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Clinical trial intelligence report
An Open-Label Extension To The B1451006 Protocol To Evaluate The Safety And Efficacy Of Dimebon (Latrepirdine, PF-01913539) In Subjects With Moderate-To-Severe Alzheimer's Disease
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 18, 2026
NCT ID
NCT01066546
Status
TERMINATED
Phase
Phase 3
Sponsor
Pfizer
Executive brief
Investment-Ready Snapshot
The clinical trial for Dimebon in moderate-to-severe Alzheimer's disease was terminated due to a lack of demonstrated efficacy in prior studies, specifically the DIM14 (CONNECTION) Study. This raises significant concerns regarding the asset's viability in a competitive market where effective treatments for Alzheimer's are in high demand. The termination may impact Pfizer's strategic positioning in the neurodegenerative disease space, as the company may need to pivot resources towards more promising candidates. Additionally, the collaboration with Medivation, Inc. may require reassessment in light of this outcome. The Alzheimer's market remains lucrative, but the failure of Dimebon could hinder Pfizer's market share and investor confidence.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT01066546
Indication
Alzheimer's Disease
Modality
small molecule
Target
Dimebon (Latrepirdine) - Mechanism of action not fully elucidated; previously hypothesized to modulate mitochondrial function and exert neuroprotective effects.
Intervention
Dimebon tablet for oral administration
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.