Alzheimer’s Disease (AD) is a progressive disease that destroys memory and other important mental functions. It is the 6th leading cause of death in the US, and it does not have a cure. The latter fact strongly affects a family of a newly diagnosed with AD patient. Exploring the landscape of ongoing clinical trials, targeting AD, is the next step family takes to assess possible treatment options. clinicaltrials.gov is a database of clinical studies conducted around the world and is a great place to start exploring experimental treatment possibilities. It has user friendly interface and provides extensive amount of clinical trials information. However, it could be overwhelming for someone without special training to dive through tabulated extensive information available at clinicaltrials.gov. A web-based visualization tool, which summaries Alzheimer`s Disease clinal trial information while sourcing data from clinicaltrials.gov, could be a useful tool for those families, impacted by the illness and seeking a quick visual reference guide on AD clinical trials past and present research.
The data were obtained by downloading all results associated with a search for “alzheimer” on the website clinicaltrials.gov. Data were accessed on 11/09/2017. All studies associated with the search term were included regardless of whether the study had previously completed, terminated, or other enrollment status factors. The data used in analyses are available in the Data
file on the github page and the primary datafile used in analysis is called SearchResultsTable.csv
.
Additional variables of interest were obtained by downloading all the data from each webpage associated with all studys returned in the original “alzheimer” search. These data were also accessed on 11/09/2017. Source code for extracting these variables are available in the file Extracting_data_across_all_xml_files.Rmd
also on the github page. An additional dataset called alzheimers_data
containing all variables associated with each study identified during the “alzheimer” search.
The datasets SearchResultsTable.csv
and alzheimers_data
contain largely overlapping variables. The dataset SearchResultsTable.csv
is generally more processed, particularly for natural language variables. However, alzheimers_data
contains several variables not available in SearchResultsTable.csv
that an interested future researcher may access.
The primary datafile (SearchResultsTable.csv
) contained informaton on 1,771 Alzheimer’s disease studies registered with ClinicalTrials.gov. We restricted our analysis on the 928 studies with study sites in the United States, and as of the November 9, 2017 data pull, the earliest clinical trial on Alzheimer’s Disease started on April 01, 1998 and the most recent on September 01, 2017.
We categorized the trials into 5 main categories based on study type and phase:
Observational: if a study is of study type observational (n = 133)
Phase 1/2: if a study is interventional, and phase is classifed as early Phase 1, Phase 1, or combined Phase 1/Phase 2 (n = 436)
Phase 3/4: if a study is interventional, and phase is classified as Phase 3, Phase 4, or combined Phase 3/Phase 4 (n = 204)
Unknown Phase: if a study is interventional, and phase was not specified (n = 155)
Below we present some summary characteristcs of the data with respect to trends in the number of study sites, the number of study funders, and the number of interventions across studies.
Table 1. Descriptive statistics by study type | ||||
Study Type | ||||
---|---|---|---|---|
Observational | Phase 1/Phase 2 | Phase 3/Phase 4 | Unknown Phase | |
No. Study Sites | ||||
Mean | 7.0 | 10.7 | 55.6 | 4.1 |
Std. dev. | 19.8 | 20.2 | 73.6 | 21.2 |
Median | 1.0 | 1.0 | 24.0 | 1.0 |
Min. | 1.0 | 1.0 | 1.0 | 1.0 |
Max. | 145.0 | 142.0 | 348.0 | 249.0 |
No. Funders | ||||
Mean | 1.4 | 1.2 | 1.3 | 1.4 |
Std. dev. | 0.5 | 0.4 | 0.5 | 0.5 |
Median | 1.0 | 1.0 | 1.0 | 1.0 |
Min. | 1.0 | 1.0 | 1.0 | 1.0 |
Max. | 3.0 | 3.0 | 3.0 | 3.0 |
No. Interventions | ||||
Mean | 1.6 | 1.9 | 1.8 | 1.9 |
Std. dev. | 1.0 | 1.0 | 0.9 | 1.1 |
Median | 1.0 | 2.0 | 2.0 | 2.0 |
Min. | 1.0 | 1.0 | 1.0 | 1.0 |
Max. | 6.0 | 6.0 | 6.0 | 8.0 |
We also examined the number of new studies each year. Figure 1 shows that there were peaks in the number of new studies in 2009 and 2016. If we look closely in Figure 2, we can see that the spike in 2009 is due to the large increase in Phase 1 and/or Phase 2 studies, which is indicative of a large number of new treatments being investigated. This happened because major pharmaceutical efforts were concentrated around finding a cure for Alzheimer`s Disease with promising drug candidates in pipeline. The spike in 2016, however, appears to be due to the combination of increased unclassified (in terms of study phase) trials, and a relatively high number of Phase 1/2 trials.
