{"artifact":{"id":"experiment-exp-wiki-experiments-senolytic-therapy-alzheimers-disease","artifact_type":"experiment","entity_ids":null,"title":"Senolytic Therapy (D+Q) Phase IIa Trial in Early Alzheimer's Disease","quality_score":0.675,"created_by":"crosslink-v2","provenance_chain":null,"content_hash":null,"metadata":{"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\n## Background and Rationale\nThis 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","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)**\n• Screen 200 potential participants aged 60-85 with mild cognitive impairment or early AD (CDR 0.5-1.0)\n• Confirm amyloid positivity via PET imaging (Centiloid >20) or CSF Aβ42/40 ratio <0.067\n• Obtain comprehensive neuropsychological battery (ADAS-Cog, MMSE, CDR-SB, FAQ)\n• Collect baseline blood biomarkers: p16INK4a, p21, IL-6, TNF-α, SASP factors\n• Perform baseline brain MRI with volumetric analysis and DTI sequences\n• Lumbar puncture for CSF collection: Aβ40, Aβ42, tau, p-tau181, neurofilament light\n• Randomize 120 eligible participants 1:1 to D+Q vs placebo arms (n=60 each)\n\n**Phase 2: Treatment Period (Weeks 1-24)**\n• Administer dasatinib 100mg + quercetin 1000mg orally for 2 consecutive days every 4 weeks (6 cycles total)\n• Placebo group receives matched capsules on same schedule\n• Safety monitoring every 2 weeks: CBC, comprehensive metabolic panel, liver enzymes\n• Cognitive assessments at weeks 4, 8, 12, 18, and 24\n•","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 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