Almost one year ago, the Secretary-General of the United Nations
convened a High-Level Panel on Access to Medicines, which is especially limited
among the poor in parts of the developing world still suffering the burden of
tropical diseases (such as river blindness, sleeping sickness, leprosy, and
rabies.) According to World Health Organization, 1.7 billion people in 185
countries needed treatment for neglected tropical diseases in 2014.
In the 21st Century, such numbers are shocking. However, the
panel’s recommendations would have many harmful effects on the development of
new medicines that benefit patients in both the developing and developed world.
Indeed, it identifies the wrong culprit in the ongoing health catastrophe in
the developing world.
Rather than allow the current decentralized system of primarily
private for-profit - supplemented by some government and philanthropic -
funding for researching, developing, and distributing new medicines, the panel
recommends governments take over this function. And not even governments acting
independently, but a sort of supra-national cartel would dictate how the
world’s R&D budget would be spent.
Specifically, the panel advocates that governments “negotiate global agreements
on the coordination, funding, and development of health technologies.” The
funding would come from “transaction taxes and other innovative financing
mechanisms.” (Only a panel mostly comprised of public-sector veterans would
describe tax hikes as “innovative financing.”)
The report estimates $240 billion was invested in medical
R&D in 2009 and 2010, of which $144 billion was from the private
sector, $72 billion from the public sector, and $24 billion from the non-profit
sector. Ninety percent was from highly developed countries, especially the
U.S., which the panel recognizes holds a “central position in health technology
innovation.”
The purpose of a multi-lateral government cartel seizing control
of this capital would be to cause a “delinkage” between R&D spending, prices
and consumer costs. In other words, investors would no longer be allowed to
execute business plans that channeled R&D funding to profitable
therapies.