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Phase 3 N=1,169 Randomized Quadruple-blind Treatment

Clinical Trial of Solanezumab for Older Individuals Who May be at Risk for Memory Loss

Cognition Disorders

Enrolled (actual)
1,169
Serious AEs
23.0%
Results posted
Dec 2023
Primary outcome: Primary: Change From Baseline of the Preclinical Alzheimer Cognitive Composite (PACC) Score — -1.43; -1.13 score on a scale — p=0.260

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
Placebo (Drug); Solanezumab (Drug)
Age
Older Adult · 65+ yrs
Sex
All
Sponsor
Eli Lilly and Company
Primary completion
Dec 2022

Outcome Measures

OutcomeResultp-value
PRIMARY
Change From Baseline of the Preclinical Alzheimer Cognitive Composite (PACC) Score
PRIMARY
Change From Baseline of the Preclinical Alzheimer Cognitive Composite (PACC) Score
SECONDARY
Change From Baseline in Cognitive Function Index (CFI)
SECONDARY
Change From Baseline in Cognitive Function Index (CFI)
SECONDARY
Change From Baseline in Alzheimer's Disease Cooperative Study-Activities Daily Living-Prevention Questionnaire (ADCS-ADL-Prevention Questionnaire) Score
SECONDARY
Change From Baseline in Alzheimer's Disease Cooperative Study-Activities Daily Living-Prevention Questionnaire (ADCS-ADL-Prevention Questionnaire) Score
SECONDARY
Change From Baseline in Mean Composite Standardized Uptake Value Ratio (SUVr)
0.066; 0.108 <0.001 sig
SECONDARY
Change From Baseline in Cerebrospinal Fluid (CSF) Tau Biomarkers
-17.201; -20.440; 10.266; 11.231 0.922
SECONDARY
Change From Baseline of Cerebrospinal Fluid (CSF) Concentrations of Amyloid Beta (Aβ)
12151.386; -587.063; 1045.570; 49.160 <0.001 sig
SECONDARY
Change From Baseline in Brain Volume as Measured by Volumetric Magnetic Resonance Imaging (vMRI)
-0.369; -0.314; 9.329; 8.978 0.161
SECONDARY
Change From Baseline on the Clinical Dementia Rating-Sum of Boxes Score (CDR-SB)
SECONDARY
Change From Baseline on the Computerized Cognitive Composite (C3)

Summary

The purpose of this study is to test whether an investigational drug called solanezumab can slow the progression of memory problems associated with brain amyloid (protein that forms plaques in the brains of people with Alzheimer Disease [AD]).

Eligibility Criteria

Inclusion Criteria

  • Has a Mini-Mental State Examination (MMSE) score at screening of 25 to 30
  • Has a global Clinical Dementia Rating (CDR) scale score at screening of 0
  • Has a Logical Memory II score at screening of 6 to 18
  • Has a florbetapir positron emission tomography (PET) scan that shows evidence of brain amyloid pathology at screening
  • Has a study partner that is willing to participate as a source of information and has at least weekly contact with the participant (contact can be in-person, via telephone or electronic communication)

Exclusion Criteria

  • Is receiving a prescription acetylcholinesterase inhibitor (AChEI) and/or memantine at screening or baseline
  • Lacks good venous access, such that intravenous drug delivery or multiple blood draws would be precluded
  • Has current serious or unstable illness including cardiovascular, hepatic, renal, gastroenterologic, respiratory, endocrinologic, neurologic, psychiatric, immunologic, or hematologic disease or other conditions that, in the investigator's opinion, could interfere with the analyses of safety and efficacy in this study
  • Has had a history within the last 5 years of a serious infectious disease affecting the brain (including neurosyphilis, meningitis, or encephalitis) or head trauma resulting in protracted loss of consciousness
  • Has had a history within the last 5 years of a primary or recurrent malignant disease with the exception of any in situ cancer that was appropriately treated and is being appropriately monitored, such as resected cutaneous squamous cell carcinoma in situ or in situ prostate cancer with normal prostate-specific antigen post-treatment
  • Has a known history of human immunodeficiency virus (HIV), clinically significant multiple or severe drug allergies, or severe post-treatment hypersensitivity reactions (including, but not limited to, erythema multiforme major, linear immunoglobulin A dermatosis, toxic epidermal necrolysis, or exfoliative dermatitis)
  • Is clinically judged by the investigator to be at serious risk for suicide
  • Has a history within the past 2 years of major depression or bipolar disorder as defined by the most current version of the Diagnostic and Statistical Manual of Mental Disorders (DSM)
  • Has a history within the past 5 years of chronic alcohol or drug abuse/dependence as defined by the most current version of the DSM

Open-Label Inclusion Criteria:

  • All participants who complete the placebo-controlled period will be allowed to continue into the open-label period
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02008357). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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