Efficacy and Safety of GSK4527226 [AL101] in Participants With Early Alzheimer's Disease
- Disease/Condition
- Alzheimer's Disease
- Drug/Device/Intervention
- GSK4527226
- Study type
- Interventional
- Intervention type
- drug
- Primary sponsor
- GlaxoSmithKline
- Location
- San Diego,DeLand,Maitland,Miami,Orlando,Stuart,The Villages,Wellington,Decatur,Elk Grove Village,Wichita,Chesterfield,Toms River,New York,New York,Staten Island,Matthews,North Canton,Oklahoma City,Por, Argentina,Australia,Canada,Finland,France,Germany,Italy,Netherlands,Norway,South Korea,Spain,Sweden,
- Phase
- Phase 2
- Start date
- Oct 11, 2023
- End date
- May 16, 2029
- Enrollment
- 282 participants
Change from Baseline in Clinical Dementia Rating - Sum of Boxes (CDR-SB) Score for Dose 1 vs Placebo Across Weeks 52, 64 and 76
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.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT06079190
- Type
- Non-Device Trial
Access comprehensive clinical trial information for NCT06079190 through Pure Global AI's free database. This Phase 2 trial is sponsored by GlaxoSmithKline and is currently Not yet recruiting. The study focuses on Alzheimer's Disease. Target enrollment is 282 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.