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NCT06079190

Efficacy and Safety of GSK4527226 [AL101] in Participants With Early Alzheimer's Disease

Last Updated: 2025-11-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

PHASE2

Total Enrollment

367 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-10-20

Study Completion Date

2026-11-23

Brief Summary

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The aim of this study is to assess the efficacy and safety of GSK4527226 in participants with early Alzheimer's Disease (AD) (including mild cognitive impairment \[MCI\] and mild dementia due to AD) of 2 dose levels of GSK4527226 compared to placebo.

Detailed Description

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Conditions

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Alzheimer's Disease

Keywords

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Alzheimer Disease Dementia Brain Diseases Central Nervous System Diseases Nervous System Diseases Mental Disorders

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors

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Study Groups

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GSK4527226 Dose 1

Participants will receive GSK4527226 Dose 1

Group Type EXPERIMENTAL

GSK4527226

Intervention Type DRUG

GSK4527226 will be administered.

GSK4527226 Dose 2

Participants will receive GSK4527226 Dose 2

Group Type EXPERIMENTAL

GSK4527226

Intervention Type DRUG

GSK4527226 will be administered.

Placebo

Participants will receive placebo.

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type OTHER

Placebo will be administered.

Interventions

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GSK4527226

GSK4527226 will be administered.

Intervention Type DRUG

Placebo

Placebo will be administered.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

Participant must be in the Alzheimer's continuum as defined by the 2018 National Institute on Aging and Alzheimer's Association (NIAAA) Research Framework corresponding to the clinical categories of MCI due to AD and mild AD dementia.

Participant must have evidence of amyloid positivity either by positive positron emission tomography (PET) result (Amyloid PET scans must be read by a central imaging lab) or cerebrospinal fluid (CSF) amyloid beta (Aβ) test result indicative of amyloid positivity

* Participants must also meet the following criteria for clinical severity:

1. MMSE score of between 21 and 29 points
2. CDR-global score (GS) of 0.5 to 1.0.
3. CDR Memory Box score greater than or equal to (≥) 0.5.
4. Participants with objective impairment in episodic memory as indicated by at least 1 standard deviation below age-adjusted mean in the Wechsler Memory Scale-IV Logical Memory II (WMS-IV LMII)
* If the participant is receiving symptomatic AD medications such as an Acetylcholinesterase inhibitor (AChEI) or memantine, the dosing regimen must have been stable for at least 12 weeks prior to screening and is not expected to change during study participation.
* If the participant is receiving other medications for AD related symptoms or associated conditions, the dosing regimen must have been stable for at least 4 weeks prior to screening and not expected to change during study participation. Symptoms must be considered adequately and stably controlled by the investigator, without marked changes in medication anticipated for the duration of the study.
* Body weight ≥ 45 kilogram (kg) to less than or equal to (≤)120 kg with body mass index (BMI) between 17 and 34.9 kilogram per meter square (kg/m\^2), inclusive.
* A female participant is eligible to participate if she is not pregnant or breastfeeding, and if of child-bearing potential follows contraception requirements outlined in the protocol
* A male participant is eligible to participate if he follows contraception requirements outlined in the protocol
* Willing and able to give informed consent which includes compliance with the requirements and restrictions listed in the informed consent form (ICF).
* Availability of an adult person who has frequent and sufficient contact with the participant is able to provide accurate information regarding the participant's cognitive and functional abilities, agrees to provide information at clinic visits, and signs the ICF of the study partner.

Exclusion Criteria

Participant has evidence of any neurological condition other than AD that may contribute to cognitive impairment.

* History or presence of vascular disease that has the potential to affect cognitive function.
* History or presence of stroke within the past 1 year or recent transient ischemic attack within 180 days before screening.
* History of severe, clinically significant central nervous system (CNS) trauma.
* History or presence of intracranial tumor.
* Presence of ongoing infection(s) that may affect brain function, or history of infections that resulted in neurologic sequelae.
* History of primary psychiatric diagnosis that the investigator considers may interfere with study assessments.