In the exploratory data interface, we present three interactive plots that will allow the user to subset and explore the data. We offer an interactive Gantt chart that allows the user to visualize trends in study length and interactive line plots were created the help the user visualize trends in age ranges of targeted participants.
Finally, we provide an interactive map that allows users to get a sense for how study locations are distributed across the US.
The Shiny dashboard created in this project creates a simple and user-friendly format for interested parties including physician and researchers with less statistical and the data savy patient to explore trends in Alzheimer`s-related clinical trials. We encourage the user to explore these interactive plots and also to download the source data from our github page and continue deriving insights into trends in Alzheimber’s studies!
Below we provide the full dataset used for this project, so that users can further examine the data associated with paraticular studies without having to download the full dataset from github.
Possible future directions for this project include updating the Shiny dashboard so that it interacts in real time with the clinicaltrials.gov website. This would allow the data in the dashboard to continue to provide the most up to date information to the user, and would prevent the dashboard from becoming obsolete over time.
Other possible future directions include incorporating additional variables so that the user can gain a more complete picture of the avialable data. Another area of possible expansion might include developing a platform for the user to perform simple statistical tests on the data from within the project website.
rank | nct_number | title | acronym | recruitment | study_results | conditions | interventions | outcome_measures | sponsor_collaborators | gender | age | phases | enrollment | funded_bys | study_type | study_designs | other_ids | start_date | primary_completion_date | completion_date | last_verified | first_submitted | first_posted | results_first_submitted | results_first_posted | last_update_submitted | last_update_posted | locations | url |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
3 | NCT00076440 | Antigonadotropin-Leuprolide in Alzheimer's Disease Drug INvestigation (ALADDIN) VP 104 Study | null | Completed | No Results Available | Alzheimer Disease | Drug: Leuprolide acetate | Voyager Pharmaceutical Corporation|National Institute on Aging (NIA) | Male | 65 Years and older (Adult, Senior) | Phase 2 | 90 | Industry | Interventional | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Double|Primary Purpose: Treatment | IA0051 | December 2003 | March 2007 | March 2007 | March 2007 | January 22, 2004 | January 26, 2004 | null | null | December 10, 2009 | December 11, 2009 | Margolin Brain Institute, Fresno, California, United States|Bay Area Research Institute, Lafayette, California, United States|Southwest Clinical Research, Rancho Mirage, California, United States|Geriatric and Adult Psychiatry LLC, Hamden, Connecticut, United States|Baumel-Eisner Neuromedical Institute, Boca Raton, Florida, United States|Brain Matters Research, Delray Beach, Florida, United States|Baumel-Eisner Neuromedical Institute, Ft. Lauderdale, Florida, United States|Baumel-Eisner Neuromedical Institute, Miami Beach, Florida, United States|Meridien Research, St. Petersburg, Florida, United States|Boston University School of Medicine, Boston, Massachusetts, United States|Medical University of South Carolina, Charleston, South Carolina, United States|Innovative Clinical Research Center, Alexandria, Virginia, United States|Middleton VA Wisconsin Alzheimer's Institute, Madison, Wisconsin, United States | https://ClinicalTrials.gov/show/NCT00076440 | |
4 | NCT01867372 | Early Markers of Alzheimer's Disease: Structural and Functional Brain Changes | null | Terminated | No Results Available | Alzheimer's Disease | Accelerated preclinical changes in brain structure and function in specific regions will predict which individuals develop cognitive impairment and Alzheimer s disease|Changes in brain structure are predictors of cognitive decline and impairment though neuroimaging assessments | National Institute on Aging (NIA)|Johns Hopkins University|National Institutes of Health Clinical Center (CC) | All | 20 Years and older (Adult, Senior) | 300 | NIH|Other | Observational | Time Perspective: Other | 999903328|03-AG-N328 | March 10, 2003 | September 22, 2014 | September 22, 2014 | September 22, 2014 | May 30, 2013 | June 4, 2013 | null | null | July 6, 2017 | July 7, 2017 | Johns Hopkins University, Baltimore, Maryland, United States|Kennedy Krieger Institute, Baltimore, Maryland, United States|National Institute of Aging, Clinical Research Unit, Baltimore, Maryland, United States | https://ClinicalTrials.gov/show/NCT01867372 | ||
