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N Engl J Med. Poverty, Wealth, and Access to Pandemic Influenza Vaccines

Giuseppe

Emeritus
Poverty, Wealth, and Access to Pandemic Influenza Vaccines (NEJM, full text, edited)
Published at www.nejm.org August 12, 2009 (10.1056/NEJMp0906972)

Poverty, Wealth, and Access to Pandemic Influenza Vaccines


Tadataka Yamada, M.D.


On June 11, 2009, Margaret Chan, director general of the World Health Organization (WHO), declared that the status of the influenza A (H1N1) pandemic had reached phase 6 ? active transmission on a global scale. Until now, the case fatality rate of this influenza has been quite low, but history teaches us that the situation could take a turn for the worse during the next wave of the pandemic.

If a 1918-like pandemic were to occur today, tens of millions of people could die, the vast majority of them in the world's poorest countries.

Fortunately, the prospects for developing an effective vaccine to prevent infection with the current H1N1 virus are excellent, and the world's pharmaceutical companies are working diligently at this task. In contemplating equal access to such a vaccine, it is important to consider three key issues: manufacturing capacity, cost, and delivery.

Only a few countries in the world have plants for manufacturing influenza vaccine, and three companies ? GlaxoSmithKline, Sanofi-Aventis, and Novartis ? account for most of the world's manufacturing capacity. The number of doses of vaccine against H1N1 influenza that could be produced with the existing capacity is very large, but the sobering truth is that even if production were switched over completely from seasonal influenza vaccine to pandemic influenza vaccine, there would not be nearly enough for everyone in the world. The size of the gap in potential supply depends greatly on the dose that is required, and it may be possible to reduce the necessary dose by as much as 75% with the use of an adjuvant. The challenging problem is that much, if not most, of the manufacturing capacity is already spoken for through purchasing contracts held by many of the world's wealthy countries.

The second issue is cost. Despite the enormous technological investment required to create a vaccine, the traditional cost of seasonal influenza vaccines even in wealthy countries is quite low. For the pandemic H1N1 influenza vaccine, the major manufacturers have indicated a willingness to offer tiered pricing, with affordable prices for poor countries. Going even further, Sanofi-Aventis has committed to donating 100 million doses of its vaccine to a stockpile for poor countries, and GlaxoSmithKline has committed to donating 50 million doses. Nevertheless, financial commitments from wealthy countries will be needed to help poorer countries purchase vaccines ? cost should not be a barrier to access.

Finally, the scope of access to vaccines will in part be determined by the infrastructure required to deliver them to all citizens in mass campaigns. Ironically, poor countries may have an advantage on this front, since many have recent experience with mass campaigns involving vaccines against polio, measles, and hepatitis B; delivery may therefore be less of a challenge for them, provided that the vaccines reach them in a timely fashion. By contrast, in many wealthier countries, such campaigns have not been undertaken for some time. Getting the vaccine to large numbers of young adults, in particular, may be a formidable task for which preparations must surely be made as soon as possible.

Our limited capacity for producing potentially lifesaving vaccines presents a pressing moral challenge. I believe wholeheartedly that all lives have equal value (this is the basic principle motivating the Bill and Melinda Gates Foundation, where I work), and I believe that every stakeholder has a responsibility to ensure that the pandemic does not take a 1918-like toll on the world. We have therefore worked with partner stakeholders to develop a proposed set of principles to guide the global allocation of pandemic vaccine (see Principles to Guide Global Allocation of Pandemic Vaccine).

Rich countries have a responsibility to stand in line and receive their vaccine allotments alongside poor countries, even if they have paid for their vaccine before others could do so. It would be inexcusable to force poor countries to wait until the rich have been served under their existing contracts with vaccine manufacturers. Moreover, rich countries must also consider how they can provide contributions to offset the cost of vaccines for countries that cannot afford to pay for them. Countries that are home to influenza-vaccine manufacturing plants have a special responsibility to avoid nationalizing those facilities in an effort to reserve their output for their own citizens before others. And all countries must prepare now for the rapid delivery of the vaccines as soon as they become available.

