for pharmaceutical companies, but here again it recognises that this effort might overlap the responsibilities of other agencies.
Besides working more closely with French organisations, the HAS says that it will coordinate its efforts with similar agencies in other countries, including NICE in the UK, Germany's IQWIG, the Danish National Board of Health and the Health Quality Authority in Ireland. It plans to deepen its participation in the European
Network for Health Technology Assessment and the European Network for Patient
Safety.

SCRIP - World Pharmaceutical News - www.scrippharma.com FILED 09
January 2009 COPYRIGHT Informa UK Ltd 2009

1.06.2009

Opportunities @ Double Helix Consulting

Hello everyone & happy 2009! Interested candidates please see contact details below.
best wishes
Ulf

Title: Consultant—Biopharmaceutical Market Access

Summary: Double Helix Consulting US (DHC US) is the newly formed US-based life sciences consulting division of London-based Double Helix Development group which has provided market research and market access consulting services to the biopharmaceutical and medical device industries for nearly 15 years. We seek a highly motivated entrepreneurial executive with experience and expertise in the area of market access, including pricing and reimbursement, to help build an exciting and dynamic consulting organization with offices in the greater NYC metro area. The ideal candidate will be able to leverage existing and foster new relationships with leading biopharma companies and win business in a highly competitive market. The Consultant will collaborate closely with DHC US senior management to (a) define service and solution offerings, (b) market and secure consulting engagements with target clients, and (c) manage project teams to complete consulting assignments on time and on budget. Compensation commensurate with experience. Generous benefits available. DHC US is an equal opportunity employer that celebrates diversity at all levels of our organization. EOE/M/F/D/V

Responsibilities:
The Consultant will work with clients and DHC US colleagues to:
• Evaluate reimbursement environment and design strategies to enhance technology adoption and coverage policies among payers, HTA and quality assurance groups (e.g., AHRQ, NCQA, JCAHO), professional societies, and other stakeholders
• Contribute to establishing and maintaining a Market Access Advisory Network including health economists, clinical opinions leaders, patient groups and policy makers
• Develop market building and expansion strategies, including programs to educate customers regarding product value
• Evaluate target product profiles and commercialization scenarios to guide clinical program and trial design, including choice of target populations, duration, comparators and endpoints
• Integrate clinical, market, and payer data to prepare HTAs and product dossier in formats defined by payers and industry associations, e.g., AMCP, WellPoint
• Develop programs/materials for use by field staff that integrate information on product value to support strategies for optimizing revenues, reimbursement, and formulary positioning across all managed markets

Education and Experience:
• MD or PharmD; or Masters or PhD/ScD in a quantitative, health-related field—health services research, economics, epidemiology, statistics or business
• Minimum 8 years’ client- and/or consultant-side biopharmaceutical industry experience, including substantial experience supporting Phase III, peri-launch and launch strategy
• Experience working with payers and decision-makers on evidence-based customer strategies
• Experience demonstrating product value, including preparing AMCP dossiers and/or submissions to HTA agencies
• Experience making substantial contributions to commercial assessment, licensing & development, portfolio management, lifecycle planning, M&A evaluation and/or alliance management desirable

Other Qualifications:
• Proven track record of excellence in written and oral communication of complex technical information
• Strong collaborative style and persuasion skills to build consensus, effectively manage project teams, and achieve objectives
• Ability and willingness to travel up to 40%, primarily domestic

Contact Information: Interested candidates should forward resume and cover note to hr@dhelixc.com

12.19.2008

New short course - economic evaluation for health technology - Brazil

Location: Porto Alegre , Rio Grande do Sul, Brazil
Dates: 13-14 January 2009
Venue: University of Rio Grande do Sul (Universidade Federal do Rio Grande do Sul)
Course Organizers: Prof. Dr. Marcia Regina Godoy, Prof. Dr. Giacomo Balbinotto Neto, Prof. Dr. Ricardo Letizia Garcia
Language: Portuguese

Intended Audience:

Anyone undertaking or managing of health technology assessment, including in the context of cost-effectiveness analysis

The University of Rio Grande do Sul (UFRGS) is pleased to announce the short course "Economic Evaluation for Health Tecnology".

