Dear All,
further to my previous post on the confidentiality of prices in Germany after IQWIG assessment it seems that an agreement of confidentiality could not be reached and it looks like that rebate prices are being published.
If that is the case profound implication on European prices can be expected through external price referencing.
Here is a link to a presentation I gave on the topic
Regards
Ulf
7.11.2012
New Tufts study on oncology market access
July 10, 2012
U.S. Cancer Patients Get Faster Access to More Oncology Drugs than European Patients
BOSTON — July 10, 2012 — Cancer patients in the United States get faster access to more oncology drugs to treat their disease than patients in Europe, according to a newly completed study by the Tufts Center for the Study of Drug Development.
In addition, the study found, new oncology drug approvals in the U.S. outpaced European approvals by 33% between 2000 and 2011.
“While greater access to more treatment options is definitely a positive for patients in the U.S., it is not clear if greater access leads to better health outcomes,” noted Joshua P. Cohen, research assistant professor at Tufts CSDD who conducted the analysis.
He said that the growing use of comparative effectiveness research, which provides information on the relative strengths and weaknesses of different medical technologies, could help close the gap between what is known and what is done in pharmaceutical care.
“Although more oncology drugs are available in the U.S., and the costs for a higher share of them are reimbursed, the evidence-based approach adopted by European systems have improved the affordability of drugs in Europe that are considered to be cost-effective,” Cohen said.
The study, reported in the July/August Tufts CSDD Impact Report and released today, also found that:
*Between 2000 and 2011, 40 oncology drugs received market approval in the U.S. compared to 30 in Europe.
*Oncology drug prices in Europe, on average, are 9% lower than in the U.S.
*Patient cost sharing is much lower in Europe than the U.S., where the average co-insurance rate per covered drug is 33%.
About the Tufts Center for the Study of Drug Development
The Tufts Center for the Study of Drug Development (http://csdd.tufts.edu) at Tufts University provides strategic information to help drug developers, regulators, and policy makers improve the quality and efficiency of pharmaceutical development, review, and utilization. Tufts CSDD, based in Boston, conducts a wide range of in-depth analyses on pharmaceutical issues and hosts symposia, workshops, and public forums, and publishes Tufts CSDD Impact Reports, a bi-monthly newsletter providing analysis and insight into critical drug development issues.
—end—
Contacts: Tufts Center for the Study of Drug Development
Sandra Peters — 617-636-2185
sandra.peters@tufts.edu
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