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Jongbloed W, Scheltens P, Teunissen C. on NEWS: Research Brief: Bead-Based Biomarkers Neatly Divide AD, FTLD, This paper by Irwin at al. raises some important points.
For a study on CSF frontotemporal... 1 May 2012.
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Scheltens P. on NEWS: The EMA Deems Brain Atrophy Valid Trial Selection Measure, I applaud the EMA for taking this, and the previous, initiative, since they clearly may boost... 18 Oct 2011.
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Scheltens P. on PAPER: Burgmans S. et al., 2009, Age and Atrophy: Nothing to Worry About?
In this paper, Burgmans et al. argue that... 29 Sep 2009.
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Scheltens P. on PAPER: Stam CJ. et al., 2007, Recommendation Only. 12 Feb 2007.
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The ALS Forum is a web-based collaborative effort to bring together valuable ALS-related resources for use by researchers worldwide in both academia and industry-based settings.
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Should the FDA be allowed to use data from overseas clinical trials? |
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Absolutely, we are running out of viable subjects in the U.S. |
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Yes, so long as the data is reliable |
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31 |
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No, the trials are not as rigorous |
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3 |
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No, the data should be repeated in the U.S. |
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5 |
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No, the drug sponsors are just trying to cut corners |
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Responses: 51 |
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Archived Polls |
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