The short course will provide:

Background information on the theoretical basis for, & application of economic evaluation for health technology
a practical guide to data input, data analysis, and the interpretation of studies of health tecnology assessment (HTA) and economic evaluation for health tecnology
An overview of methodological issues and recent developments in the application of HTA

This short course will provide an opportunity for those interested in the application of HTA to discuss both practical and theoretical issues raised when applying the method. The short course will include group work sessions with feedback. No knowledge of economics or HTA is assumed

Contact us
If you would like to be considered for enrolment or would like to ask any questions regarding this short course, please send your e-mail to Claudia Gomes - claug@ufrgs.br

Home page: http://www.ppge.ufrgs.br/ats/minicurso.php

12.16.2008

Health Economics, what's up in 2009?

Dear Readers,

Just looking at the news of Pfizer, Elan and other Pharma’s laying off a lot of people reminds my to squeeze in a reflection post towards the end of the year. This has truly not been an easy last quarter with financial crises kicking in big time and stock market tumbling, an unpleasant event for all of us with varying degrees of intensity.. ;(
But what does this all mean for pharma and the health economics, pricing & reimbursement fraction like ourselves? The layoffs as we know are due to some well known reasons but its also true that cash strapped governments – with all rescue efforts for banks and automotive companies, the scope is truly amazing to every liberal economist – will start, and have done so already, eyeing at drug prices once more again in order to cut the healthcare bill. The good news of the financial disaster is one finally feels like a customer again when stepping close to bank counter... incredible what is possible if they truly need your money… anyway back to the topic: Many mandatory price reductions are underway or being announced in various countries, especially Eastern Europe. This clearly means for 2009 more challenges for the health economists and pricing folks but where is this all going? Some of my friends are not convinced that health economics has a too bright future in its current application (e.g. developing models for dossiers and haggling until thresholds are met - than its mostly too late) given the shift towards personalized medicines for limited populations where static cost-effectiveness criteria, such as the 30.000 pounds applied by NICE, will never be met anyhow – so why bother developing those expensive economic models in the first place? Indeed it seems that certain commercial arrangements etc. are more successful going foreward than focusing too much on the model details. I guess health economics must be shifting much more towards aiding internal commercial decision making such as licensing/development (with the pipelines drying up of outmost importance when going on the biotech shopping tour) but moreover overall pricing strategy. That is something very much discussed for a long time but in the end still not very well done in many circumstances, at least as I have been told. Decisions about product development and initial pricing have serious consequences at launch these days and therefore early models will become more crucial in “crash testing” commercial viability with payors - of course that brings us back to the threshold problem unless more flexibility is build into the sytem (in that regard I recommend to read a recent post from HTA blog “The QALY must change” http://www.htablog.com/2008/12/qaly-must-change-says-industry.html).
The latest announcements in the UK in order to reform the PPRS (a company will still set the initial launch price for its new product and will be able to increase or decrease this price, as further evidence or new indications change the value that the medicine provides to patients, but only after NICE has conducted an appraisal to determine whether the revised price provides value) certainly point towards that direction. I am curious to hear as to how you see things evolving?
Anyhow it will remain entertaining and surely will we be very busy again in 2009. Until than Merry Christmas, Happy New Year and relaxing holidays to everyone!
Cheers
Ulf

