Surrogate Biomarkers
Author:
Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-030-31503-0_3
Reference32 articles.
1. DiMasi, J. A., Grabowski, H. G., & Hansen, R. W. (2016). Innovation in the pharmaceutical industry: new estimates of R&D costs. Journal of health economics, 47, 20–33.
2. Paul, S. M., Mytelka, D. S., Dunwiddie, C. T., Persinger, C. C., Munos, B. H., Lindborg, S. R., & Schacht, A. L. (2010). How to improve R&D productivity: the pharmaceutical industry’s grand challenge. Nature reviews Drug discovery, 9(3), 203.
3. Burzykowski, T., Molenberghs, G., & Buyse, M. (2005). The Evaluation of Surrogate Endpoints. Springer.
4. Buyse, M. and Molenberghs, G. (1998). Criteria for the validation of surrogate endpoints in randomized experiments. Biometrics, 54:1014–1029.
5. Buyse, M., Molenberghs, G., Burzykowski, T., Renard, D., & Geys, H. (2000). The validation of surrogate endpoints in meta-analyses of randomized experiments. Biostatistics, 1(1), 49–67.
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