Manufacturers have a responsibility to apply their full capabilities to creating the greatest possible quantity of vaccine doses. Despite contractual obligations to supply many wealthy countries with their vaccines, manufacturers must resist the temptation to commit all their capacity to those who can pay the most. This is not a time to adhere to the "first come, first served" model of business, since we may be facing a health crisis of global proportions in which all people and countries are equally at risk. To ensure fairness, full adherence to a tiered pricing scheme in which the cost to the purchaser is proportionate to its ability to pay is essential. The generous donations made by Sanofi-Aventis and GlaxoSmithKline set an example that all manufacturers should emulate. In return for their responsible actions, it would be reasonable for manufacturers to be indemnified against liability from potential adverse reactions to their vaccines.

Regulatory agencies have an important responsibility in this impending crisis because they stand between the manufacturers of pandemic influenza vaccines and the people who will benefit from them. It is critically important that regulators apply their usual rigorous standards in approving the new vaccines ? but also that they do so in a timely fashion. A special task facing them is the rapid review and consideration of the safety and efficacy of adjuvants, whose use could greatly reduce the required dose of vaccine and thereby expand the number of doses that could be manufactured.

The WHO has provided strong leadership as the world has contemplated the prospect of an influenza pandemic. We are counting on the organization to guide us, wisely and fairly, through the complex challenges that lie ahead.

The prospect of a worsening global influenza pandemic is real and will not go away anytime soon. I cannot imagine standing by and watching if, at the time of crisis, the rich live and the poor die. It will take collective commitment and action by all of us to prevent this from happening.


Principles to Guide Global Allocation of Pandemic Vaccine.


1. The global community should take steps to protect all populations, including those without resources to protect themselves.
2. Vaccination should be considered in the context of comprehensive pandemic preparedness and response efforts in all nations.
3. Developed countries and vaccine manufacturers should urgently agree upon a mechanism to ensure access to vaccine by developing countries.
4. Influenza vaccine manufacturers should identify strategies such as tiered pricing and donations to make pandemic vaccine more accessible to developing nations.
5. Pandemic vaccines allocated to developing nations should become available in the same time frame as vaccines for developed nations.
6. The global community should obtain data to help establish a consensus on the safety and efficacy of adjuvants, and efforts should be made to ensure the fullest use of this and other dose-sparing strategies.
7. All countries obtaining pandemic vaccine should ensure that mechanisms are in place to provide the vaccine to their populations, to ensure that this scarce resource is not wasted, and donors should be prepared to provide resources and technical assistance to help countries bolster these mechanisms.
8. The World Health Organization is uniquely positioned to lead the global response to a pandemic virus and should support governments and industry in their efforts to implement these principles.

* From the Pneumonia and Flu Web site of the Bill and Melinda Gates Foundation (www.gatesfoundation.org/topics/Pages/pneumonia-flu.aspx).

Dr. Yamada reports holding equity in GlaxoSmithKline. No other potential conflict of interest relevant to this article was reported.

Source Information
From the Global Health Program, Bill and Melinda Gates Foundation, Seattle.
This article (10.1056/NEJMp0906972) was published on August 12, 2009, at NEJM.org.
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<cite cite="http://content.nejm.org/cgi/content/full/NEJMp0906972?query=TOC">NEJM -- Poverty, Wealth, and Access to Pandemic Influenza Vaccines</cite>
 

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Re: N Engl J Med. Poverty, Wealth, and Access to Pandemic Influenza Vaccines

Another challenging fact is that some of the affluent nations where multi-national pharmaceutical corporations have influenza vaccines manufacturing facilities, have not the control on the industries, and thus everything is produced is totally under control of the owners, private and profit-driven.

Certain of the EU coutries decided to not decide about manufacturing of live-saving pharmaceuticals and drugs, thus some governments purchased the vaccines instead to drive the corporations with opportune policies...

So, the vaccine - for a number of affluent countries population - will arrive too late and in too little amount...

For the rest of the world, readers are free to imagine the real prospects.
 
