[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"trial:NCT04786223":3,"trial-entities:NCT04786223":98,"trial-summary:NCT04786223":104},{"id":4,"nct_id":4,"org_study_id":5,"brief_title":6,"official_title":6,"overall_status":7,"completion_date":8,"status_verified_date":9,"last_update_date":10,"start_date":11,"sponsor_name":12,"lead_sponsor_class":13,"has_dmc":14,"brief_summary":15,"detailed_description":16,"conditions":17,"keywords":20,"study_type":23,"primary_purpose":24,"phases":25,"enrollment_info":27,"interventions":30,"primary_outcomes":42,"secondary_outcomes":53,"sex":58,"minimum_age":59,"maximum_age":60,"healthy_volunteers":14,"eligibility_criteria":61,"std_ages":74,"locations":77,"central_contacts":87,"overall_officials":88,"references":93,"see_also_links":94},"NCT04786223","20-000866","Targeting Neuroinflammation as a Contributing Pathology in Alzheimer's Disease Dementia and Related Dementias","ENROLLING_BY_INVITATION","2030-03","2026-05","2026-05-22","2021-03-30","Val Lowe","OTHER",true,"This study is being done to research the usefulness of PET\u002FCT imaging for measuring brain inflammation and its relation to Alzheimer's Disease Dementia and related dementias. Additionally, researchers are looking to learn more about the side effects of a new radioactive tracer (radiotracer) C-11 ER176.","Alzheimer's disease (AD) dementia is a devastating illness with no cure. Treatments targeting known pathologic hallmarks of AD, such as amyloid-beta (AB), in symptomatic individuals have proved largely fruitless so other potential disease targets warrant exploration. Neuroinflammation has interesting possible associations with AD dementia and may contribute to AD dementia in different ways among different individuals. Previous PET neuroinflammation data are not entirely consistent and new methods of PET imaging and studies with larger cohorts are needed to further investigate the role of neuroinflammation in AD dementia and the utility of PET as a biomarker. This project seeks to test new PET neuroinflammation imaging methods in unimpaired, mildly impaired, AD dementia, and mild cognitively impaired and dementia with Lewy bodies (DLB) individuals with biomarker-identified brain pathology to help address these gaps in knowledge in the field.",[18,19],"Lewy Body Dementia (LBD)","Alzheimer Dementia (AD)",[21,22],"ER176","Neuroinflammation","INTERVENTIONAL","DIAGNOSTIC",[26],"PHASE2",{"count":28,"type":29},125,"ESTIMATED",[31,37],{"type":32,"name":33,"description":34,"armGroupLabels":35},"DRUG","C-11 ER-176","Participants will receive a one-time administration of C-11 ER176 and undergo a PET\u002FCT imaging study. Participants may be invited to return for an additional administration of C-11 ER176 and undergo an additional PET\u002FCT imaging study.",[36],"C-11 ER176 PET\u002FCT",{"type":38,"name":39,"description":40,"armGroupLabels":41},"DIAGNOSTIC_TEST","Blood Test","Participants will undergo a one time venipuncture blood collection to evaluate the presence of inflammatory and genetic markers.",[36],[43,47,50],{"measure":44,"description":45,"timeFrame":46},"Determine if neuroinflammation, as measured by C-11 ER176 SUVr and inflammatory blood test measurements, is correlated with an increase in AB plaque, as measured by C-11 PiB SUVr.","Rationale: Biomarkers that are surrogates of AD pathology are needed to provide methods to select appropriate treatment strategies. We hypothesize that increased neuroinflammation PET signal is seen in AD A+ and MCI A+ as compared to CU A+ participants and is also increased in CU A+ vs. CU A- participants. We note that similar patterns may also be observed in other neurodegenerative diseases such as DLB, particularly in cases with mixed AD pathology.","4 years",{"measure":48,"description":49,"timeFrame":46},"Determine if neuroinflammation, as measured by C-11 ER176 SUVr, is correlated with a history of increased cognitive decline in the 5 years preceding PET imaging, as measured by z scores from neuropsychiatric test results (memory, etc.).","Rationale: Surrogate biomarkers of AD pathology, beyond amyloid and tau, are needed to better assess disease progression and prognosis in AD dementia patients, as well as in DLB patients. We hypothesize that increased ER176 PET signal in amyloid positive participants is associated with the rate of cognitive decline preceding the neuroinflammation PET scan.",{"measure":51,"description":52,"timeFrame":46},"Determine if neuroinflammation, as measured by PET imaging, is associated with blood and\u002For CSF biomarkers of inflammation or other neurologic diseases and related blood tests.","Rationale: Plasma biomarkers are advantageous over imaging and CSF biomarkers with regards to cost, invasiveness, and feasibility in community settings. However, they may be less specific. We need to determine how blood and\u002For CSF biomarkers correlate with PET neuroinflammation imaging as markers of disease progression, which markers are most highly correlated, and which may be specific to AD pathology. We hypothesize that plasma biomarkers of inflammation and other neurologic diseases and related blood tests (cytokines, TSPO, amyloid and tau) will correlate with increased PET neuroinflammation imaging signal.",[54],{"measure":55,"description":56,"timeFrame":57},"Incidence of adverse events attributable to ER176.","Adverse events related to ER176 will be evaluated according