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Senolytic Therapy (D+Q) Phase IIa Trial in Early Alzheimer's Disease
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experiment
Created: 2026-04-02T10:01:41
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ID: experiment-exp-wiki-experiments-senolyti
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SUMMARY
# Senolytic Therapy (D+Q) Phase IIa Trial in Early Alzheimer's Disease
## Background and Rationale
This Phase IIa clinical trial evaluates the therapeutic potential of senolytic therapy using dasatinib plus quercetin (D+Q) in early Alzheimer's disease patients, targeting the senescence-associated secretory phenotype (SASP) that contributes to neuroinflammation and cognitive decline. Cellular senescence accumulates in the aging brain and is accelerated in AD, with senescent cells secreting pro-in
METHODOLOGY NOTES
**Phase 1: Screening and Baseline Assessment (Weeks -4 to 0)**
• Screen 200 potential participants aged 60-85 with mild cognitive impairment or early AD (CDR 0.5-1.0)
• Confirm amyloid positivity via PET imaging (Centiloid >20) or CSF Aβ42/40 ratio <0.067
• Obtain comprehensive neuropsychological battery (ADAS-Cog, MMSE, CDR-SB, FAQ)
• Collect baseline blood biomarkers: p16INK4a, p21, IL-6, TNF-α, SASP factors
• Perform baseline brain MRI with volumetric analysis and DTI sequences
• Lumbar puncture for CSF collection: Aβ40, Aβ42, tau, p-tau181, neurofilament light
• Randomize 120 eligible participants 1:1 to D+Q vs placebo arms (n=60 each)
**Phase 2: Treatment Period (Weeks 1-24)**
• Administer dasatinib 100mg + quercetin 1000mg orally for 2 consecutive days every 4 weeks (6 cycles total)
• Placebo group receives matched capsules on same schedule
• Safety monitoring every 2 weeks: CBC, comprehensive metabolic panel, liver enzymes
• Cognitive assessments at weeks 4, 8, 12, 18, and 24
•
▸Metadatasource: {'type': 'manual', 'source_name': 'wiki'
| source | {'type': 'manual', 'source_name': 'wiki', 'extracted_by': 'backfill_v1', 'extraction_date': '2026-04-16T01:00:16.907032Z'} |
| summary | # Senolytic Therapy (D+Q) Phase IIa Trial in Early Alzheimer's Disease ## Background and Rationale This Phase IIa clinical trial evaluates the therapeutic potential of senolytic therapy using dasatini |
| entities | {'genes': ['SASP'], 'diseases': ["Alzheimer's Disease"]} |
| model_system | human |
| _schema_version | 1 |
| experiment_type | clinical |
| primary_outcome | Change from baseline in cerebrospinal fluid SASP inflammatory markers (IL-6, TNF-α, IL-1β composite score) at 12 months in patients receiving D+Q versus placebo. |
| methodology_notes | **Phase 1: Screening and Baseline Assessment (Weeks -4 to 0)** • Screen 200 potential participants aged 60-85 with mild cognitive impairment or early AD (CDR 0.5-1.0) • Confirm amyloid positivity via |
| replication_status | single_study |
| extraction_metadata | {'backfill_at': '2026-04-16T01:00:16.907038', 'needs_review': True, 'extraction_notes': 'Backfilled from wiki source (no PMID available)', 'extraction_confidence': 0.4} |
📊 Evidence Profile
Foundational
Evidence Balance
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Certainty
100%
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Incoming
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Outgoing
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derives from (16)
experiment-exp-wiki-experiment→hypothesis-h-3f02f222hypothesis-h-3f02f222→analysis-SDA-2026-04-01-gap-01analysis-SDA-2026-04-01-gap-01→hypothesis-h-3f02f222experiment-exp-wiki-experiment→hypothesis-h-58e4635ahypothesis-h-58e4635a→analysis-SDA-2026-04-01-gap-01
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analysis-SDA-2026-04-01-gap-01→hypothesis-h-58e4635aanalysis-SDA-2026-04-01-gap-01→hypothesis-h-cb833ed8analysis-SDA-2026-04-01-gap-01→hypothesis-h-1a34778fanalysis-SDA-2026-04-01-gap-01→hypothesis-h-bb518928experiment-exp-wiki-experiment→hypothesis-h-cb833ed8hypothesis-h-cb833ed8→analysis-SDA-2026-04-01-gap-01experiment-exp-wiki-experiment→hypothesis-h-1a34778fhypothesis-h-1a34778f→analysis-SDA-2026-04-01-gap-01experiment-exp-wiki-experiment→hypothesis-h-bb518928hypothesis-h-bb518928→analysis-SDA-2026-04-01-gap-01experiment-exp-wiki-experiment→wiki-experiments-senolytic-the
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