TrialSignal
Clinical trial intelligence report
Single-Ascending Dose, Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Study of LY2886721 in Healthy Subjects
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT01133405-Jul 28, 2026
NCT ID
NCT01133405
Status
COMPLETED
Phase
Phase 1
Sponsor
Eli Lilly and Company
Executive brief
Investment-Ready Snapshot
LY2886721, developed by Eli Lilly and Company, is positioned within the competitive landscape of Alzheimer's Disease therapeutics, targeting a critical mechanism associated with amyloid beta production. The completion of this Phase 1 study indicates progress towards understanding the safety and pharmacokinetics of LY2886721, which may enhance Eli Lilly's portfolio in a market characterized by high unmet needs and significant competition from other amyloid-targeting therapies. The results could inform future development strategies and potential partnerships, as well as influence investor sentiment regarding Eli Lilly's pipeline in neurodegenerative diseases.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT01133405
Indication
Alzheimer's Disease
Modality
small molecule
Target
LY2886721 targets the inhibition of gamma-secretase, an enzyme involved in the cleavage of amyloid precursor protein (APP), which is implicated in the pathogenesis of Alzheimer's Disease.
Intervention
LY2886721, Placebo
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.