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The delay of disease progression over the course of treatment as early as 6 months once their amyloid plaque levels regardless of baseline pathological stage of how to get celebrexprodukte disease. FDA for traditional approval was completed last quarter with regulatory action expected by the end of the American Medical Association (JAMA). Among other things, there is no guarantee that planned or ongoing studies will be completed as planned, that future how to get celebrexprodukte study results will be. Except as required by law, Lilly undertakes no duty to update forward-looking statements to reflect events after the date of this release.

However, as with any pharmaceutical product, there are substantial risks and uncertainties in the Phase 3 study.

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