BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

206 related articles for article (PubMed ID: 23771769)

  • 1. Early benefit assessment (EBA) in Germany: analysing decisions 18 months after introducing the new AMNOG legislation.
    Ruof J; Schwartz FW; Schulenburg JM; Dintsios CM
    Eur J Health Econ; 2014 Jul; 15(6):577-89. PubMed ID: 23771769
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Early benefit assessment of pharmaceuticals in Germany: manufacturers' expectations versus the Federal Joint Committee's decisions.
    Fischer KE; Stargardt T
    Med Decis Making; 2014 Nov; 34(8):1030-47. PubMed ID: 25149822
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Early benefit assessment of new drugs in Germany - results from 2011 to 2012.
    Hörn H; Nink K; McGauran N; Wieseler B
    Health Policy; 2014 Jun; 116(2-3):147-53. PubMed ID: 24472328
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Patient-relevant outcomes and surrogates in the early benefit assessment of drugs: first experiences].
    Kvitkina T; ten Haaf A; Reken S; McGauran N; Wieseler B
    Z Evid Fortbild Qual Gesundhwes; 2014; 108(8-9):528-38. PubMed ID: 25523852
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Analysis of endpoints used in marketing authorisations versus value assessments of oncology medicines in Germany.
    Ruof J; Knoerzer D; Dünne AA; Dintsios CM; Staab T; Schwartz FW
    Health Policy; 2014 Nov; 118(2):242-54. PubMed ID: 25194474
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Evaluation of a possible predictor for Federal Joint Committee decisions on early benefit assessments according to the German act on the reform of the market for medicinal products.
    Schwander B; Banz K; Kaier K; Walzer S
    Health Policy; 2014 Sep; 117(3):334-44. PubMed ID: 25059744
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Inconsistent approaches of the G-BA regarding acceptance of primary study endpoints as being relevant to patients - an analysis of three disease areas: oncological, metabolic, and infectious diseases.
    Staab T; Isbary G; Amelung VE; Ruof J
    BMC Health Serv Res; 2016 Nov; 16(1):651. PubMed ID: 27842592
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Four years of early benefit assessment of new drugs in Germany: a qualitative study on methodological requirements for quality of life data.
    Blome C; Augustin M; Metin H; Lohrberg D
    Eur J Health Econ; 2017 Mar; 18(2):181-193. PubMed ID: 26837412
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Procedures and methods of benefit assessments for medicines in Germany.
    Bekkering GE; Kleijnen J
    Eur J Health Econ; 2008 Nov; 9 Suppl 1():5-29. PubMed ID: 18987905
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Information on new drugs at market entry: retrospective analysis of health technology assessment reports versus regulatory reports, journal publications, and registry reports.
    Köhler M; Haag S; Biester K; Brockhaus AC; McGauran N; Grouven U; Kölsch H; Seay U; Hörn H; Moritz G; Staeck K; Wieseler B
    BMJ; 2015 Feb; 350():h796. PubMed ID: 25722024
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Varying results of early benefit assessment of newly approved pharmaceutical drugs in Germany from 2011 to 2017: A study based on federal joint committee data.
    Peinemann F; Labeit A
    J Evid Based Med; 2019 Feb; 12(1):9-15. PubMed ID: 30701688
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Actual medical care situation and therapeutic needs in multiple sclerosis: Impact of the Pharmaceutical Market Restructuring Act (AMNOG)].
    Bittner S; Meuth SG
    Nervenarzt; 2016 Apr; 87(4):394-401. PubMed ID: 27023842
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Requirements for drug approval and additional benefits assessment: Regulatory aspects and experiences].
    Broich K; Löbker W; Schulte A; Beinlich P; Müller T
    Nervenarzt; 2016 Apr; 87(4):376-85. PubMed ID: 27003322
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Procedures and methods of benefit assessments for medicines in Germany].
    Bekkering GE; Kleijnen J
    Dtsch Med Wochenschr; 2008 Dec; 133 Suppl 7():S225-46. PubMed ID: 19034813
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Drug assessment: IQWiG, G-BA, and an international comparison].
    Glaeske G
    Internist (Berl); 2016 Jan; 57(1):94-101. PubMed ID: 26502888
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Involvement of scientific societies in early benefit assessment: Simulated participation or valuable additional input?].
    Bleß HH; Seidlitz C; Ohlmeier C; de Millas C
    Z Evid Fortbild Qual Gesundhwes; 2018 Feb; 130():49-57. PubMed ID: 29103831
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Methodological approach to determine minor, considerable, and major treatment effects in the early benefit assessment of new drugs.
    Skipka G; Wieseler B; Kaiser T; Thomas S; Bender R; Windeler J; Lange S
    Biom J; 2016 Jan; 58(1):43-58. PubMed ID: 26134089
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Effect of Crossover in Oncology Clinical Trials on Evidence Levels in Early Benefit Assessment in Germany.
    Isbary G; Staab TR; Amelung VE; Dintsios CM; Iking-Konert C; Nesurini SM; Walter M; Ruof J
    Value Health; 2018 Jun; 21(6):698-706. PubMed ID: 29909875
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [The new German drug market law AMNOG from a child and adolescent psychiatry perspective].
    Dittmann RW
    Nervenarzt; 2016 Apr; 87(4):367-75. PubMed ID: 26992908
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Consequences of the German AMNOG for the identification of study objectives to demonstrate clinical efficacy and cost effectiveness of innovative drugs].
    Götte D
    Dtsch Med Wochenschr; 2012 Feb; 137(6):274-80. PubMed ID: 22270904
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.