12.03.2008

British Balance Gain Versus Cost of Latest Drugs

By GARDINER HARRIS
The New York Times

RUISLIP, England — When Bruce Hardy’s kidney cancer spread to his lung, his doctor recommended an expensive new pill from Pfizer. But Mr. Hardy is British, and the British health authorities refused to buy the medicine. His wife has been distraught.
“Everybody should be allowed to have as much life as they can,” Joy Hardy said in the couple’s modest home outside London.
If the Hardys lived in the United States or just about any European country other than Britain, Mr. Hardy would most likely get the drug, although he might have to pay part of the cost. A clinical trial showed that the pill, called Sutent, delays cancer progression for six months at an estimated treatment cost of $54,000.
But at that price, Mr. Hardy’s life is not worth prolonging, according to a British government agency, the National Institute for Health and Clinical Excellence. The institute, known as NICE, has decided that Britain, except in rare cases, can afford only £15,000, or about $22,750, to save six months of a citizen’s life.
British authorities, after a storm of protest, are reconsidering their decision on the cancer drug and others.
For years, Britain was almost alone in using evidence of cost-effectiveness to decide what to pay for. But skyrocketing prices for drugs and medical devices have led a growing number of countries to ask the hardest of questions: How much is life worth? For many, NICE has the answer.
Top health officials in Austria, Brazil, Colombia and Thailand said in interviews that NICE now strongly influences their policies.
“All the middle-income countries — in Eastern Europe, Central and South America, the Middle East and all over Asia — are aware of NICE and are thinking about setting up something similar,” said Dr. Andreas Seiter, a senior health specialist at the World Bank.
Even in the United States, rising costs have led some in Congress to propose an institute that would compare the effectiveness of new medical technologies, although the proposals so far would not allow for price considerations. At the present rate of growth, medical costs will increase to 25 percent of the nation’s gross domestic product in 2025 from 16 percent, with half of the increase coming from new drugs and devices, according to the Congressional Budget Office.
To arrest this trend, the United States needs to adopt at least some of NICE’s methods, said Dr. Mark McClellan and Dr. Sean Tunis, who served earlier in the Bush administration as, respectively, administrator and chief medical officer of the Center for Medicare and Medicaid Services. Dr. Tunis said he spent a lot of time in government “learning about NICE and trying to adopt the processes and mechanisms they used, and we just couldn’t.”
That’s because the idea of using price to determine which drugs or devices Medicare or Medicaid provides has provoked fierce protests. But Dr. McClellan said the American government would soon have no choice.
Drug and device makers, which once routinely denounced the British for questioning product prices, have begun quietly slashing prices in Britain to gain NICE’s coveted approval, especially because other nations are following the institute’s lead. Companies have said that they will consult with NICE to help determine which experimental compounds enter the final stage of clinical trials, so the British agency’s officials will soon influence which drugs enter the market in the United States.
The British government created NICE a decade ago to ensure that every pound spent buys as many years of good-quality life as possible, but the agency is increasingly rejecting expensive treatments. The denials have led to debate over what is to blame: company prices or the health institute’s math.
Dr. Michael Rawlins, chairman of NICE, blames the industry, saying that some companies raise prices “to get profits up so their executives can get better bonuses.” Dr. Karol Sikora, a prominent London oncologist, said that the institute’s math was flawed and that Dr. Rawlins had a “personal vendetta” against cancer treatments.
Drug company executives who were interviewed uniformly promised to cooperate with NICE, but industry advocates were not so kind. Robert Goldberg, vice president of the Center for Medicine in the Public Interest, an advocacy group financed by drug makers, likened Dr. Rawlins and his institute to terrorists and said their decisions were morally indefensible.
Developing a Method
It all started with Viagra.
Pfizer’s introduction of the drug in 1998 panicked British health officials, who feared it would wreck the government’s health budget. So they placed restrictions on its use. Pfizer sued, claiming the government’s decision was arbitrary. To defend itself against similar claims, the government needed a standard method of rationing. The following year, NICE opened.
Asked whether he thought the institute would succeed, Frank Dobson, the Labor health minister at the time, famously said, “Probably not, but it’s worth a bloody good try.”
Britain’s National Health Service provides 95 percent of the nation’s care from an annual budget, so paying for costly treatments means less money for, say, sick children. Before NICE, hospitals and clinics often came to different decisions about which drugs to buy, creating geographic disparities in care that led to outrage. (Such disparities are common in the United States, even for federal Medicare patients.)
