TrialSignal
Clinical trial intelligence report
A Double-Blind, Randomized, Placebo-Controlled, Dose Escalating Study to Evaluate the Safety, Tolerability, and Immunogenicity of V950 Formulated on Aluminum-Containing Adjuvant With or Without ISCOMATRIX™ in Patients With Alzheimer Disease
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT00464334-Jul 28, 2026
NCT ID
NCT00464334
Status
COMPLETED
Phase
PHASE1
Sponsor
Merck Sharp & Dohme LLC
Executive brief
Investment-Ready Snapshot
A Double-Blind, Randomized, Placebo-Controlled, Dose Escalating Study to Evaluate the Safety, Tolerability, and Immunogenicity of V950 Formulated on Aluminum-Containing Adjuvant With or Without ISCOMATRIX™ in Patients With Alzheimer Disease is a PHASE1 clinical asset sponsored by Merck Sharp & Dohme LLC in Alzheimer Disease. SEO and diligence focus: V950, ISCOMATRIX™, Placebo to V950, endpoint relevance, enrollment feasibility, competitive positioning, readout timing and IP durability.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT00464334
Indication
Alzheimer Disease
Modality
protein therapy
Target
V950, ISCOMATRIX™, Placebo to V950
Intervention
V950, ISCOMATRIX™, Placebo to V950
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.