[Ip-health] UACT March 8, 2018 Testimony at 2018 Special 301 Hearing
kim.treanor at keionline.org
Thu Mar 8 12:45:43 PST 2018
UACT March 8, 2018 Testimony at 2018 Special 301 Hearing
On Thursday March 8, 2018, the Union for Affordable Cancer Treatment
delivered the following testimony at the hearing for the 2018 Special 301
list. The testimony was delivered by Dr. Manon Ress.
To see previous UACT written submissions and testimonies to the Special 301
review process, please visit our page on our work concerning the Office of
the US Trade Representative.
Prepared statement of UACT (PDF), for March 8, 2018 hearing on the USTR
Special 301 list
Docket No. USTR-2017-0024
My name is Manon Ress. I am speaking today on behalf of the Union for
Affordable Cancer Treatment, which filed comments in this docket on
February 6, 2018.
The Union for Affordable Cancer Treatment (UACT), created in 2014, is
concerned about the rapidly escalating costs of cancer medication in the US
and globally, and we are committed to universal access to new technologies
at affordable prices.
Based on the process that brings us here as well as comments provided by
industry representatives, the staff of USTR will, “call out foreign
countries and expose the laws, policies, and practices that fail to provide
adequate and effective IP protection and enforcement.” USTR says one of
the, “top trade priorities for the Trump Administration is to use all
possible sources of leverage,” in order to ensure, “that U.S. owners of IP
have a full and fair opportunity to use and profit from their IP around the
What’s wrong with this?
The “Administration’s aggressive efforts to defend Americans from harmful
IP-related trade barriers” means, in plain language, in regards to new
drugs, vaccines and diagnostic technologies, higher prices. Higher prices
mean several things for patients, which is just another word for people,
people who are injured or have a disease or condition that requires a
treatment that involves a new drug.
Higher prices mean that many people, and indeed most people who need a new
drug, won’t have access. And those who do may face financial hardships, a
financial calamity coming on top of medical calamity.
That’s what PhRMA wants from you. They want you to use “all possible
sources of leverage” to make drug prices higher. They want you to create a
political landscape where countries like Colombia, Chile, Peru, Thailand,
Brazil, Malaysia, Indonesia, South Africa, India and even the Netherlands
do not use lawful compulsory licenses to address excessive pricing on new
drugs. You are supposed to be the defenders of the unfettered monopolies on
life saving technologies.
If you succeed, people will die, and people will suffer, and health care
budgets will waste scarce resources on over-priced medicines.
UACT is opposed to this approach. UACT does not want USTR to put patents
before patients, or drug companies before people.
UACT is also committed to robust innovation, and we know that this depends
upon access to knowledge and both public and private sector investments in
Because UACT favors both innovation and access, we support efforts in the
U.S Congress and around the world to reform our system of financing medical
We want governments, including the United States, to progressively delink
the incentives to invest in R&D from the prices of products.
We also want the global negotiations on innovation to stop focusing solely
on private sector incentives, like patent monopolies.
In creating global norms on R&D funding, governments need to embrace more
inclusive approaches, that recognize the value and importance of public
sector investments in biomedical R&D. The United States is a world leader
in public sector funding of R&D, through such agencies as the NIH, BARDA,
the National Sciences Foundation, the Departments of Defense, Veterans
Affairs, and Energy. USTR should be encouraging other governments to step
up their public sector funding of biomedical R&D, including most
importantly the elements that become public goods, advancing medical
UACT is concerned about people living in foreign countries, including the
billions of persons, the majority of the world population, living in
developing countries. Many Americans have little idea what high drug prices
mean for a country with a per capita income that is one fifth or one tenth
of the United States.
In 2016, the United States had a per capita income of $56,810. Malaysia had
a per capita income of $9,860, just 17 percent of the U.S. Colombia’s per
capita income was $6,310, 11 percent of the U.S. India had a per capita
income of $1,670, less than 3 percent of the U.S. And for the bottom 80
percent of the populations in these countries, things are much worse. If
you target these countries over drug prices, you are going to kill poor
But concern for people living outside the United States is not our only
concern. I live right here. I’m a cancer patient, alive because of an
effective new drug that is extremely expensive. I am in touch with other
cancer patients. We are all living in fear we will lose our insurance, be
forced to pay 20 percent of the cost of drugs, that can cost more than
$150,000 per year, or be denied coverage because a drug is off-label or off
formulary, or because of other real barriers to reimbursement and access.
The United States needs to curb excessive prices on drugs. If you force
every other country to abandon the means of doing so, you lock the United
States into an expensive and unsustainable system that we can’t afford and
which is hurting us more than many will admit.
Knowledge Ecology International
kim.treanor at keionline.org
tel.: +1.202.332.2670 <(202)%20332-2670>
More information about the Ip-health