Informed Consent
Item
willing and able to give written informed consent
boolean
C0021430 (UMLS CUI [1])
Mild cognitive disorder | Alzheimer's Disease Mild
Item
meet the diagnostic criteria for either amnestic mild cognitive impairment (amnestic mci) or mild alzheimer's disease (ad).
boolean
C1270972 (UMLS CUI [1])
C0002395 (UMLS CUI [2,1])
C2945599 (UMLS CUI [2,2])
Brain scan structural | Comorbidity Absent | Pathology Vascular Absent | Exception White matter changes Age Related | Exception White matter changes Incidental
Item
structural brain scan within the last 6 months prior to randomization that indicates no other underlying disease, in particular no evidence for vascular pathology except for normal age-related white matter/incidental white matter changes which is normal for this age group.
boolean
C0596217 (UMLS CUI [1,1])
C0678594 (UMLS CUI [1,2])
C0009488 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0677042 (UMLS CUI [3,1])
C1801960 (UMLS CUI [3,2])
C0332197 (UMLS CUI [3,3])
C1705847 (UMLS CUI [4,1])
C1833300 (UMLS CUI [4,2])
C0001779 (UMLS CUI [4,3])
C0439849 (UMLS CUI [4,4])
C1705847 (UMLS CUI [5,1])
C1833300 (UMLS CUI [5,2])
C0444507 (UMLS CUI [5,3])
Contact with Primary caregiver Daily | Contact with Partner Daily
Item
daily contact with a primary caregiver/partner
boolean
C0332158 (UMLS CUI [1,1])
C1319883 (UMLS CUI [1,2])
C0332173 (UMLS CUI [1,3])
C0332158 (UMLS CUI [2,1])
C3887537 (UMLS CUI [2,2])
C0332173 (UMLS CUI [2,3])
Immunotherapy Targeting Amyloid beta
Item
immune therapy targeting alzheimer beta amyloid within the last 12 months
boolean
C0021083 (UMLS CUI [1,1])
C1521840 (UMLS CUI [1,2])
C0078939 (UMLS CUI [1,3])
Institutionalized
Item
institutionalized
boolean
C0562359 (UMLS CUI [1])
Disability Preventing Protocol Compliance | Blind Vision | Deafness | Verbal impairment
Item
disability that may prevent completion of all study requirements (e.g., blindness, deafness, or communication difficulty)
boolean
C0231170 (UMLS CUI [1,1])
C1292733 (UMLS CUI [1,2])
C0525058 (UMLS CUI [1,3])
C0456909 (UMLS CUI [2])
C0011053 (UMLS CUI [3])
C0566027 (UMLS CUI [4])
Tobacco use | Urine cotinine measurement
Item
reported use of tobacco products in the previous 3 months or have a urine cotinine level greater than 500 ng/ml
boolean
C0543414 (UMLS CUI [1])
C1278256 (UMLS CUI [2])
Medical History ECG abnormality | Family history Prolonged QT interval
Item
past medical history of clinically significant electrocardiogram (ecg) abnormalities or a family history (grandparents, parents, and siblings) of prolonged qt-interval syndrome
boolean
C0262926 (UMLS CUI [1,1])
C0522055 (UMLS CUI [1,2])
C0241889 (UMLS CUI [2,1])
C0151878 (UMLS CUI [2,2])
Condition Specified Study Protocol
Item
history or current diagnosis of conditions specified in the protocol.
boolean
C0348080 (UMLS CUI [1,1])
C0205369 (UMLS CUI [1,2])
C2348563 (UMLS CUI [1,3])
Clinical Trial Eligibility Criteria Study Protocol
Item
other protocol-defined inclusion/exclusion criteria may apply.
boolean
C1516637 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])