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Ticagrelor: Considerable added benefit for specific patients
Date:10/11/2011

dossiers by IQWiG. Because of time limitations, this is mostly done by post. Medical advisors, generally specialists, and representatives of affected patients are sent questionnaires. This allows them to provide information about what they consider to be the important points for the treatment of the specific disease.

Practicable and transparent procedure

At the end of September 2011, IQWiG transmitted the dossier assessment to the G-BA, which then published it on 4 October 2011 - together with the manufacturer's dossier - and initiated the commenting procedure. It is planned that the G-BA will complete the assessment within three months of the publication. According to Thomas Kaiser, Head of the Department of Drug Assessment: "It is a real milestone, also internationally, that not only the IQWiG assessment is being published, but that the manufacturer has to disclose all relevant data. This is one reason why international experts are so interested in the early benefit assessment."

In IQWiG's opinion, the AMNOG procedure has passed its first practical test. Jrgen Windeler summarizes: "It is practicable and can be implemented in detail. The legal specifications have turned out to be appropriate. The first assessment certified that the drug shows added benefit and this demonstrates that the anxieties which have been expressed again and again by the pharmaceutical industry are unjustified. AMNOG does not present a threat to Germany as a site for industry."


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Contact: Anna-Sabine Ernst
presse@iqwig.de
49-221-356-850
Institute for Quality and Efficiency in Health Care
Source:Eurekalert

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