A Study of E2814 With Concurrent Lecanemab Treatment in Participants With Early Alzheimer's Disease

A Phase 2, Placebo-Controlled, Double-Blind, Parallel-Group, Dose-Finding Study to Evaluate Safety, Tolerability, and Biomarker Efficacy of E2814 With Concurrent Lecanemab Treatment in Subjects With Early Alzheimer's Disease

The primary objective of the study is to determine the dose response of E2814, when concurrently administered with lecanemab, on the change from baseline at 6 months in cerebrospinal fluid (CSF) microtubule-binding region (MTBR)-tau-243 in participants with early Alzheimer's disease (AD).

Study Overview

• Status: Active, not recruiting
• Conditions: Alzheimer's Disease
• Intervention / Treatment: Drug: Lecanemab; Drug: E2814; Drug: Placebo

• Study Type: Interventional
• Enrollment (Actual): 105
• Phase: Phase 2

Contacts and Locations

Study Locations

• Japan
  • Osaka, Japan, 545-8586
    • Osaka Metropolitan University Hospital
  • Yamagata, Japan, 990-0834
    • Yamagata Tokushukai Hospital
  • Aichi-ken
    • Ōbu, Aichi-ken, Japan, 474-8511
      • National Center for Geriatrics and Gerontology
  • Hiroshima
    • Ōtake, Hiroshima, Japan, 739-0696
      • National Hospital Organization Hiroshima-Nishi Medical Center
  • Miyazaki
    • Honjō, Miyazaki, Japan, 880-1111
      • Keimei Memorial Hospital
  • Okayama-ken
    • Kurashiki, Okayama-ken, Japan, 710-0813
      • Rijikai Medical Corporation Katayama Medical Clinic
  • Tokyo
    • Shinjuku, Tokyo, Japan, 160-8582
      • Keio University Hospital
    • Shinjuku, Tokyo, Japan, 160-0023
      • Tokyo Medical University Hospital
• United States
  • Arizona
    • Phoenix, Arizona, United States, 85006
      • Banner Sun Health Research
  • Connecticut
    • New Haven, Connecticut, United States, 06510
      • Yale University School of Medicine
  • Florida
    • Bradenton, Florida, United States, 34205
      • Bradenton Research Center
    • Clermont, Florida, United States, 34711
      • K2 Medical Research
    • Miami, Florida, United States, 33165
      • Advanced Clinical Research Network
    • Ocala, Florida, United States, 34470
      • Renstar Medical Research
    • Port Orange, Florida, United States, 32124
      • Progressive Medical Research
    • Stuart, Florida, United States, 34997
      • Alzheimer's Research and Treatment Center-Stuart
    • Tampa, Florida, United States, 33609
      • Axiom Brain Health
    • The Villages, Florida, United States, 32162
      • Charter Research
    • Wellington, Florida, United States, 33467
      • Alzheimer's Research and Treatment Center
  • Georgia
    • Columbus, Georgia, United States, 31909
      • Columbus Memory Center, PC
  • Mississippi
    • Hattiesburg, Mississippi, United States, 39401
      • Hattiesburg Clinic
  • Missouri
    • St Louis, Missouri, United States, 63110
      • Washington University School of Medicine
  • Pennsylvania
    • Abington, Pennsylvania, United States, 19001
      • Abington Neurological Associates Ltd
  • Tennessee
    • Cordova, Tennessee, United States, 38018
      • Neurology Clinic, P.C.
  • Texas
    • Dallas, Texas, United States, 75231
      • Kerwin Memory Center
  • Virginia
    • Richmond, Virginia, United States, 23294
      • National Clinical Research-Richmond, Inc

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

1. For participants diagnosed with mild cognitive impairment (MCI) due to AD-intermediate likelihood:

   1. Meet the National Institute on Aging-Alzheimer's Association (NIA-AA) core clinical criteria for MCI due to AD-intermediate likelihood
   2. Have a global Clinical Dementia Rating Scale (CDR) score of 0.5 and a CDR Memory Box score of greater than or equal to (>=) 0.5 at Screening

2. For participants diagnosed with mild AD dementia:

   1. Meet the NIA-AA core clinical criteria for probable AD dementia
   2. Have a global CDR score of 0.5 to 1.0 and a CDR Memory Box score of >=0.5 at Screening
3. Mini Mental State Examination (MMSE) score >=22 at Screening and less than or equal to (<=) 30 at Screening
4. Able to have CSF lumbar puncture performed and not on, or have a medical condition that may require initiation of, any anticoagulant therapy at Screening
5. Male or female participants aged between >=50 years and <=80 years, at the time of informed consent
6. If receiving an approved AD symptomatic treatment (such as acetylcholinesterase inhibitors (AchEIs), memantine, or both) for AD, participants must be on a stable dose for at least 12 weeks before Baseline. Treatment-naïve participants for AD medications can be enrolled into the study. Unless otherwise stated, participants must have been on stable doses of all other (that is, non AD-related) permitted concomitant medications for at least 4 weeks before Baseline. Use of memantine will not be allowed at screening for participants in Japan
7. Have an identified study partner (defined as a person able to support the participant for the duration of the study and who spends at least 8 hours per week with the participant).
8. Provide written informed consent. If a participant lacks the capacity to consent in the Investigator's opinion, the participants' assent should be obtained, if required in accordance with local laws, regulations, and customs, plus the written informed consent of a legal representative should be obtained (capacity to consent and definition of legal representative should be determined in accordance with applicable local laws and regulations)
9. Willing and able to comply with all aspects of the protocol including multiple CSF collections

