Amyloid-beta in Alzheimer's disease
- Primary identifiers
- 7
- Sponsors tracked
- 4
- Evidence types
- 2 of 3
- Last refreshed
- 2026-07-28 · monthly
MightyRayn panel synthesis
OmniRayn’s reading of this landscape — our interpretation, not a registry fact
Amyloid removal has become an engineering problem rather than a hypothesis, and the registry reads accordingly: the active studies are about dosing schedule, geography and prevention rather than whether clearance happens. The most useful item is a model-based meta-analysis across three antibodies showing that ARIA-E incidence tracks the RATE of plaque removal rather than exposure alone — which reframes the safety signal as a dial on the same mechanism that produces the benefit, not an unrelated toxicity. That is why a dedicated trial here studies dosing regimen against ARIA-E, and it is the constraint any new entrant inherits. Read alongside our tau landscape: the same platform trial shows plaque clearance leaves tangle biomarkers untouched.
Programs and primary evidence
| Sponsor | Asset | Phase | Mechanism | Primary source |
|---|---|---|---|---|
| Eli Lilly and Company | Donanemab (TRAILBLAZER) | 3 | anti-amyloid-beta monoclonal antibody |
|
| Eli Lilly and Company | Donanemab dosing regimens | 3 | dosing schedule as a lever on ARIA-E and amyloid lowering |
|
| Eli Lilly and Company | Donanemab (China) | 3 | anti-amyloid-beta monoclonal antibody |
|
| Washington University School of Medicine | Remternetug (DIAN-TU primary prevention) | 2/3 | anti-amyloid antibody in primary prevention |
|
| Washington University School of Medicine | Gantenerumab / solanezumab (DIAN-TU) | 2/3 | anti-amyloid antibodies with biomarker and cognitive endpoints |
|
| University of Miami (Baumel) | Mesenchymal stem cells added to anti-amyloid mAbs | 2 | adjunct to anti-amyloid monoclonal antibody therapy |
|
| AbbVie | model-based meta-analysis (not a preclinical study) | — | exposure-response linking plaque-removal rate to ARIA-E hazard |
|
Method and limits
- Programs are enumerated from primary registries (ClinicalTrials.gov, PubMed). A program appears here only if a primary record links this target to this indication as a therapeutic hypothesis — associations and risk markers are excluded by design.
- Every claim above carries the identifier it rests on. We report what the record states; we do not assert efficacy, and computational findings are pending wet-lab confirmation.
- Absence is not evidence of absence: unregistered, non-US and stealth-stage programs are not visible to these sources.
- This page refreshes monthly (no net-new primary entity in 74 days). Mechanism classifications are our reading of the public record and may be revised.
Want the analysis behind this landscape?
The public page is the map. The full dossier adds differentiation analysis, kill-tests and the whitespace read for this target — the parts we do not publish.