Now, any drug or device approved by the institute must be offered to patients. The institute has also written hundreds of treatment guidelines in hopes of improving, and making more consistent, basic medical care.
The institute has analyzed the cost-effectiveness of surgical operations, cancer screening tests and medical devices. For example, it found that drug-coated cardiac stents were worth only $450 more than bare-metal ones. In the United States, stent price differences are often far wider.
Five years ago, the British health institute recommended more emergency room CT scans of patients suffering from head trauma — forcing hospitals to buy more machines.
But the decisions that get the most attention are those involving new drugs. Any drug that provides an extra six months of good-quality life for £10,000 — about $15,150 — or less is automatically approved, while those that give six months for $22,750 or less might get approved. More expensive medicines have been approved only rarely. The spending limits represent the health institute’s best guess for how much the nation can afford.
After consulting a citizens group, the institute decided that the nation should spend the same amount saving or improving the life of a 75-year-old smoker as it would a 5-year-old.
‘Muddling Through’
The institute’s decision-making process involves a series of independent assessments, consultations with manufacturers, committee meetings, comment periods for outsiders and appeals that, taken together, Dr. Rawlins described as “procedural justice,” or “muddling through elegantly.” While the institute provides advice, decisions are made by one of three committees made up of doctors, nurses and economists from outside the government.
Transparency recently became a high priority, but gaps in the idea of openness remain. At the institute’s first public decision-making appraisal meeting in September, staff members handed a reporter a stack of documents, only to snatch them back moments later. The committee’s chairman, Dr. David Barnett, was so intent on keeping the meeting brief that he told a committee member: “This must be the last question. It must be relevant. Otherwise, you will feel my wrath.”
To analyze the value of the drug that Mr. Hardy, the kidney cancer patient, wanted, and the value of three other kidney cancer medicines, the British institute hired a university group that considered how many months the drugs delayed cancer’s progress.
Firestorm of Protest
The academics got drug prices and calculated the costs of administering them and treating their side effects. Not one of the drugs came close to being worth their expense, the group suggested. In a preliminary ruling in August, a committee from NICE agreed.
The decision caused a firestorm. Twenty-six prominent British oncologists wrote a letter to The Sunday Times saying that the institute assessed cancer treatments poorly and that patients were remortgaging their homes to buy drugs freely available in other countries.
Given that fewer than 6,000 people per year in England and Wales are diagnosed with kidney cancer, “Why put ourselves through so much heartache for very little money?” Andrew Dillon, the institute’s chief executive, asked in a September interview. “The answer is that if we don’t apply the same criteria even to small groups of patients, there’s little value to what we do at all.”
Dr. Sikora, who helped organize the August protest, predicted in a September interview that the institute would buckle under political pressure.
Flooded with anguished comments, the institute beat a hasty retreat. A preliminary consultation posted Nov. 5 said that the institute would instruct its appraisal committees to consider approving highly expensive life-saving drugs for terminal illnesses affecting fewer than 7,000 patients per year — a policy that seems tailor-made for Sutent and the three other kidney cancer drugs.
Negotiations with companies on possible discounts are continuing, and a committee is scheduled on Jan. 14 to make public this nascent compromise.
NICE has stood fast in other areas, though, rejecting Kineret for rheumatoid arthritis and Avonex for multiple sclerosis. In 2001, NICE ruled that Aricept and two other drugs used to treat Alzheimer’s disease were worth their costs only if patients’ conditions had increased from mild to moderate severity.
The analysis put a value on patients’ improved thinking skills, and possible savings from delayed entry into nursing homes. Instead of pills, the institute suggested more counseling.
Advocates for patients with Alzheimer’s disease called the decision heartless.
Dr. Rawlins said he was frustrated that his institute had been censured instead of the drug company executives who set sky-high prices. Take the case of Celgene, the maker of Revlimid, a drug for multiple myeloma, a bone-marrow cancer, that in a preliminary ruling on Oct. 28 the institute said was too costly.
Celgene’s first big seller was thalidomide, a decades-old medicine now used as a cancer treatment, which is so cheap to manufacture that a company in Brazil sells it for pennies a pill.
Celgene initially spent very little on research and priced each pill in 1998 at $6. As the drug’s popularity against cancer grew, the company raised the price 30-fold to about $180 per pill, or $66,000 per year. The price increases reflected the medicine’s value, company executives said.