6 | NCT00088673 | Evaluation of 3APS in Patients With Mild to Moderate Alzheimer’s Disease | null | Unknown status | No Results Available | Alzheimer Disease | Drug: 3APS | The two primary efficacy parameters are the change from baseline to month 18 in the Alzheimer's Disease Assessment Scale, cognitive subpart (ADAS-cog) and the clinical Deterioration Scale Sum of Boxes (CDR-SB) scores.|The brain volume change from baseline as measured by Magnetic Resonance Imaging will also be assessed. | Bellus Health Inc | All | 50 Years and older (Adult, Senior) | Phase 3 | 950 | Industry | Interventional | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Double|Primary Purpose: Treatment | CL-758007 | June 2004 | null | null | February 2007 | July 30, 2004 | August 3, 2004 | null | null | February 27, 2007 | February 28, 2007 | Pivotal Research Centers, Peoria, Arizona, United States|21st Century Neurology, a division of Xenoscience, Phoenix, Arizona, United States|Central Arkansas Research, Hot Springs, Arkansas, United States|Margolin Brain Institute, Fresno, California, United States|Senior Clinical Trials, Inc., Laguna Hills, California, United States|Pacific Research Network, Inc., San Diego, California, United States|San Francisco Clinical Research Center, San Francisco, California, United States|Radiant Research, Denver, Colorado, United States|Research Center for Clinical Studies, Inc., Darien, Connecticut, United States|Yale University, Alzheimer's Disesase Research Unit, New Haven, Connecticut, United States|New England Research Institute, Stamford, Connecticut, United States|Georgetown University Medical Center, Washington, District of Columbia, United States|Neuropsychiatric Research Center of SouthWest Florida, Fort Myers, Florida, United States|Berma Research Group, Hialeah, Florida, United States|Tukoi Institute for Clinical Research, Miami, Florida, United States|Palm Beach Neurological Center, Palm Beach Gardens, Florida, United States|Quantum Laboratories Inc at the Memory Disorders Clinic, North Broward Medical Center, Pompano Beach, Florida, United States|Axiom Clinical Research, Tampa, Florida, United States|Byrd Alzheimer’s Center and Research Institute, Tampa, Florida, United States|Stedman Clinical Trials, Tampa, Florida, United States|University of South Florida, Suncoast Gerontology Center, Tampa, Florida, United States|Premiere Research Institute Palm Beach Neurology, West Palm Beach, Florida, United States|Comprehensive Neurology Specialists, PC, Atlanta, Georgia, United States|Emory University, Atlanta, Georgia, United States|Southern Illinois University (SIU) School of Medicine, Department of Neurology, Springfield, Illinois, United States|Brigham & Women's Hospital, Boston, Massachusetts, United States|Mood & Memory Clinic - Dr Aronson, Farmington Hills, Michigan, United States|Memory Enhancement Center, Long Branch, New Jersey, United States|Neurological Associates of Albany, Albany, New York, United States|Eastside Comprehensive Medical Center, New York, New York, United States|NYU School of Medicine, New York, New York, United States|Global Research and Consulting, Olean, New York, United States|Nathan S. Kline Institute, Orangeburg, New York, United States|University of Rochester-Program in Neurobehavioral Therapeutics, Rochester, New York, United States|Richard H. Weisler, MD, PA and Associates, Raleigh, North Carolina, United States|Wake Forest University School of Medicine, Department of Psychiatry and Behavioral Medicine, Winston-Salem, North Carolina, United States|University Memory and Aging Center, Cleveland, Ohio, United States|Neurology and Neuroscience Center of Ohio, Toledo, Ohio, United States|Clinical Pharmaceuticals Trials, Inc., Tulsa, Oklahoma, United States|CNS Research Institute, Philadelphia, Pennsylvania, United States|Farber Institute for Neurosciences, Philadelphia, Pennsylvania, United States|University of Pennsylvania, Philadelphia, Pennsylvania, United States|University of Pittsburgh ADRC, Pittsburgh, Pennsylvania, United States|CNS Research, Inc., East Providence, Rhode Island, United States|Memory and Aging Program, Butler Hospital, Providence, Rhode Island, United States|MUSC - Alzheimer's Research and Clinical Programs, North Charleston, South