Re: N Engl J Med. Poverty, Wealth, and Access to Pandemic Influenza Vaccines


H1N1 vaccine wars to plague world



Sat, 15 Aug 2009 17:58:03 GMT



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By Patricia Khashayar, MD., Press TV, Tehran

While nearly every country in the world has been swarming with the swine flu virus, scientists have not yet succeeded in producing a vaccine for the deadly virus responsible for more than 1,462 deaths.

The rapidly growing number of swine flu cases has given rise to the theory that everyone is immunologically vulnerable to the disease, indicating that the need for a vaccine is pressing particularly now that the flu season is nearing.

WHO officials have predicted that the estimated number of cases infected with the new flu virus, responsible for the first pandemic in the past 41 years, will reach two billion in the next two years, making it even more dangerous than earlier pandemics which have infected one-third of the world's population.

Unless an effective swine flu vaccine is developed and successfully produced, experts predict that several hundreds of thousands of individuals could die worldwide.

Governments and scientists are in the race to produce an H1N1 vaccine. Sanofi-Aventis -- the world leader in flu immunization, Novartis AG, Baxter International, Schering-Plough's Nobilon, GlaxoSmithKline Plc, Solvay, Australia's CSL Ltd, and AstraZeneca's MedImmune are among the companies working on this vaccine.

Regulators in Europe and the US plan to fast-track the approval of swine flu vaccines to ensure their mass production before the start of winter in the northern hemisphere.

They, however, have asserted that the safety of the drug should not be compromised by hast to produce a vaccine.

In order to achieve such goal, four 'mock-up' vaccines developed by Baxter, GlaxoSmithKline and Novartis have already been approved in the European Union based on earlier data generated with the H5N1 virus strain, which is similar to H1N1.

The main cause of such fast approvals was that previous studies on seasonal influenza vaccines had shown that inserting a new strain in a vaccine - as in mock-up vaccines for changing H5N1 to H1N1 - does not substantially affect the safety or level of protection offered by the vaccine.

Aiming to produce effective vaccines for the fastest-moving pandemic ever seen, different pharmaceutical companies have adopted different manners.

Many are using conventional egg-based technology and particles of the dead virus, as they believe that while the method is time-consuming it blocks any possible way for the transmission of influenza from the vaccine.

Novavax Inc, on the other hand, is using a gene sequence provided by the US Centers for Disease Control for producing a virus-like particle, which is not capable of replicating, with the aim of producing the vaccine in a shorter time.

Unlike currently available flu shots, AstraZeneca's MedImmune is using weakened strains of the virus for developing vaccines in the form of nasal spray.

It should be noted that the use of a dead virus or particles unable to replicate in these vaccines is aimed at preventing catastrophes such as what happened during the H1N1 outbreak in 1976, when hundreds of people developed Guillain-Barre Syndrome -- an inflammatory disorder of the peripheral nerves characterized by ascending paralysis -- a few weeks after receiving the vaccine.

Aiming to overcome the fear regarding the side effects of the vaccine, Australia (Adelaide-based Vaxine Pty Ltd and Melbourne-based CSL Biotherapies in partnership with CMAX, a clinical research organization, and Royal Adelaide Hospital) and China have launched large human trials.

Despite suppositions that companies would face difficulty finding volunteers for testing the vaccine due to the 1967 vaccine incident, many who feared contracting the 'unstoppable' virus queued up to receive the newly produced vaccines.

Several other manufacturers including Swiss-based Novartis, Paris-based Sanofi Pasteur and a number of other firms in the US have also started or will soon begin such trials.

Experts hope to conduct similar trials in children as soon as the released information confirms the safety of the product in adults. They also hope to estimate the global supply of the vaccine, the number of doses required for each individual as well as the quantity of active ingredients (antigen) needed in each vaccine dose based on the results of these trials.

Despite all these efforts, questions remain about when a swine flu vaccine will become available. WHO officials, hence, believe a fully licensed vaccine might not be ready earlier than fall.