Exclusion Criteria:

1. Any neurological condition that may be contributing to cognitive impairment above and beyond that caused by the participant's AD
2. History of transient ischemic attacks, stroke, or seizures within 12 months of Screening
3. Any psychiatric diagnosis or symptoms (example, hallucinations, major depression, or delusions) that could interfere with study procedures in the participants. Psychotic disorder(s) or unstable recurrent affective disorder(s) evident by use of antipsychotics within 2 years before Screening
4. Contraindications to MRI scanning, including cardiac pacemaker/defibrillator, ferromagnetic metal implants (example, in skull and cardiac devices other than those approved as safe for use in MRI scanners). Evidence of other clinically significant lesions on brain MRI at Screening that could indicate a dementia diagnosis other than AD. Other significant pathological findings on brain MRI at Screening, including but not limited to: greater than 4 microhemorrhages (defined as 10 millimeter (mm) or less at the greatest diameter); a single intracerebral hemorrhage greater than 10 mm at greatest diameter; an area of superficial siderosis; evidence of vasogenic edema; evidence of cerebral contusion, encephalomalacia, aneurysms, vascular malformations, or infective lesions; evidence of multiple lacunar infarcts or stroke involving a major vascular territory, severe small vessel, or white matter disease; space occupying lesions; or brain tumors (however, lesions diagnosed as meningiomas or arachnoid cysts and less than 1 cm at their greatest diameter need not be exclusionary). Other minor or clinically insignificant magnetic resonance imaging (MRI) abnormalities, as agreed by the medical monitor and after discussion with the investigator, may not be exclusionary
5. Malignant neoplasms within 3 years of Screening (except for basal or squamous cell carcinoma in situ of the skin, or localized prostate cancer in male participants, or localized breast cancer in female participants). Participants who had malignant neoplasms but who have had at least 3 years of documented uninterrupted remission before Screening need not be excluded
6. A clinically significant ECG abnormality, including a marked prolonged corrected QT interval (Fridericia's Correction Formula; QTcF) interval (example, a repeated demonstration of a QTcF interval greater than (>) 450 milliseconds [ms])
7. Participants with a bleeding disorder that is not under adequate control (including a platelet count <50,000 or international normalized ratio [INR] >1.5). Any participants who are on anticoagulant therapy are not permitted to be enrolled
8. Have thyroid-stimulating hormone above normal range. Other tests of thyroid function with results outside the normal range should only be exclusionary if they are considered clinically significant by the investigator. This applies to all participants whether or not they are taking thyroid supplements
9. Abnormally low serum vitamin B12 levels for the testing laboratory (if participant is taking vitamin B12 injections, level should be at or above the lower limit of normal for the testing laboratory). Levels of vitamin B12 may be confirmed with reflex testing to include methylmalonic acid analysis, if available in region
10. Any suicidal ideation with intent with or without a plan at Screening, Baseline, or within 6 months of Screening (that is, answering "Yes" to questions 4 or 5 on the Suicidal Ideation section of the Columbia-Suicide Severity Rating Scale [C-SSRS]) Type 4 or 5, or any suicidal behavior assessment within 6 months before Screening, at Screening, or at the Baseline Visit, or has been hospitalized or treated for suicidal behavior in the past 5 years before Screening)
11. Evidence of clinically significant disease (example, cardiac, respiratory, gastrointestinal, and renal disease) that in the opinion of the investigator(s) could affect the participants safety or interfere with the study assessments. Any other medical conditions (example, cardiac, respiratory, gastrointestinal, and renal disease) that are not stably and adequately controlled or that in the opinion of the investigator(s) could affect the participant's safety or interfere with the study assessments
12. Hypersensitivity to lecanemab, E2814, or any of the excipients
13. Any immunological disease, that is not adequately controlled, or that requires treatment with immunoglobulins, systemic monoclonal antibodies (mAbs) (or derivatives of mAbs), systemic immunosuppressants, or plasmapheresis during the study
14. Any history of or concomitant medical condition that in the opinion of the investigator(s) would compromise the participant's ability to safely complete the study
15. Planned surgery that requires general, spinal, or epidural anesthesia that would take place during the study. Planned surgery that requires only local anesthesia and that can be undertaken as a day case without inpatient stay postoperatively need not result in exclusion if in the opinion of the investigator this operation does not interfere with study procedures and participant safety
16. Known to be human immunodeficiency virus positive
17. Known or suspected history of drug or alcohol abuse or dependence within 2 years before Screening or a positive urine drug test at Screening. Participants who test positive for benzodiazepines or opioids in urine drug testing need not be excluded if in the clinical opinion of the investigator, this is due to the participant taking prior/concomitant medications containing benzodiazepines or opioids for a medical condition and not due to drug abuse
18. Severe visual or hearing impairment that would prevent the participant from performing psychometric tests accurately
19. Participation in a clinical study involving any antiamyloid plaque lowering or anti-tau therapies (including any mAb and antisense oligonucleotide therapies unless it can be documented that the subject only received placebo)
20. Participation in a clinical study involving any therapeutic mAb, protein derived from a mAb, immunoglobulin therapy, or vaccine within 6 months before Screening unless it can be documented that the subject only received placebo