In 2005, the company introduced Revlimid, a derivative of thalidomide that is supposed to be less toxic, but may be no more effective. Celgene priced it at about $260 per pill, or $94,000 per year.
Offering Discounts
Private and public insurers in the United States must pay whatever Celgene and other makers of unique cancer medicines decide to charge, so prices are soaring. Spending on cancer drugs and other such specialty medicines rose 9 percent last year and now represents 24 percent of the nation’s drug bill, according to Health Strategies Group, a New Jersey consulting company. Drug expenses in 2006 grew faster than any other part of the nation’s health bill except home care.
But because of the institute, Britain’s National Health Service has been among the first to balk at paying such prices, which has led many companies to offer the British discounts unavailable almost anywhere else.
Johnson & Johnson, for instance, agreed to charge for Velcade, another drug for multiple myeloma, only if tests showed it was effective in a particular patient. Novartis agreed to give free injections of Lucentis, a drug for age-related macular degeneration, if patients needed more than 14 shots. Dr. Rawlins said these deals were constructed by drug makers to hide from other countries the discounts offered in Britain.
“It’s a good deal for us, but I can’t see that it will work in the long run because I can’t see that others countries will be so dim as to not notice it,” Dr. Rawlins said.
A more prudent bureaucrat would never make such a remark. Dr. Rawlins said that he delighted in controversy, “although I’ll admit that it doesn’t always work out.” He wears thick glasses and fine suits whose pockets are stuffed with nicotine gum packages that rattle as he walks. He laughs easily, plays the piano and viola, and moves effortlessly between politics and medicine.
His criticisms of the pharmaceutical industry have sharpened.
“I want them to produce new drugs for conditions we really need treatments for, but I loathe their marketing practices, which corrupt doctors in a dreadful way,” said Dr. Rawlins, who until recently practiced general medicine and for years was chairman of the British version of the Food and Drug Administration. “And I’m very conscious that the prices the pharmaceutical industry charges are what they think the market will bear.”
In 10 years, the health institute’s budget has grown to $50 million from $13 million, and it is scheduled to rise to $142 million in four years. NICE has 270 employees, who include doctors, economists and pharmacists.
Worldwide Impact
Agencies like NICE are popping up across the globe. Dr. Leonardo Cubillos, Colombia’s national director of insurance, said that Colombia was using British methods to choose drugs for a national health insurance package.
Membership in an international group of drug and device assessment agencies grew to 45 last year from 8 in 1992. The British institute has created a consulting group to advise foreign governments.
Much of the reason for this proliferation of agencies is that, while prescription drugs represent just 10.3 percent of overall medical spending in the United States, that share is 17 percent on average in industrialized countries.
As spending on drugs soared in many nations — often haphazardly — overall health often showed little improvement. So international aid agencies are advising governments to adopt British assessments and deliberations to improve their public’s health while lowering costs, and officials are listening — a trend that is likely to accelerate during the present global economic slowdown.
The health institutes in both Britain and Germany may soon suggest prices for drugs, a strategy intended to deflect political pressure back on the companies and shorten negotiations that now often take months.
“We have been told that the price is the price, but the worm is turning now,” Dr. Barnett said.
Company executives acknowledge that they are increasingly acceding to British demands to slash prices.
But the most pressing question for the industry is what influence the British institute will have in the United States. The United States already spends more than twice as much per capita on health care as the average of other industrialized nations, while getting generally poorer health outcomes.
Michael O. Leavitt, the Bush administration’s secretary of health and human services, said in a September speech that, at its present growth rate, health care spending “could potentially drag our nation into a financial crisis that makes our major subprime mortgage crisis look like a warm summer rain.”
And while there is fierce disagreement about how and whether to control drug and device expenses as part of a broader reform of the health system, many say some cost controls are inevitable. At a September device industry conference in Washington, a seminar on the issue was standing-room only and half of the questioners mentioned NICE.
John R. Dwyer Jr., a Washington lawyer who represents device makers, said that many in the industry have believed that major changes to control costs in the federal Medicare program were inevitable, and “people see NICE as the only workable paradigm.”
Meanwhile, Mr. Hardy waits. In recent weeks his growing tumor has pressed on a nerve that governs his voice. He can barely speak and is increasingly out of breath. The Hardys are hoping that in January NICE will approve the use of Sutent, allowing Mr. Hardy further treatment.

