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Run-AMCThe latest idea in vaccine funding won't cure AIDS and malaria.

Is he getting the best vaccine? Click image to expand.The quest to save the world with vaccines has been faltering. After increasing during the 1970s and '80s, vaccination rates have fallen since about 1990 for basic diseases in developing countries. Development of vaccines for emerging and expanding diseases (like AIDS and malaria) has also moved haltingly. Only half the children in sub-Saharan Africa get basic vaccination for diphtheria, tetanus, pertussis, and measles; rates for those vaccines in some countries have dropped below 25 percent. Every year, 10 million people die from diseases for which vaccine development or delivery is lagging.

Drug companies spend little to produce or distribute vaccines for developing-world diseases because that's not where profits lie. Recently, however, health-policy experts have been floating a newish way to prod the industry into action: the advanced market commitment. The AMC is a promise by a donor country or organization to reward the development and production of a specific vaccine by buying upfront a certain number of doses at a price that will ensure the drug developer a healthy return. Since the typical earnings of a successful new drug are about $3 billion, AMC advocates suggest that sum as the promised return for each new vaccine. So, if the United States and Europe want to inspire production of 200 million treatments of malaria vaccine, they would promise $15 a treatment—for $15 x 200 million treatments, or $3 billion—to the first vaccine maker that develops, tests, and brings to market the specified vaccine. Though technically not a prize, the AMC creates a sort of race: The money is awarded not through a contract but to the first company that successfully completes all trials and has a vaccine ready for manufacture. The "pull" of this demand is meant to complement the "push" of grants for drug research and development.

Variations of the AMC have been around for nearly a decade, but its current form and name come from "Making Markets," a report produced last April by the Center for Global Development, a small but influential anti-poverty think tank, and written by Harvard economist Michael Kremer with the CGD's Owen Barder and Ruth Levine. The idea quickly caught on. In September, a bill designed to raise vaccination rates in developing countries, introduced by Sens. Richard Lugar, R-Ind., and John Kerry, D-Mass., included AMC funding as a key element. In December, Britain announced it would fund AMCs for malaria and AIDS vaccines, and other European Union countries said they would consider doing so in 2006.

But even as the AMCs' momentum built, some of the experts who advised the group that wrote "Making Markets," including Oxford economist Andrew Farlow and Princeton health-policy specialist Donald Light, charged that Kremer and his co-authors had ignored problems that make AMCs clumsy and inefficient—and likely to inspire mainly mediocre vaccines. The heart of the Farlow group's criticism is that AMCs by their nature will produce not the best drugs that money can buy but those that are quickest and least expensive to bring to market. To motivate drug companies, an AMC sets specifications for the desired vaccine that seem realistic at the time. Like all drugs, however, vaccines typically take a decade to develop. And in light of research developments in those intervening years, the original specs may prove quite unambitious. But the AMC would still go to the first drug company to produce and test a vaccine that meets the predetermined minimum specs.

Consider, for instance, an AMC for a malaria vaccine that effectively inoculates 60 percent of the people who get it. Four years into its research, Company A makes a breakthrough that makes it possible to achieve a 90 percent rate of inoculation. But Company B gets its 60 percent-effective vaccine to market first. Company B gets the prize; Company A gets nothing—and its vaccine never gets developed. Farlow notes that many AMCs could go not to new vaccines but to existing products that drug makers developed and then shelved because they lack profit potential.

The winner-take-all nature of AMCs and the long path of drug development, then, could allow mediocre drugs to capture most AMC rewards. A fresh round of AMC funding could be offered for a second, better vaccine. But companies that lost out the first time couldn't count on new money, so, until it appeared, development of potentially superior vaccines could stall. The basic flaw is that AMCs tend to attract easy solutions to disease and discourage more ambitious ones. As Farlow and his group point out, this hardly resembles a fluid, dynamic market in which buyers and sellers haggle over terms to determine value. And the problems seem either inherent to the AMC concept or remarkably intractable: Despite the expenditure of a lot of time and money, they've gone uncorrected since at least 1999, when AMCs were the subject of an intensive colloquium put on by the Sabin Vaccine Institute.

Kremer's response to this critique is incomplete and unsatisfying. He and his co-authors attribute the Farlow group's criticisms to ideological differences over whether market incentives have a place in public-health initiatives. In response to Farlow's practical beefs, Kremer says little. Addressing the charge, for instance, that many AMC rewards will go to less-ambitious, on-the-shelf vaccines, Kremer asserts that AMCs "can … be designed to create incentives for new products and competition." But he doesn't say how. Instead, he simply restates criticisms he has made of the existing system for vaccine production that AMCs are supposed to address.