Carolina, United States|Clinical Research Services at Tennessee Christian Medical Center, Madison, Tennessee, United States|University of Texas Mental Sciences Institute, Houston, Texas, United States|Air Force Villages-Freedom House Research (Study open to Air Force Village residents only), San Antonio, Texas, United States|The Memory Clinic, Bennington, Vermont, United States|Calgary, Alberta, Canada|The Medical Arts Health Research Group, a Division of PCT Networks, Inc., Penticton, British Columbia, Canada|St. Joseph's Hospital, Saint-John, New Brunswick, Canada|Queen Elizabeth II Health Sciences Centre, Halifax, Nova Scotia, Canada|Queen's University, Kingston, Ontario, Canada|Geriatric Clinical Trials Group, Parkwood Hospital, London, Ontario, Canada|Ottawa, Ontario, Canada|Gerontion Research, Toronto, Ontario, Canada|Sunnybrook and Women's College Health Science Centre, Toronto, Ontario, Canada|Toronto Memory Program, Toronto, Ontario, Canada|Clinique Neuro Rive-Sud, Greenfield Park, Quebec, Canada|Hôpital Maisonneuve-Rosemont, Recherche Clinique de Neurologie, Montreal, Quebec, Canada|Jewish General Hospital- Memory Clinic, Montreal, Quebec, Canada|Centre de recherche Novabyss, Sherbrooke, Quebec, Canada|McGill Centre for Studies in Aging, Verdun (Montreal), Quebec, Canada|Hôpital de l'Enfant-Jésus, Ville de Quebec, Quebec, Canada|Memory & Motor Skills Disorders Clinic, Ville de Québec, Quebec, Canada | https://ClinicalTrials.gov/show/NCT00088673 |
7 | NCT00051909 | Efficacy and Safety of LY451395 in Patients With Probable Alzheimer's Disease | null | Completed | No Results Available | Alzheimer's Disease | Drug: LY451395 | Eli Lilly and Company | All | 50 Years and older (Adult, Senior) | Phase 2 | 200 | Industry | Interventional | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Double|Primary Purpose: Treatment | 6764|H6N-MC-LEAM | November 2002 | null | June 2003 | July 2006 | January 17, 2003 | January 20, 2003 | null | null | July 18, 2006 | July 19, 2006 | Beverly Hills, California, United States|Fresno, California, United States|Boca Raton, Florida, United States|Fort Lauderdale, Florida, United States|Miami Beach, Florida, United States|Boston, Massachusetts, United States|Oklahoma City, Oklahoma, United States|Tulsa, Oklahoma, United States|Wichita Falls, Texas, United States | https://ClinicalTrials.gov/show/NCT00051909 | |
8 | NCT00007189 | Alzheimer's Disease Anti-Inflammatory Prevention Trial (ADAPT) | null | Completed | No Results Available | Alzheimer Disease | Drug: Naproxen Sodium (Aleve)|Drug: Celecoxib (Celebrex) | Seattle Institute for Biomedical and Clinical Research|National Institute on Aging (NIA)|VA Puget Sound Health Care System|University of Washington|Johns Hopkins University | All | 70 Years and older (Senior) | Phase 3 | 2625 | Other|NIH|U.S. Fed | Interventional | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Double|Primary Purpose: Prevention | IA0026|U01AG015477 | January 2001 | May 2007 | null | October 2016 | December 14, 2000 | December 14, 2000 | null | null | October 18, 2016 | October 19, 2016 | Sun Health Research Institute, Sun City, Arizona, United States|Roskamp Institute Memory Clinic, 10770 N. 46th Street, Tampa, Florida, United States|Johns Hopkins University, Baltimore, Maryland, United States|Boston University School of Medicine, Boston, Massachusetts, United States|University of Rochester, Rochester, New York, United States|Veterans Affairs Puget Sound Health Care System, University of Washington, Seattle, Washington, United States | https://ClinicalTrials.gov/show/NCT00007189 | |
10 | NCT00100334 | Safety Study of PPI-1019 in Subjects With Mild-Moderate Alzheimer’s Disease | null | Completed | No Results Available | Alzheimer's Disease | Drug: PPI-1019 (APAN) | Safety will be assessed through the occurrence of clinical adverse events and the occurrence of clinically significant changes from baseline. | PRAECIS Pharmaceuticals Inc. | All | 50 Years to 80 Years (Adult, Senior) | Phase 1|Phase 2 | 24 | Industry | Interventional | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Double|Primary Purpose: Treatment | 1019-04-01 | December 2004 | null | August 2005 | September 2006 | December 29, 2004 | December 30, 2004 | null | null | September 18, 2006 | September 19, 2006 | Silverado Senior Living, San Juan Capistrano, California, United States | https://ClinicalTrials.gov/show/NCT00100334 |