11.28.2008

EU probe finds companies block cheap drugs

By Nikki Tait in Brussels

Published: November 28 2008

Drug companies have blocked or delayed the market entry of cheaper generic medicines to Europe, adding billions to the cost of medicines to patients, a high-profile report from Brussels has found. Anti-competitive practices range from initiating dispute and litigation to hold up competing products, and filing multiple patent applications for the same medicine, to concluding legal settlements with generic companies which constrain their ability to enter the market.
The European Comission report cited one example where “patent clustering” led to 1,300 patents being filed for a single medicine. Patent ligitation cases involving generics, meanwhile, lasted on average nearly three years, with the generic companies ultimately winning more than 60 per cent of these, it calculated.
Originator companies also concluded more than 200 settlement agreements with generic companies in the EU, according to the report. More than 10 per cent were “reverse payment settlements” which limited the entry of generic medicines and involved payments from the originator to the generics. These payments, the report says, totalled more than €200m.
“These preliminary results show that market entry of generic companies and the development of new and more affordable medicines is sometimes blocked or delayed at significant cost to healthcare systems, consumers and taxpayers,” said Neelie Kroes, EU competition commissioner, as she released the preliminary findings of a pharmaceutical sector inquiry.
Although the report does not name individual companies, Ms Kroes said there was likely to be follow-up action against companies which had breached EU laws.
“It is still early days, but the commission will not hesitate to open antitrust cases against companies where there are indications that the antitrust rules may have been breached,” she said.
But the pharmaceuticals companies accused Brussels of using ”selective quotations to mischaracterise the industry as anticompetitive”, and of overstating the level and reasons for delays in generic market access.
”The commission’s report does not substantiate in any respect their statement made at the opening of the inquiry that the industry is impeding innovation,” said Brian Ager, director-general of the European Federation of Pharmaceutical Industries and Associations.
The report comes days after the commission announced that it had launched dawn raids on a number of companies – including the UK offices of Teva, the world’s largest generic manufacturer - saying it was concerned about breaches of competition rules or abuse of a dominant position.
The report also backs changes to Europe’s patent system – including introduction of a community patent (a single unitary intellectual property right applying across the continent) and changes to its fragmented patent litigation system.
The sector inquiry was established this year, amid signs that there were fewer new medicines in the industry’s pipeline – a development which drug companies themselves say reflects changing a regulatory environment, rather than any abuse. It began in unprecedented fashion with dawn raids on the offices of large pharmaceutical groups, as the commission tried to gather evidence.

Copyright The Financial Times Limited 2008

11.20.2008

Deal reached on NHS drug prices

from BBC news

Drug costs will fall under the plan

The government and the drugs industry have struck a deal which could save the NHS in the UK up to £550m per year. A flexible pricing scheme will mean new drugs can be initially introduced at a lower price, which could be increased if the medicine proves effective.
There are set to be more schemes where the NHS and drug companies share the cost of innovative treatments. An Office of Fair Trading report last year said the NHS spent up to £500m annually on overpriced medicines. The deal is expected to save the NHS around £350m in 2009/10, and around £550m every year after that.In 2006/07, £10.6 billion - 12.7% of the total NHS budget - was spent on drugs.

A more flexible approach to pricing is in everyone's interest.

Health Secretary Alan Johnson

Under the current system, a drug company sets a price for a new medicine when it is launched, and there is little opportunity to change that - so firms set the price at what they think a drug will ultimately be worth, even if there is little evidence for that at the outset. The flexible pricing scheme aims to change that, and means a medicine's cost could go up - or down.

The cost of branded drugs will also be cut.

'In everyone's interest'

Overall, the cost of drugs is predicted to fall from 3.9% from February 2009 with a further cut of 1.9% from January 2010.

The government and ABPI will also look at introducing generic substitution from 2010 - which would mean a pharmacist could give out the cheaper non-branded version of a drug even if the GP had named the branded version on the prescription.

At the moment, that is not allowed.

Health Secretary Alan Johnson said of the new arrangements: "A more flexible approach to pricing is in everyone's interest.

