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A First-In-Human Study of LY3954068 in Participants With Early Symptomatic Alzheimer's Disease

Recruiting · Phase 1 · NCT06297590

Conditions: Alzheimer Disease

At a glance

Research payments reported, 2025
$3.5M
U.S. investigators named
7
Sites paid
9
Planned or actual enrollment
56

About the trial

Sponsor
Eli Lilly and Company
Tested
LY3954068 (drug), Placebo (drug), Flortaucipir F18 (drug)
Dates
Started 2024-08-15; completion 2028-07
Results posted
Not yet

The main purpose of this study is to evaluate the safety of LY3954068 in participants with early symptomatic Alzheimer's Disease (AD). The study will also investigate how much LY3954068 gets into the bloodstream and will test the effects of LY3954068 on markers of AD. The study will be comprised of two parts, A and B. Each enrolled participant in Part A will receive a single dose of LY3954068 or placebo (no active drug) given into the spinal fluid. Each participant in Part B will receive up to 4 doses of either LY3954068 or placebo administered into the spinal fluid. Participants may have the opportunity to join an optional bridging period to a separate potential study where participants …

From ClinicalTrials.gov, last updated 2026-10-29. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Eli Lilly and Company reported $3.5M in research payments for this study in 2025 (17 payments).

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.