11 | NCT00762411 | Effects of LY450139, on the Progression of Alzheimer's Disease as Compared With Placebo | IDENTITY-2 | Completed | Has Results | Alzheimer's Disease | Drug: LY450139|Drug: Placebo | Change From Baseline in Alzheimer's Disease Assessment Scale- Cognitive Subscale (ADAS-Cog11) at 76 Weeks|Change From Baseline in Alzheimer's Disease Assessment Scale- Cognitive Subscale (ADAS-Cog11) at 16 Weeks After Cessation of Study Drug|Change From Baseline in Alzheimer's Disease Cooperative Study Activities of Daily Living Inventory (ADCS-ADL) at 76 Weeks|Change From Baseline in Alzheimer's Disease Cooperative Study Activities of Daily Living Inventory (ADCS-ADL) at 16 Weeks After Cessation of Study Drug|Change From Baseline in Clinical Dementia Rating Sum of Boxes (CDR-SB) at 76 Weeks|Change From Baseline in Neuropsychiatric Inventory (NPI) at 76 Weeks|Change From Baseline in the Resource Utilization in Dementia-Lite (RUD-Lite) up to 76 Weeks|Change From Baseline in the EuroQol 5-Dimensional Health-Related Quality of Life Scale Proxy Version (EQ-5D Proxy) Visual Analog Scale (VAS) at 76 Weeks|Change From Baseline in Quality of Life in Alzheimer's Disease (QoL-AD) at 76 Weeks|Change From Baseline in Mini Mental State Examination (MMSE) at 76 Weeks|Percent Change From Baseline in Amyloid Beta (Aβ) 1-42 Plasma Concentration at 52 Weeks|Change From Baseline in Positron Emission Tomography (PET) Using Fluorine-18 Fluorodeoxyglucose (18F-FDG) at 76 Weeks|Change From Baseline in Hippocampal Volume Using Volumetric Magnetic Resonance Imaging (vMRI) up to 76 Weeks|Change From Baseline in Amyloid Imaging Positron Emission Tomography (AV-45 PET) up to 76 Weeks|Change From Baseline in Tau Concentration in Spinal Fluid up to 76 Weeks|LY450139 Population Pharmacokinetics: Clearance of LY450139|LY450139 Population Pharmacokinetics: Volume of Distribution of LY450139|Change From Baseline in Clinical Dementia Rating Sum of Boxes (CDR-SB) at 4 Weeks After Cessation of Study Drug|Change From Baseline in Neuropsychiatric Inventory (NPI) at 4 Weeks After Cessation of Study Drug|Change From Baseline in Resource Utilization in Dementia-Lite (RUD-Lite) at 4 Weeks After Cessation of Study Drug|Change From Baseline in EuroQol 5-Dimensional Health-Related Quality of Life Scale Proxy Version (EQ-5D Proxy) Visual Analog Scale (VAS) at 4 Weeks After Cessation of Study Drug|Change From Baseline in Quality of Life in Alzheimer's Disease (QoL-AD) at 4 Weeks After Cessation of Study Drug|Change From Baseline in Mini Mental State Examination (MMSE) 4 Weeks After Cessation of Study Drug|Change From Baseline in Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS-Cog12) at 76 Weeks|Change From Baseline in Alzheimer's Disease Assessment Scale (ADAS-Cog14) at 76 Weeks|Change From Baseline in Phosphorylated-Tau (P-tau) Concentration in Spinal Fluid up to 76 Weeks|Change From Baseline in Amyloid Beta (Aβ) 1-42 Concentration in Spinal Fluid up to 76 Weeks|Change From Baseline in Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS-Cog12) at 16 Weeks After Cessation of Study Drug|Change From Baseline in Alzheimer's Disease Assessment Scale (ADAS-Cog14) at 16 Weeks After Cessation of Study Drug | Eli Lilly and Company | All | 55 Years and older (Adult, Senior) | Phase 3 | 1111 | Industry | Interventional | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|Primary Purpose: Treatment | 11271|H6L-MC-LFBC | September 2008 | April 2011 | April 2011 | January 2015 | September 26, 2008 | September 30, 2008 | November 6, 2013 | September 25, 2014 | January 28, 2015 | February 16, 2015 | For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Phoenix, Arizona, United States|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Costa Mesa, California, United States|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., La Jolla, California, United States|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Laguna Hills, California, United States|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Los Angeles, California, United States|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Oxnard, California, United States|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., San Francisco, California, United States|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Boca Raton, Florida, United States|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Hallandale Beach, Florida, United States|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Hollywood, Florida, United States|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Miami, Florida, United States|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Orlando, Florida, United States|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Tampa, Florida, United