CDC/NIH Workshop. Tuberculosis biomarker and surrogate endpoint research roadmap
- PMID: 21737585
- PMCID: PMC3208659
- DOI: 10.1164/rccm.201105-0827WS
CDC/NIH Workshop. Tuberculosis biomarker and surrogate endpoint research roadmap
Abstract
The Centers for Disease Control and Prevention and National Institutes of Health convened a multidisciplinary meeting to discuss surrogate markers of treatment response in tuberculosis. The goals were to assess recent surrogate marker research and to provide specific recommendations for (1) the qualification and validation of biomarkers of treatment outcome; (2) the standardization of specimen and data collection for future clinical trials, including a minimum set of samples and collection time points; and (3) the creation ofa specimen repository to support biomarker testing. This article summarizes these recommendations and provides a roadmap for their implementation.
Figures
References
-
- Ma Z, Lienhardt C, McIlleron H, Nunn AJ, Wang X. Global tuberculosis drug development pipeline: the need and the reality. Lancet 2010;375:2100–2109 - PubMed
-
- Spigelman M, Gillespie S. Tuberculosis drug development pipeline: progress and hope. Lancet 2006;367:945–947 - PubMed
-
- Jindani A, Dore CJ, Mitchison DA. Bactericidal and sterilizing activities of antituberculosis drugs during the first 14 days. Am J Respir Crit Care Med 2003;167:1348–1354 - PubMed
-
- Nuermberger E. Using animal models to develop new treatments for tuberculosis. Semin Respir Crit Care Med 2008;29:542–551 - PubMed
-
- Davies GR, Phillips PP, Nunn AJ. Biomarkers and surrogate end points in clinical trials of tuberculosis treatment. J Infect Dis 2007;196:648–649, author reply 649–650 - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