to the Common Terminology Criteria for Adverse Events (CTCAE 5.0)","4 year","ALL","60 Years",null,{"inclusion":62,"exclusion":68,"raw_text":73},[63,64,65,66,67],"Males or females 60 years of age or older.","Meet the requirements for one of the five groups (CU A-, CU A+, MCI A+, AD A+, MCI-LB or DLB).","Neurologic evaluation procedures with testing in the MCSA, ADRC, Longitudinal Imaging Biomarkers of Prodromal and Overt DLB studies or Mayo Clinic Behavioral Neurology Practice. Must have had or plan to have at least 2 testing sessions.","All participants must have or plan to have an amyloid PiB PET scan and MRI brain scan within approximately 6 months of the first ER176 PET\u002FCT scan. Participants undergoing an optional additional ER176 scan are preferred, but not required, to have or plan to have an amyloid PiB PET scan and MRI brain scan within approximately 6 months of the second ER176 PET\u002FCT scan.","Capacity to sign consent or have a legally authorized representative to sign the consent.",[69,70,71,72],"Participants unable to lie down without moving for 20 minutes.","Women who are pregnant or cannot stop breast feeding for 24 hours.","Actively taking daily anti-inflammatory medications (NSAIDs, corticosteroids, etc.) except for a small control group.","Generalized inflammatory condition and treatment with immunosuppressive, corticoid\u002Fglucocorticoid, steroidal or non-steroidal anti-inflammatory medication within 2 weeks of scanning (only acute medication use as an exclusion so as to limit medication interaction but preserve possible chronic systemic inflammation interaction).","Inclusion Criteria:\n\n* Males or females 60 years of age or older.\n* Meet the requirements for one of the five groups (CU A-, CU A+, MCI A+, AD A+, MCI-LB or DLB).\n* Neurologic evaluation procedures with testing in the MCSA, ADRC, Longitudinal Imaging Biomarkers of Prodromal and Overt DLB studies or Mayo Clinic Behavioral Neurology Practice. Must have had or plan to have at least 2 testing sessions.\n* All participants must have or plan to have an amyloid PiB PET scan and MRI brain scan within approximately 6 months of the first ER176 PET\u002FCT scan. Participants undergoing an optional additional ER176 scan are preferred, but not required, to have or plan to have an amyloid PiB PET scan and MRI brain scan within approximately 6 months of the second ER176 PET\u002FCT scan.\n* Capacity to sign consent or have a legally authorized representative to sign the consent.\n\nExclusion Criteria:\n\n* Participants unable to lie down without moving for 20 minutes.\n* Women who are pregnant or cannot stop breast feeding for 24 hours.\n* Actively taking daily anti-inflammatory medications (NSAIDs, corticosteroids, etc.) except for a small control group.\n* Generalized inflammatory condition and treatment with immunosuppressive, corticoid\u002Fglucocorticoid, steroidal or non-steroidal anti-inflammatory medication within 2 weeks of scanning (only acute medication use as an exclusion so as to limit medication interaction but preserve possible chronic systemic inflammation interaction).\n* Standard safety exclusionary criteria for MRI such as metallic foreign bodies, pacemaker, etc., since the quantitative PET data analysis is based on anatomic criteria that are established uniquely for each subject by registration to his\u002Fher MRI.",[75,76],"ADULT","OLDER_ADULT",[78],{"facility":79,"city":80,"state":81,"zip":82,"country":83,"geoPoint":84},"Mayo Clinic in Rochester","Rochester","Minnesota","55905","United States",{"lat":85,"lon":86},44.02163,-92.4699,[],[89],{"name":90,"affiliation":91,"role":92},"Val Lowe, MD","Mayo Clinic","PRINCIPAL_INVESTIGATOR",[],[95],{"label":96,"url":97},"Mayo Clinic Clinical Trials","https:\u002F\u002Fwww.mayo.edu\u002Fresearch\u002Fclinical-trials",{"nct_id":4,"conditions":99,"biomarkers":103},[100,101,102],"Alzheimer's Disease","Lewy Body Dementia","Mild cognitive disorder",[],{"nct_id":4,"found":14,"summary":105,"prompt_version":115},{"design":106,"status":107,"heading":108,"summary":109,"follow_up":110,"word_count":111,"commitments":112,"compensation":113,"drugs_mentioned":114},"This interventional study plans to enroll 125 participants. It is not specified if it is randomized, blinded, or what phase it is in.","completed","Investigating Brain Inflammation in Alzheimer's and Related Dementias","This study is looking into how brain inflammation might be connected to Alzheimer's disease (AD) and other dementias like Lewy Body Dementia (LBD). Researchers will use a special imaging scan called PET\u002FCT with a substance called C-11 ER-176 to measure inflammation in the brain. They will also take a blood sample to look for markers of inflammation and genetic factors. The goal is to see if brain inflammation is linked to amyloid-beta (AB) plaques (a hallmark of AD), cognitive decline, or other inflammation markers in the blood. You may be able to join if you are 60 or older and meet specific criteria related to your cognitive status and previous neurological evaluations.","The study will track correlations between neuroinflammation and other factors for up to 4 years.",112,"Participants will receive a one-time administration of C-11 ER-176 and undergo a PET\u002FCT scan. You may be invited for an additional administration and scan. You will also have a one-time blood draw.","Not stated in the trial record.",[33],"v2"]