States|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., New Orleans, Louisiana, United States|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Shreveport, Louisiana, United States|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Hattiesburg, Mississippi, United States|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Omaha, Nebraska, United States|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Albany, New York, United States|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Manhasset, New York, United States|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Durham, North Carolina, United States|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Oklahoma City, Oklahoma, United States|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Philadelphia, Pennsylvania, United States|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Rio De Janeiro, Brazil|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Salvador, Brazil|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., São Paulo, Brazil|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Sofia, Bulgaria|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Winnipeg, Manitoba, Canada|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Saint John, New Brunswick, Canada|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., London, Ontario, Canada|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Ottawa, Ontario, Canada|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Peterborough, Ontario, Canada|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Toronto, Ontario, Canada|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Greenfield Park, Quebec, Canada|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Montreal, Quebec, Canada|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Verdun, Quebec, Canada|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Beijing, China|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Shanghai, China|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Xi'An, China|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Montpellier, France|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Paris, France|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Poitiers, France|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Strasbourg, France|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Berlin, Germany|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Frankfurt, Germany|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Hamburg, Germany|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Heidelberg, Germany|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Mannheim, Germany|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Budapest, Hungary|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Esztergom, Hungary|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Boggiovara, Italy|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Cassino, Italy|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Milano, Italy|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Parma, Italy|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Akita, Japan|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Fukuoka, Japan|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Hyogo, Japan|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Ibaraki, Japan|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Iwate, Japan|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Kanagawa, Japan|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Kumamoto, Japan|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Kyoto, Japan|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Nagasaki, Japan|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Osaka, Japan|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Saitama, Japan|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Tokyo, Japan|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Seoul, Korea, Republic of|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Suwon, Korea, Republic of|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Aguascalientes, Mexico|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Monterrey, Mexico|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Saltillo, Mexico|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Bucharest, Romania|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Timisoara, Romania|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Ekaterinburg, Russian Federation|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Kazan, Russian