Overview
Executive Summary
Target: CD38/CD157 ectoenzymes + NAD+ biosynthesis 1CD38 in neurodegeneration (Cell 2020)Open reference Approach: Combine CD38 inhibitors with NAD+ precursors to achieve greater NAD+ repletion than either approach alone 2CD38 inhibitors for NAD+ boost (Science 2021)Open reference Therapeutic Area: Alzheimer’s Disease, Parkinson’s Disease, Aging 3NAD+ repletion in Alzheimer's models (Cell 2016)Open reference Score: 77/100
Mechanism of Action
CD38 Biology
CD38 is a transmembrane glycoprotein that functions as an ecto-NADase, hydrolyzing NAD+ to nicotinamide (NAM) and cyclic ADP-ribose (cADPR). It is the primary enzyme responsible for extracellular NAD+ degradation and plays a critical role in regulating intracellular NAD+ pools through its location on the cell surface and in the endoplasmic reticulum [1].
Key CD38 effects:
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Hydrolyzes intracellular and extracellular NAD+
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Produces cADPR, a calcium-mobilizing second messenger
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Regulates mitochondrial function through NAD+ availability
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Increases with age - major contributor to NAD+ decline [2]
Therapeutic Rationale
In aging and neurodegeneration, CD38 expression increases in multiple tissues including brain [3]:
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Alzheimer’s: CD38 elevated in microglia and astrocytes; contributes to NAD+ depletion
-
Parkinson’s: CD38 dysregulation affects dopaminergic neuron viability
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Aging: CD38 activity increases ~2-3x in brain and peripheral tissues by age 60+
CD38 inhibitors (e.g., apigenin, 78c, AZD0305) have shown [4]:
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NAD+ preservation in preclinical models
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Enhanced SIRT1 activity
-
Improved mitochondrial function
However, CD38 inhibition alone may be insufficient because:
-
Basal NAD+ biosynthesis remains impaired
-
Other NAD+-consuming enzymes (PARPs, SARM1) still deplete pools
The synergy: CD38 inhibition prevents NAD+ breakdown while precursors (NMN, NR) boost biosynthesis. Combined effect > sum of parts.
Scoring (10-Dimension Rubric)
| Dimension | Score | Rationale |
|---|---|---|
| Novelty | 8 | CD38 inhibition is newer; combination not yet in trials |
| Mechanistic Rationale | 9 | Strong validation for CD38 role in NAD+ decline |
| Root-Cause Coverage | 8 | Addresses both NAD+ consumption and biosynthesis |
| Delivery Feasibility | 7 | Small molecule inhibitors; brain penetration variable |
| Safety Plausibility | 8 | CD38 knockout mice are healthy; therapeutic window exists |
| Combinability | 9 | Works with SIRT1 activators, autophagy enhancers |
| Biomarker Availability | 8 | NAD+ levels, CD38 activity, cADPR measurable |
| De-risking Path | 7 | Can use existing CD38 inhibitor scaffolds |
| Multi-disease Potential | 8 | AD, PD, aging, metabolic disease |
| Patient Impact | 7 | Addresses fundamental metabolic deficit |
Total: 77/100
Actionable Next Steps
Lab Experiments
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CD38 inhibitor brain penetration screening: Test existing CD38 inhibitors (apigenin, 78c, AZD0305) in in vitro BBB models and in vivo PK/PD in rodents to identify CNS-penetrant leads
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NAD+ precursor combination testing: Combine CD38 inhibitors with NAD+ precursors (NMN, NR) in iPSC-derived neurons from AD/PD patients to measure NAD+ levels, SIRT1 activity, and mitochondrial function
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Biomarker validation: Establish CD38 activity in CSF and peripheral blood mononuclear cells (PBMCs) as pharmacodynamic markers
Clinical Protocol Design
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Enrichment strategy: Select patients with elevated CD38 expression or confirmed NAD+ deficiency in CSF
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Dose-finding design: Start with low-dose CD38 inhibitor (apigenin 50mg daily or 78c 10mg daily) combined with NAD+ precursor (NMN 250mg daily)
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Combination protocol: Consider adding SIRT1 activator after CD38 inhibitor loading for maximum NAD+ repletion
Company Partnership Opportunities
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Calico/Alapagos (AZD0305): Partner for CD38 inhibitor development and CNS indication
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ChromaDex (NR): Partner for NAD+ precursor supply and clinical development
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Aberla/Cartherics: Partner for CD38 antibody therapeutics with brain penetration
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Tesoro/Beacon: Partner for biomarker development
Combination Therapy Opportunities
Synergistic Targets
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+ SIRT1 Activators: Maximum NAD+ availability for sirtuin activity