"It gets clinically and cost effective drugs to more patients - providing cheaper options where clinically appropriate - delivers value for money for the NHS and the tax payer, and creates a better market for the pharmaceutical industry while supporting research and innovation."

Dr Richard Barker, director general of the ABPI said it was the first time the pricing agreement between the NHS and the drugs industry had not been purely a financial deal.

"This landmark deal marks a turning point for patients, the NHS and the pharmaceutical industry.

"It is an all-encompassing package that encourages the discovery of new, more effective medicines, while at the same time allowing NHS patients to access these treatments more quickly."

Risk-sharing

Nigel Edwards, director of policy at the NHS Confederation which represents NHS managers, said throughout the debate over top-up payments for cancer drugs, they had said one part of the solution had to be a new pricing model.

"It is good news that this is now starting to happen although we would caution that there needs to be care taken that this does not land doctors and nurses with a heavier workload of form filling and bureaucracy."

But shadow health minister Mark Simmonds said the government had damaged the UK's reputation as a base for the pharmaceutical industry and failed to address the issue of drugs being available to patients in Europe that are not available here.

And Liberal Democrat health spokesman, Norman Lamb said: "This new development is welcome but not enough on its own to deliver real change."

11.16.2008

Racing down the pyramid

Nov 13th 2008 | NEW YORK
From The Economist print edition

Big drugmakers’ love affair with America is coming to an end

FOR many years America has been the heart and soul of the pharmaceuticals business. The adoption of price controls and government-run health systems in Europe, where the industry began, led many drugs firms to pitch their tents in the land of the free market. Keen to encourage innovation and suspicious of big government (until recently, anyway), America has allowed drugs companies to price their wares more or less as they please. As a result, over half of the leading firms’ profits come from America alone. So it might seem odd to suggest that the industry’s future now lies in the developing world. Indeed, for years drugs firms resisted the trend, fashionable in other industries, towards pouring billions into emerging markets. They justified their stance by pointing to weak patent protection and low incomes in those markets. But now the industry has changed its mind. When he took over as boss of Britain’s GlaxoSmithKline (GSK) earlier this year, Andrew Witty declared that emerging markets would be at the heart of his growth strategy. GSK has since agreed a path-breaking licensing agreement with Aspen, a South African “branded generics” firm, and has just paid some $200m for Bristol Myers-Squibb’s Egyptian operations. For its part Pfizer, the world’s biggest pharmaceuticals firm, recently announced a restructuring that makes emerging markets a priority. Jean-Michel Halfon, who is in charge of that effort, says serving customers in developing countries is now “a business, not a charity.” Why the U-turn? The tremendous growth of drugs markets in the developing world proved too tempting to ignore. IMS, an industry consultancy, forecasts that sales in the biggest emerging markets will hit $300 billion by 2017, equal to today’s sales in the top five European markets and America combined. Even before the latest downward lurch in prospects for rich economies, growth in those countries was expected to be much slower than in big emerging markets (see chart). If growth is the carrot luring the drugs giants into emerging markets, the stick is the change in regulatory outlook in America from friendly to possibly frosty. The industry is concerned that Barack Obama, once in office, might allow cheap drugs to be imported from Canada or force Medicare, the government health-care system for the old and disabled, to negotiate big discounts with drugs firms. Peter Lawyer of Boston Consulting Group estimates that the latter reform alone could reduce the industry’s American revenues by 3-10%. In fairness, any move by Mr Obama towards universal health-coverage could boost drugs sales by giving more people insurance, but the industry nevertheless worries about a squeeze on margins. Hence the industry’s zealous push into places like China and India. But if it is to succeed in emerging markets, its strategy and tactics will have to change. In the past, observes Loic Plantevin of Monitor, a management consultancy, Western drugs firms did not fare well because they often lazily “recycled” the products and marketing plans that worked in America for use in poorer countries. But now he thinks firms are doing better. Some are offering products of particular relevance to developing countries, such as treatments for hepatitis B, or combination therapies, which are especially popular in India. Western firms have also dropped their traditional resistance to tiered pricing: Pfizer’s Viagra, a drug for erectile dysfunction, and Merck’s Gardasil, a vaccine against cervical cancer, were both introduced in India at a fraction of their American price. The health-care arm of Bayer, a German conglomerate, has seen its sales in emerging markets soar as it has included more locals in drugs trials and brought new pills to market soon after launching them in America. Some firms are going further, venturing beyond the familiar big cities to more difficult, but potentially more lucrative, territories. Mr Halfon says Pfizer has expanded in the past couple of years into over 130 Chinese cities. His firm has also set up a joint venture with Grameen Bank in Bangladesh to cultivate rural markets for basic drugs by developing “microinsurance” products. Mr Halfon is convinced there is plenty of money to be made among the underserved poor. He thinks the drugs market for those earning less than $3,000 a year is already worth $30 billion annually, and he expects this to increase to $60 billion-70 billion by 2012. Novartis, a Swiss rival, recently unveiled a pilot project to expand into rural India; the firm aims to reach 50m new customers by 2010. Further evidence of emerging markets’ potential comes from the experience of Britain’s AstraZeneca in China. Unlike rivals, which focused on Shanghai and Beijing, its trailblazing marketers pushed into the country’s remote western provinces. The going was tough, but with little foreign competition the firm’s efforts paid off. It has just reported that during the third quarter, sales in mature markets grew by 2% compared with the same period a year ago, but increased by 35% in China—and by 18% in emerging markets overall. It seems that there is indeed a fortune at the bottom of the pyramid.