Moreover, many believe certain countries particularly developing ones will not be able to receive their required vaccine until January 2010 due to the lengthy order list and overwhelming demand for the vaccine.

At least 50 governments have placed orders or are currently negotiating with pharmaceutical companies to secure supplies of under-development H1N1 vaccines. England, Australia and Germany have already ordered large quantities, enough for their entire population.

US officials also hope to have 160 million doses of the injectable swine flu vaccine on hand by October, with more doses coming in the form of a nasal spray. Officials, however, believe even these high doses would be sufficient for only a fraction of the population at-risk of contracting the new influenza strain.

Despite all these contracts and orders, public health officials foresee "vaccine wars", an ugly scramble over the swine flu vaccine when it becomes available.

"Pandemic vaccine will be a valuable and scarce resource, like oil or food during a famine," said David Fidler, a professor of law at Indiana University who has consulted for WHO. "We've seen how countries behave in those situations, and it's not encouraging."

Experts warn that during a global epidemic, such as what the world is experiencing now, countries with flu vaccine plants might decide to seize all vaccines, aiming to first protect their own citizens before allowing companies to export the vaccine.

Such an act, hence, would break the pharmaceutical contracts promising other countries vaccine supplies, leaving countries such as Britain and the US - which import all or the majority of the flu vaccines they use -- not only without vaccine, but without legal recourse.

"There's nothing in international law that helps you resolve this, it's just a political nightmare happening in the midst of an epidemiological nightmare," added Fidler.

Meanwhile, in order to overcome the fear regarding the shortage of vaccine in poor nations, several pharmaceutical companies have promised to provide developing countries with certain amounts of the vaccine at a reduced price when they become available. Two manufacturers have guaranteed to give out 150 million doses for health workers in poor countries.

Considering the limited amount of vaccine, countries are identifying their at-risk population with the aim of curbing the spread of the disease with their restricted vaccine quantity. Experts, however, are not sure whether individuals would be willing to skip getting a vaccine, if there are to be limited swine flu shots.

WHO officials believe healthcare workers should be the first to be immunized in all countries in order to retain a functional health system as the virus evolves. Pregnant women and immunosuppressed individuals are also on top of the list.

UK officials, however, have included drug addicts on methadone in the group who will be given priority for the vaccine. Many, however, believe the revelation of such decision would lead to disagreements at a time when there is increasing public concern over swine flu.

Despite all these limitations, many governments are relying on these vaccines to contain the spread of the disease, providing a potential sales windfall for the companies that are able to deliver quickly and in large volumes. With little or no safety data about the swine flu vaccine, these governments are planning to conduct mass inoculation programs as soon as the vaccine becomes available, an act considered as a gamble by many individuals.

Many governments have decided to protect their citizens against the new flu with the seasonal flu vaccine for the time being, saying that both diseases stem from the same ?A? virus strain.

Reports, however, suggest that the vaccine can only reduce the chances of contracting the H1N1 virus by 50 to 60 percent.

http://www.presstv.ir/detail.aspx?id=103589&sectionid=3510304


 
Re: N Engl J Med. Poverty, Wealth, and Access to Pandemic Influenza Vaccines

This is the results of decades of public health investments and fundings cuts all around the world.

It is also unlikely that the people involved in these policies will perform apology for the detrimental effects in special mode toward the developing world nations, the most affected by the cuts.

Now, when the events are running and time to do anything useful is short, some opinionists are pointing toward the scarcity of vaccine and other live-savings drugs and equipment.

I would ask them: ''Hey, people, when certain economics schools leaders pushed for public health privatizations and for the creation of a profit-driven system even in the poorest nations, I haven't heard nothing from you!''

Now, the vaccine may be a mirage for the most part of the world population, with the help of a - to date lacking - strong political leadership for an improved international cooperation and assistance.

The fact - then - that a vaccine could protect only for the 50/60% from developing the illness, well, if this is enough to save more people from severe complications, it is a good news.

We are unlucky: the damages done in the last two or three decades cannot be repaired in two or three months.

Sooner this is acknowledged, sooner we will start to understand the events.
 
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