3 results on '"Kim Gallagher"'
Search Results
2. Improving Alzheimer's disease phase II clinical trials
- Author
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Michael Gold, Robert M. Berman, Maria C. Carrillo, Kim Gallagher, Eric Siemers, Barry D. Greenberg, J. Michael Ryan, Michael Grundman, and Timothy Ashwood
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Drug ,medicine.medical_specialty ,Epidemiology ,media_common.quotation_subject ,Cost-Benefit Analysis ,Alternative medicine ,Phases of clinical research ,Disease ,Pharmacology ,Cellular and Molecular Neuroscience ,Clinical Trials, Phase II as Topic ,Developmental Neuroscience ,Alzheimer Disease ,medicine ,Humans ,Intensive care medicine ,Pharmaceutical industry ,media_common ,Government ,business.industry ,Health Policy ,Clinical trial ,Psychiatry and Mental health ,Neuroprotective Agents ,Drug development ,Neurology (clinical) ,Geriatrics and Gerontology ,business - Abstract
Over the past 30 years, many drugs have been studied as possible treatments for Alzheimer's disease, but only four have demonstrated sufficient efficacy to be approved as treatments, of which three are in the same class. This lack of success has raised questions both in the pharmaceutical industry and academia about the future of Alzheimer's disease therapy. The high cost and low success rate of drug development across many disease areas can be attributed, in large part, to late-stage clinical failures (Schachter and Ramoni, Nat Rev Drug Discov 2007;6:107–8). Thus, identifying in phase II, or preferably phase I, drugs that are likely to fail would have a dramatic impact on the costs associated with developing new drugs. With this in mind, the Alzheimer's Association convened a Research Roundtable on June 23 and 24, 2011, in Washington, DC, bringing together scientists from academia, industry, and government regulatory agencies to discuss strategies for improving the probability of phase II trial results predicting success when considering the go/no-go decision-making process leading to the initiation of phase III.
- Published
- 2012
3. The Parkinson Progression Marker Initiative (PPMI)
- Author
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Kenneth Marek, Danna Jennings, Shirley Lasch, Andrew Siderowf, Caroline Tanner, Tanya Simuni, Chris Coffey, Karl Kieburtz, Emily Flagg, Sohini Chowdhury, Werner Poewe, Brit Mollenhauer, Paracelsus-Elena Klinik, Todd Sherer, Mark Frasier, Claire Meunier, Alice Rudolph, Cindy Casaceli, John Seibyl, Susan Mendick, Norbert Schuff, Ying Zhang, Arthur Toga, Karen Crawford, Alison Ansbach, Pasquale De Blasio, Michele Piovella, John Trojanowski, Les Shaw, Andrew Singleton, Keith Hawkins, Jamie Eberling, Deborah Brooks, David Russell, Laura Leary, Stewart Factor, Barbara Sommerfeld, Penelope Hogarth, Emily Pighetti, Karen Williams, David Standaert, Stephanie Guthrie, Robert Hauser, Holly Delgado, Joseph Jankovic, Christine Hunter, Matthew Stern, Baochan Tran, Jim Leverenz, Marne Baca, Sam Frank, Cathi-Ann Thomas, Irene Richard, Cheryl Deeley, Linda Rees, Fabienne Sprenger, Elisabeth Lang, Holly Shill, Sanja Obradov, Hubert Fernandez, Adrienna Winters, Daniela Berg, Katharina Gauss, Douglas Galasko, Deborah Fontaine, Zoltan Mari, Melissa Gerstenhaber, David Brooks, Sophie Malloy, Paolo Barone, Katia Longo, Tom Comery, Bernard Ravina, Igor Grachev, Kim Gallagher, Michelle Collins, Katherine L. Widnell, Suzanne Ostrowizki, Paulo Fontoura, Tony Ho, Johan Luthman, Marcel van der Brug, Alastair D. Reith, and Peggy Taylor
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Diagnostic Imaging ,Male ,medicine.medical_specialty ,International Cooperation ,Disease ,Bioinformatics ,Article ,Cohort Studies ,Dopamine transporter imaging ,Humans ,Multicenter Studies as Topic ,Medicine ,Alpha synuclein ,Medical physics ,Web site ,business.industry ,General Neuroscience ,Healthy subjects ,Parkinson Disease ,Biomarker ,Therapeutic trial ,Disease etiology ,Cerebrospinal fluid ,Diffusion tensor imaging ,Disease Progression ,Biomarker (medicine) ,Female ,Observational study ,business ,Neuroscience ,Biomarkers - Abstract
The Parkinson Progression Marker Initiative (PPMI) is a comprehensive observational, international, multi-center study designed to identify PD progression biomarkers both to improve understanding of disease etiology and course and to provide crucial tools to enhance the likelihood of success of PD modifying therapeutic trials. The PPMI cohort will comprise 400 recently diagnosed PD and 200 healthy subjects followed longitudinally for clinical, imaging and biospecimen biomarker assessment using standardized data acquisition protocols at twenty-one clinical sites. All study data will be integrated in the PPMI study database and will be rapidly and publically available through the PPMI web site- www.ppmi-info.org. Biological samples including longitudinal collection of blood, cerebrospinal fluid (CSF) and urine will be available to scientists by application to an independent PPMI biospecimen review committee also through the PPMI web site. PPMI will rely on a partnership of government, PD foundations, industry and academics working cooperatively. This approach is crucial to enhance the potential for success of this ambitious strategy to develop PD progression biomarkers that will accelerate research in disease modifying therapeutics.
- Published
- 2011
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