11.14.2008

ISPOR Athens 2008 re-cap

Hello everyone,

back from 14 days of travel I thought I put together a short note on this year's European ISPOR conference in Athens. Certainly the venue was so much better than last year, and the weather for early November couldn't have been nicer, especially over the weekend. Needless to say that Athens had a lot to offer from cultural aspects to entertainment. Hope you all checked out the view from the Galaxy bar at the Hilton - the illuminated Acropolis by night, just amazing.
I have been networking and doing lots of internal stuff therefore didn't attend too many sessions. Just a few comments therefore on points I personally found interesting.
The harmonization discussion of the first plenary session was obviously not new and the idea still reminds me of the approaches taken by centralized economies of the former Eastern socialist block where many people seemed to believe that centralization and broad government interference and small long term planning committees will know better about the preferences of individuals and society, instead of letting the mechanisms of 'trial and error' combined with some healthy competition find out what might work best in each setting. From that perspective, the outcome of this session was to be expected - harmonization of methods and frameworks perhaps possible and useful to some extend, decision making and cost-effectiveness is a local matter - well, what else and rightly so. This topic is now probably sufficiently discussed and needs no repetition.
The old QALY discussion has not come too any new insights either, however here I find is still some work to be done as I am a strong believer that the QALY doctrine of some countries needs to be revisited - especially for the patient's benefit.
The second plenary about improving equity of access was an interesting debate from my perspective, I especially liked the presentation of Tienne Stander from South Africa. A while ago we both presented on biologic treatments at a South African health conference and the wide open discrepancy of basic health care needs versus the availability of highly sophisticated treatment options are especially pronounced in his country and is in need of actions. However, as long as the current health minister down there believes that HIV can be cured with herbal remedies, there is still a long way ahead.
On the poster front I noticed an increasing amount of work in the vaccine area, which I found very interesting as epidemiological models have gotten so much better. Also Oncology - needless to say - was broadly represented.
I haven't paid too much attention to the booths etc. but the usual "suspects" ;) and some new consulting companies where widely represented. Here it remains to be seen how the market will shape the scene up. Clearly with current restructuring in industry and the build up of broader market access capabilities, consultancies who get better at broader economics, understanding of payer systems and pricing strategies / deals will be better positioned as I believe we do not need to invest so much more in statistical model overkill, at least in most areas.
By the way, everyone I was talking to was anticipating the second Latin American conference In Rio de Janeiro, Sep. 2009 to be a huge success - I already offered my Brazilian colleagues a lot of support in order to make that event happen myself ;)

I guess I'll see you all over Caipirinha next year!

As always, best wishes
Ulf