Federation|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Saint Petersburg, Russian Federation|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Saratov, Russian Federation|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Belgrade, Serbia|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Kragujevac, Serbia|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Changhua, Taiwan|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Tainan, Taiwan|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Taipei, Taiwan|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Tao-Yuan, Taiwan|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Eskisehir, Turkey|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Istanbul, Turkey|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Izmir, Turkey|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Samsun, Turkey|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Dnipropetrovsk, Ukraine|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Donetsk, Ukraine|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Kherson, Ukraine|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Kyiv, Ukraine|For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Odesa, Ukraine | https://ClinicalTrials.gov/show/NCT00762411 |
17 | NCT00870519 | Brain Imaging Study in Subjects With Alzheimer Disease in Comparison to Healthy Subjects | null | Terminated | No Results Available | Alzheimer's Disease | Drug: I-123-MNI-168|Drug: 123-I MNI-168 | To assess the uptake and washout of {I123}MNI-168, a potential imaging biomarker for β-amyloid burden in brain,|To acquire initial safety data following injection of (123I) MNI-168. | Institute for Neurodegenerative Disorders | All | 50 Years and older (Adult, Senior) | Phase 1 | 2 | Other | Interventional | Allocation: Non-Randomized|Intervention Model: Parallel Assignment|Masking: None (Open Label)|Primary Purpose: Diagnostic | MNI-168-01 | January 2009 | January 2010 | January 2011 | February 2011 | March 26, 2009 | March 27, 2009 | null | null | February 24, 2011 | February 25, 2011 | Institute for Neurodegenerative Disorders, New Haven, Connecticut, United States | https://ClinicalTrials.gov/show/NCT00870519 |
20 | NCT01703117 | Riluzole in Mild Alzheimer's Disease | null | Recruiting | No Results Available | Alzheimer's Disease | Drug: Riluzole|Drug: Placebo | Imaging Biomarkers N-acetylaspartate (NAA) and FDG-PET values in regions of interest|Cognitive function (neuropsychological tests); Glutamate levels obtained through MRS | Rockefeller University | All | 60 Years to 85 Years (Adult, Senior) | Phase 2 | 48 | Other | Interventional | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Double (Participant, Investigator)|Primary Purpose: Treatment | APE-0792 | November 2013 | November 2019 | November 2019 | September 2017 | October 4, 2012 | October 10, 2012 | null | null | September 21, 2017 | September 25, 2017 | The Rockefeller University, New York, New York, United States | https://ClinicalTrials.gov/show/NCT01703117 |
22 | NCT01254448 | Multiple Ascending Dose Study of TC-5619 in Healthy Elderly Subjects and Subjects With Alzheimer's Disease | null | Completed | No Results Available | Alzheimer's Disease | Drug: TC-5619|Drug: Placebo | Number of Participants with Adverse Events as a Measure of Safety and Tolerability|Pharmacokinetic profiles|Markers of inflammation in cerebrospinal fluid|Markers of inflammation in plasma | Targacept Inc. | All | 55 Years to 80 Years (Adult, Senior) | Phase 1 | 38 | Industry | Interventional | Allocation: Randomized|Intervention Model: Single Group Assignment|Masking: Triple (Participant, Care Provider, Investigator)|Primary Purpose: Diagnostic | TC-5619-238-CLP-003 | September 2010 | March 2011 | May 2011 | September 2013 | December 2, 2010 | December 6, 2010 | null | null | September 3, 2013 | September 4, 2013 | Collaborative Neuroscience Network, Long Beach, California, United States|San Francisco Clinical Research Center, San Francisco, California, United States|MD Clinical, Hallandale Beach, Florida, United States|Galiz Research, Miami Springs, Florida, United States|Comprehensive Phase One, Miramar, Florida, United States|Compass Research, LLC, Orlando, Florida, United States|Atlanta Center For Clinical Research, Atlanta, Georgia, United States|Princeton Medical Institutes, Princeton, New Jersey, United States|Community Clinical Research, Austin, Texas, United States|Aspen Clinical Research, Orem, Utah, United States | https://ClinicalTrials.gov/show/NCT01254448 |