Kremer's main target here is the primary engine of present efforts to increase vaccination rates in the developing world: public-private partnerships. Through PPPs, drug companies develop vaccines in conjunction with nonprofits like the Bill & Melinda Gates Foundation or government agencies like the National Institute of Allergy and Infectious Diseases. The AMC crowd assumes that PPPs won't suffice since they've presumably allowed the recent declines in investment and vaccination rates. But that premise is wrong. The declines are primarily the result of the consolidation of drug companies, which reduces innovation, and the increasing emphasis on creating and marketing blockbuster drugs, which discourages investment in less-profitable vaccines.

Despite these shifts in the market, PPPs have made a dent during the last five years or so in developing the vaccines that poor countries need. PPPs created the malaria vaccine that recently produced such encouraging trial results in Mozambique, for instance. Such partnerships have also advanced AIDS vaccine efforts, cut measles deaths significantly, and eradicated the deadly Hib virus in Gambia. At first glance, the AMC looks like the alphabet-soup option of choice. But its problems have proved terribly stubborn. At this point, like so many market offerings, it appears to be oversold.

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David Dobbs, the author of three books, writes on medicine, science, and culture for publications including Slate, the New York Times Magazine, Scientific American, and National Geographic. He blogs at http://scienceblogs.com/neuronculture.
Photo of Somalian child receiving vaccination by Simon Maina/AFP Photo.
COMMENTS

Remarks from the Fray:

Thank you to Slate and David Dobbs for drawing attention to the challenge of developing vaccines for diseases that kill millions of people each year in developing countries, such as malaria, tuberculosis and HIV ("The latest idea in vaccine funding won't cure AIDS and malaria".) Our proposal for sponsors to guarantee to pay for new vaccines if they are developed has been well received by governments, the biotech and pharmaceutical industry, leaders in public health, and numerous public-private partnerships working on the development of new medicines. A wide range of experts recognizes that Advance Market Commitments have the potential to stimulate development of, and access to, desperately needed new vaccines by creating market incentives for the firms similar to the incentives that they have to develop new medicines for rich countries.

Mr Dobbs suggests that the Advance Market Commitment proposal may be difficult to implement in practice. But the criticisms he cites are the result of a misunderstanding of what is proposed. We are happy to be able to clear them up now.

An Advance Market Commitment would not be "winner-takes-all". As Mr Dobbs rightly points out, that could lead to donors rewarding the manufacturer of an inferior vaccine that is produced quickly, instead of a preferable vaccine that could be developed later. In Making Markets for Vaccines (Chapter 3: Market Not A Prize) we explain how demand would be able to shift to the best available qualifying vaccines – in other words, the subsidy would go to better vaccines when they are available. This mechanism should allay any concern that there might be an incentive to develop mediocre vaccines quickly. The incentive is for manufacturers to invest private capital to create the best possible vaccine as quickly as they can, so that they capture the largest possible share of the premium market. It is designed to be a close parallel to the market for medicines in affluent countries – much more like the market that produces the medicines on which we and our children depend than a system that depends entirely on public or charitable funding.

Mr Dobbs implies that there is a tension between supporting Advance Market Commitments and supporting public-private partnerships for the development of new vaccines. He says, "the AMC crowd assumes that public private partnerships won't suffice since they've presumably allowed the recent declines in investment and vaccination rates." In fact, these partnerships are a key part of "the AMC crowd" – the idea is supported by all the main partnerships working on vaccines for neglected diseases, such as the Malaria Vaccine Initiative, the International AIDS Vaccine Initiative, the AERAS Global Tuberculosis Vaccine Foundation, and PreventPneumo, all of which have encouraged policymakers to pursue the Advance Market Commitment approach. These partnerships are at the forefront of the recognition that commercial investment by the private sector is an essential complement to public funding to accelerate new vaccines – which is precisely what the commitment is designed to achieve.

Mr Dobbs complains that our 13-page response to these criticisms is "incomplete and unsatisfying" and worries that the design problems may be "intractable". But as we have seen, the criticisms are of a proposal that nobody is making. Rather than defending a straw man, the broad group of experts that developed the Advance Market Commitment has been developing a detailed proposal for implementing the idea, working with the partnerships, industry representatives, the public health community and the G8 governments. As the Italian Finance Minister's report to the G7 Finance Ministers in December concluded, there is a widespread consensus among all the key stakeholders that Advance Market Commitments can be implemented in a way which, together with other sources of funding and working with the public private partnerships, could accelerate the development and use of new vaccines. That is why the G7 Governments have decided to pilot the idea during 2006.

We welcome this discussion of the Advance Market Commitment proposal set out in the Making Markets for Vaccines and its subsequent evolution, and we would be happy to answer any questions. This is an excellent time to The G7 Governments, industry and public health community, are now working together to finalize the details of the pilot Advance Market Commitment, to harness the resources, energy and expertise of the biotech and pharmaceutical industries to tackle the world's most pressing health problems.

Owen Barder
Michael Kremer
Ruth Levine

Co-authors, Making Markets for Vaccines

(To reply, click here)

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