TrialSignal
Clinical trial intelligence report
Evaluation of [123I] MNI-308 and SPECT as a Marker of Beta-amyloid Protein Deposition in Subjects With Alzheimer Disease in Comparison to Healthy Subjects
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT00544453-Jul 28, 2026
NCT ID
NCT00544453
Status
TERMINATED
Phase
Phase 1
Sponsor
Molecular NeuroImaging
Executive brief
Investment-Ready Snapshot
The clinical trial for [123I] MNI-308, sponsored by Molecular NeuroImaging, aimed to evaluate its efficacy as an imaging biomarker for beta-amyloid burden in Alzheimer's disease (AD) patients compared to healthy controls. The termination of the trial due to preliminary data indicating that [123I] MNI-308 is not a useful tool for detecting AD suggests significant challenges in the market for imaging agents targeting amyloid deposition. This outcome may limit the commercial viability of [123I] MNI-308 and reflects broader competitive pressures in the neuroimaging market, particularly as other imaging modalities and biomarkers are being explored. Stakeholders should consider the implications of this termination for future investment and development strategies in neurodegenerative disease diagnostics.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT00544453
Indication
Alzheimer Disease
Modality
small molecule
Target
Beta-amyloid protein deposition in the brain
Intervention
[123I] MNI-308
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.