Columbia Suicide Severity Rating Scale (C-SSRS) suicidal ideation Type 4 or 5, suicidal behaviour or has been assessed to be at risk of suicide, in the opinion of the investigator within 6 months before screening, at screening, or at the Baseline visit, or has been hospitalized or treated for suicidal behaviour in the past 2 years.

* Participant has history of alcohol and/or moderate to severe substance use disorder within the past 2 years
* Magnetic resonance imaging (MRI) evidence based on central read of:

1. \>3 lacunar infarcts.
2. Stroke involving a major vascular territory, severe small vessel, or white matter disease.
3. Any territorial /cortical/other infarct \>1 cubic centimetre (cm\^3).
4. White matter hyperintense lesions on the FLAIR sequence that correspond to an overall Fazekas score of 3
5. \>4 microhaemorrhages.
6. Any areas of superficial (leptomeningeal) hemosiderosis.
7. A single macro-hemorrhage greater than 10 millimetres (mm) at greatest diameter.
8. Vasogenic edema.
9. Cerebral contusion, encephalomalacia, aneurysms, vascular malformations, or infective lesions.
10. Space occupying lesions or brain tumors.
11. Significant cerebral vascular pathology
12. Hydrocephalus/Normal pressure hydrocephalus.
13. Other MRI findings contraindicating participation in the study such as subarachnoid hemorrhage.
* History suggestive of exposure to, or past tuberculosis (TB) infection should undergo screening for TB disease.
* Chronic active immune disorder requiring systemic immunosuppressive therapy within 6 months prior to Screening.
* Screening serum vitamin B12 concentration \< Lower limit of normal (LLN) or in the low normal range
* Folate \<LLN or Thyroid-stimulating hormone (TSH) \> Upper limit of normal (ULN)
* Hemoglobin A1c \>8 percentage (%) or poorly controlled diabetes during the last 12 weeks
* History of cancer
* Known history of severe allergic, anaphylactic, or other hypersensitivity reactions to chimeric, human, or humanized antibodies or fusion proteins
* Planned surgery during the study which requires general, spinal, or epidural anesthesia that would take place during the study.
* Known genetic predisposition for clotting disorder or hemorrhagic disease.
* Key exclusionary medications include:

* Antipsychotics, opiates/opioids, cannabinoids, hypnotics, antidepressants, mood stabilizers, or stimulants that are used on a chronic basis, are exclusionary if not consistent with the following rule: treatment has to have been at a stable dose for at least 4 weeks before screening and should remain stable during the study
* Any biologic drugs with systemic exposure, whether investigational or approved, used within 6 months before screening Any disease modification drug for AD, such as aducanumab and lecanemab, whether investigational or approved, used within 6 months before screening.
* Anticoagulation medications within 90 days of screening and during the study
* Systemic immunosuppressive therapy within 6 months before screening and during the study.

Minimum Eligible Age

50 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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GSK Clinical Trials

Role: STUDY_DIRECTOR

GlaxoSmithKline

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2023-505083-11-00

Identifier Type: REGISTRY

Identifier Source: secondary_id

219867

Identifier Type: -

Identifier Source: org_study_id

Efficacy and Safety of GSK4527226 [AL101] in Participants With Early Alzheimer's Disease

Study Results

Basic Information

Brief Summary

Detailed Description

Conditions

Keywords

Study Design

Study Groups

GSK4527226 Dose 1

GSK4527226

GSK4527226 Dose 2

GSK4527226

Placebo

Placebo

Interventions

GSK4527226

Placebo

Eligibility Criteria

Inclusion Criteria

Exclusion Criteria

Sponsors

Alector Inc.

GlaxoSmithKline

Responsible Party

Principal Investigators

GSK Clinical Trials

Locations

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