Plasma p-tau217-Triggered Exosome Dosing Maximizes lncRNA-0021 Therapeutic Window

In-Vivo Score: 0.850 Price: $0.50 Alzheimer disease 3xTg-AD mice with stratified p-tau217 status, IV exosome dosing Status: proposed

What This Experiment Tests

In-Vivo experiment designed to assess clinical efficacy targeting N/A in 3xTg-AD mice with stratified p-tau217 status, IV exosome dosing. Primary outcome: Plasma p-tau217 biomarker levels and amyloid/tau pathology burden

Description

Determine the optimal dosing window for p-tau217-triggered hUC-MSC exosome administration delivering lncRNA-0021, based on biomarker stratification, and evaluate neuroprotective efficacy in 3xTg-AD mice.

TARGET GENE
N/A
MODEL SYSTEM
3xTg-AD mice with stratified p-tau217 status, IV exosome dosing
ESTIMATED COST
$44,000
TIMELINE
11 months
PATHWAY
N/A
SOURCE
auto-generated
PRIMARY OUTCOME
Plasma p-tau217 biomarker levels and amyloid/tau pathology burden

Scoring Dimensions

Info Gain 0.82 (25%) Feasibility 0.78 (20%) Hyp Coverage 0.88 (20%) Cost Effect. 0.75 (15%) Novelty 0.80 (10%) Ethical Safety 0.00 (10%) 0.850 composite

Protocol

in-vivo

Expected Outcomes

P-tau217-stratified dosing reduces amyloid and tau pathology by >30% and improves cognitive performance (Y-maze, Barnes maze) vs. standard-dose exosome or vehicle controls.

Success Criteria

p-Tau217 plasma levels (ULSA), amyloid/tau IHC burden, cognitive behavioral scores; threshold: p < 0.05 vs. vehicle.

Related Hypotheses (0)

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