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1 to 4 of 4 results |
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Relkin N. on NEWS: Gammagard™ Misses Endpoints in Phase 3 Trial, The topline results were announced today to satisfy SEC requirements and Baxter's obligation to... 8 May 2013.
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Relkin N. on NEWS: Quick-and-Early IVIG Therapy: Hints of Promise, First off, I’d like to disclose that I am lead investigator in the GAP 160701 Study, which is... 29 Mar 2013.
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Relkin N, Szabo P. on PAPER: Dodel R. et al., 2011, It is gratifying to see a consensus emerging about the existence of naturally occurring... 27 Apr 2011.
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Lee K, Relkin N. on PAPER: Finehout EJ. et al., 2007, The stringent requirements for a diagnosis of definite Alzheimer disease (AD) make it unlikely... 8 Jan 2007.
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1 to 4 of 4 results |
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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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 Antibodies
Cell Lines
Collaborators
Papers
Research Participants
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