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Quadruple

Number of Arms

5

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: E2814 Dose A + Lecanemab; Participants will receive E2814 Dose A administered as an intravenous (IV) infusion, every four weeks (Q4W) along with lecanemab administered as a subcutaneous (SC) injection, every week (QW).	Drug: Lecanemab; Lecanemab SC injection.; Other Names: BAN2401; LEQEMBI; Drug: E2814; E2814 IV infusion.
Experimental: E2814 Dose B + Lecanemab; Participants will receive E2814 Dose B administered as an IV infusion, Q4W along with lecanemab administered as a SC injection, QW.	Drug: Lecanemab; Lecanemab SC injection.; Other Names: BAN2401; LEQEMBI; Drug: E2814; E2814 IV infusion.
Experimental: E2814 Dose C + Lecanemab; Participants will receive E2814 Dose C administered as an IV infusion, Q4W along with lecanemab administered as a SC injection, QW.	Drug: Lecanemab; Lecanemab SC injection.; Other Names: BAN2401; LEQEMBI; Drug: E2814; E2814 IV infusion.
Experimental: E2814 Dose D + Lecanemab; Participants will receive E2814 Dose D administered as an IV infusion, Q4W along with lecanemab administered as a SC injection, QW.	Drug: Lecanemab; Lecanemab SC injection.; Other Names: BAN2401; LEQEMBI; Drug: E2814; E2814 IV infusion.
Experimental: Placebo + Lecanemab; Participants will receive placebo administered as an IV infusion, Q4W along with lecanemab administered as a SC injection, QW.	Drug: Lecanemab; Lecanemab SC injection.; Other Names: BAN2401; LEQEMBI; Drug: Placebo; Placebo IV infusion.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Change From Baseline in CSF MTBR-tau-243 at 6 Months	Baseline at 6 months

Secondary Outcome Measures

Outcome Measure	Time Frame
Change From Baseline in Tau Positron Emission Tomography (PET) up to 24 Months	Baseline up to 24 months
Change From Baseline in Clinical Dementia Rating Scale-Sum of Boxes (CDR-SB) up to 24 Months	Baseline up to 24 months
Change From Baseline in Alzheimers Disease Cooperative Scale-Activities of Daily Living Mild Cognitive Impairment Version (ADCS MCI-ADL) up to 24 Months	Baseline up to 24 months
Serum Anti-E2814 Antibody (ADA) Concentration	Baseline up to 27 months
AUC: Area Under the Serum Concentration Versus Time Curve of E2814	Baseline up to 27 months
Cav: Average Serum Concentration of E2814	Baseline up to 27 months
Number of Participants With Treatment-emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs)	From first dose of the study drug up to 27 months
Number of Participants With Markedly Abnormal Laboratory Parameters	From first dose of the study drug up to 27 months
Number of Participants With Clinically Significant Vital Signs Values	From first dose of the study drug up to 27 months
Number of Participants With Clinically Significant Electrocardiogram (ECG) Findings	From first dose of the study drug up to 27 months

Collaborators and Investigators

• Sponsor: Eisai Inc.

Study record dates

Study Major Dates

• Study Start (Actual): September 30, 2024
• Primary Completion (Estimated): December 3, 2026
• Study Completion (Estimated): August 18, 2027

Study Registration Dates

• First Submitted: September 16, 2024
• First Submitted That Met QC Criteria: September 16, 2024
• First Posted (Actual): September 19, 2024

Study Record Updates

• Last Update Posted (Actual): February 11, 2026
• Last Update Submitted That Met QC Criteria: February 9, 2026
• Last Verified: January 1, 2026

More Information

Terms related to this study

• Keywords: Lecanemab; E2814; Early Alzheimer's Disease
• Additional Relevant MeSH Terms: Brain Diseases; Central Nervous System Diseases; Nervous System Diseases; Mental Disorders; Neurocognitive Disorders; Dementia; Tauopathies; Neurodegenerative Diseases; Alzheimer Disease; lecanemab
• Other Study ID Numbers: E2814-G000-202

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: YES
• IPD Plan Description: Eisai's data sharing commitment and further information on how to request data can be found on our website http://eisaiclinicaltrials.com/.

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: Yes
• Studies a U.S. FDA-regulated device product: No