TrialSignal
Clinical trial intelligence report
A Study of the Effect of Concomitant Administration of BMS-708163 on the Pharmacokinetics of Donepezil in Healthy Subjects
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT01042314-Jul 28, 2026
NCT ID
NCT01042314
Status
COMPLETED
Phase
PHASE1
Sponsor
Bristol-Myers Squibb
Executive brief
Investment-Ready Snapshot
A Study of the Effect of Concomitant Administration of BMS-708163 on the Pharmacokinetics of Donepezil in Healthy Subjects is a PHASE1 clinical asset sponsored by Bristol-Myers Squibb in Alzheimer Disease. SEO and diligence focus: Donepezil, BMS-708163, endpoint relevance, enrollment feasibility, competitive positioning, readout timing and IP durability.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT01042314
Indication
Alzheimer Disease
Modality
small molecule
Target
Donepezil, BMS-708163
Intervention
Donepezil, BMS-708163
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.