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Multi-dimensional capture of patient-relevant endpoints in regulatory trials and health technology assessments in oncology two years after introduction of the German AMNOG health care reform

Dintsios, C.; Knoerzer, D.; Dünne, A.; Schwartz, F.; Ruof, J. · Das Gesundheitswesen · Ausgabe 8/09/2013 · S. 1 bis 1

DOI 10.1055/s-0033-1354237

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Autor:innenDintsios, C.; Knoerzer, D.; Dünne, A.; Schwartz, F.; Ruof, J.
ZeitschriftDas Gesundheitswesen
Ausgabe8/09/2013
Jahrgang / SeitenJg. 75 · S. 1 bis 1

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Abstract-Vorschau

Objectives: With the introduction of AMNOG in January 2011, an early benefit assessment (EBA) was required for new medicines in Germany. EBAs are based on the additional therapeutic benefit of a drug on patient-relevant endpoints (PREs). We compared the acceptance of PREs for oncology in regulatory trials, and in EBAs conducted by German health technology assessment (HTA) bodies. Methods: EBAs on oncology drugs and…

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Zitierempfehlung

Dintsios, C.; Knoerzer, D.; Dünne, A.; Schwartz, F.; Ruof, J (2013) Multi-dimensional capture of patient-relevant endpoints in regulatory trials and health technology assessments in oncology two years after introduction of the German AMNOG health care reform. Das Gesundheitswesen, 75 (8/09), 1 bis 1. https://doi.org/10.1055/s-0033-1354237

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