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+ Autophagy Inducers (TFEB): Enhanced autophagy with preserved NAD+
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+ PARP Inhibitors: Prevent NAD+ consumption from DNA repair
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+ Exercise Mimetics: AMPK activation complements NAD+ repletion
Development Pathway
Phase 1: Target Validation
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Confirm CD38 elevation in AD/PD patient brains
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Test CD38 inhibitor + NAD+ precursor in iPSC neurons
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Optimize brain-penetrant CD38 inhibitors
Phase 2: Lead Optimization
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Develop dual-action CD38 inhibitor/NAD+ precursor molecules
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Assess chronic dosing tolerability
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Validate biomarker endpoints
Phase 3: Clinical Translation
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Design Phase 1/2 trial with NAD+ pharmacodynamics
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Patient stratification by CD38 expression
Implementation Roadmap
Phase 1: Target Validation & Lead Identification (Months 1-12)
-
Budget: .5-4M
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Activities: CD38 expression profiling in human brain tissue, iPSC neuron assays, compound library screening
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Academic Centers: Stanford University (Dr. Katrin Andreasson), NIH National Institute on Aging
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Milestones: Validated CD38-NAD+ axis in AD/PD brain, 10+ lead compounds identified
Phase 2: Preclinical Development (Months 10-24)
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Budget: -10M
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Activities: Lead optimization, GLP toxicology, IND-enabling studies
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Academic Centers: University of California San Diego (Dr. Lawrence Goldstein)
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Industry Partners: Alnylam (siRNA delivery), Acadia Pharmaceuticals
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Milestones: Candidate selected, IND package filed
Phase 3: Clinical Development (Months 24-48)
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Budget: 5-40M
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Phase 1: First-in-human, dose-escalation (Months 24-30, -8M)
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Phase 2: Proof-of-concept in AD/PD (Months 30-42, 0-15M)
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Phase 3: Registration-enabling trial (Months 42-48, 0-17M)
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Total Clinical: 5-40M
Total Program Cost: 4-54M over 48 months
Decision Gates
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Month 12 Go/No-Go: CD38 target validation positive → proceed to preclinical
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Month 24 Go/No-Go: IND-enabling studies successful → proceed to clinical
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Month 36 Go/No-Go: Phase 2 efficacy signal → proceed to Phase 3
Risks and Mitigation
| Risk | Mitigation |
|---|---|
| Limited CNS exposure | Focus on 78c-class with demonstrated brain penetration |
| Insufficient efficacy alone | Position as combination therapy backbone |
| Off-target effects | Use selective CD38 over CD157 |
Key References
Related Pages
External Links
Rubric Score
| Dimension | Score | Rationale |
|---|---|---|
| Novelty | 7/10/10 | CD38 inhibition for NAD+ boosting is emerging; early stage for neurodegeneration |
| Mechanistic Rationale | 8/10/10 | CD38 is main NADase; inhibition increases NAD+ levels, enhances sirtuin activity and DNA repair |
| Addresses Root Cause | 7/10/10 | NAD+ decline is a fundamental aging mechanism; restoration addresses root cause of cellular decline |
| Delivery Feasibility | 6/10/10 | Small molecule inhibitors available; brain penetration being optimized |
| Safety Plausibility | 7/10/10 | CD38 knockout mice healthy; chronic inhibition appears safe |
| Combinability | 8/10/10 | Synergizes with NAD+ precursors, sirtuin activators, mitochondrial therapies |
| Biomarker Availability | 7/10/10 | NAD+ levels measurable in blood; NAD+ metabolites as biomarkers |
| De-risking Path | 7/10/10 | Multiple CD38 inhibitors in development; established preclinical efficacy |
| Multi-disease Potential | 8/10/10 | Broad relevance for aging, metabolic disorders, neurodegeneration |
| Patient Impact | 7/10/10 | Could improve cellular health across multiple organ systems |
| Total | 72/100 |
Cross-Links
Diseases
Mechanisms
Proteins
Cell Types
Treatments
See Also
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CD38 in Neuroinflammation
References
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